CClinicalTrials.gg
CompletedNCT03484702TRANSCENDWORLDUpdated Dec 27, 2024Results posted

Trial to Determine the Efficacy and Safety of JCAR017 in Adult Participants With Aggressive B-Cell Non-Hodgkin Lymphoma

A Phase 2 interventional study of JCAR017 in Lymphoma, Non-Hodgkin, sponsored by Celgene. Completed at 20 sites in 11 countries. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-12-27.

Sponsored by Celgene · Phase 2, Interventional, and Treatment

Phase
Phase 2
Study type
Interventional
Enrollment
113
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

The purpose of this study is to evaluate the efficacy and safety of JCAR017 in participants with aggressive B-cell non-Hodgkin lymphoma (B-NHL)

Read the detailed description

This is a study to determine the efficacy and safety of JCAR017 in adult participants with aggressive B-cell NHL. The study will enroll participants in Europe and Japan with diffuse large B-cell lymphoma (DLBCL) not otherwise specified (NOS; de novo or transformed follicular lymphoma [tFL]), high-grade B-cell lymphoma with MYC and BCL2 and/or BCL6 rearrangements with DLBCL histology (HGBL), follicular lymphoma Grade 3B (FL3B), and primary central nervous system lymphoma (PCNSL). Participants with secondary central nervous system (CNS) involvement are allowed.

Once enrolled, participants will undergo leukapheresis to enable JCAR017 cell product generation. Upon successful JCAR017 cell product generation, participants will receive lymphodepleting chemotherapy followed by infusion of JCAR017. JCAR017 will be administered by intravenous infusion. Participants will be followed for approximately 2 years after their JCAR017 infusion for safety, disease status, survival and health-related quality of life.

Delayed adverse events following exposure to gene modified T cells will be assessed and long-term persistence of these modified T cells will continue to be monitored under a separate long-term follow-up protocol for up to 15 years after JCAR017 infusion as per competent authority guidelines.

02

Conditions studied

  • Lymphoma, Non-Hodgkin

Keywords

  • Non-Hodgkin lymphoma
  • Aggressive B-cell non-Hodgkin lymphoma
  • Diffuse large B-cell lymphoma
  • Relapse / refractory lymphoma
  • Transplant not eligible
  • High-grade B-cell lymphoma
  • Primary central nervous system lymphoma
  • Transformed follicular lymphoma
  • Follicular lymphoma Grade 3B
  • JCAR017
  • Liso-Cel
03

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Histological confirmation of diagnosis at last relapse
  • Adequate organ function
  • Adequate vascular access for leukapheresis procedure

Exclusion criteria

Exclusion Criteria:

  • Prior history of malignancies, other than aggressive relapsed/refractory Non-Hodgkin Lymphoma, unless the participant has been in remission for ≥ 2 years with the exception of non-invasive malignancies
  • Received previous CD19-targeted therapy
  • Progressive vascular tumor invasion, thrombosis, or embolism

Other protocol-defined inclusion/exclusion criteria apply

04

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
113 participants (actual)

Study arms

  • Experimental
    Administration of JCAR017

    Drug: JCAR017

Interventions

  • DrugJCAR017

    Specified dose on specified days

    Also known as: Lisocabtagene Maraleucel (liso-cel)

05

What researchers measure

Primary outcomes

  1. Overall Response Rate (ORR) Per Independent Review Committee in Cohorts 1, 2 and 3

    Overall response rate (ORR) by Independent Review Committee (Cohorts 1, 2, 3). ORR is the percent of participants with best overall response of complete response (CR) or partial response (PR). Complete response via PET-CT: * Lymph nodes/extralymphatic: Score 1, 2, 3a with/without residual mass on 5-point scale * New lesions: No * Bone marrow: No FDG-avid disease Complete response via CT scan: * Lymph nodes/extralymphatic: Target nodes/nodal masses ≤ 1.5 cm longest transverse diameter. * Nonmeasured lesion: No * New lesions: No * Bone marrow: Normal Partial response via PET-CT: * Lymph nodes/extralymphatic: Score 4, 5b, reduced uptake from baseline * New lesions: No * Bone marrow: Residual uptake higher than normal, reduced from baseline Partial response via CT scan: * Lymph nodes/extralymphatic: 50% decrease in sum of diameters of \<= 6 target measurable nodes/extranodal sites * Nonmeasured lesion: No * Organ enlargement: Spleen length decreased \> 50% * New lesions: No

    Time frame: From JCAR017 infusion until disease progression, end of study, the start of another anticancer therapy, or hemopoietic stem cell transplant (HSCT) (up to approximately 63 months)

  2. Overall Response Rate (ORR) Per Investigator in Cohort 4

    Overall response rate (ORR) is the percent of participants with best overall response of complete response (CR) or partial response (PR). Complete response via PET-CT: * Lymph nodes/extralymphatic: Score 1, 2, 3a with/without residual mass on 5-point scale * New lesions: No * Bone marrow: No FDG-avid disease Complete response via CT scan: * Lymph nodes/extralymphatic: Target nodes/nodal masses ≤ 1.5 cm longest transverse diameter. * Nonmeasured lesion: None * New lesions: No * Bone marrow: Normal Partial response via PET-CT: * Lymph nodes/extralymphatic: Score 4, 5b, reduced uptake from baseline * New lesions: None * Bone marrow: Residual uptake higher than normal, reduced from baseline Partial response via CT scan: * Lymph nodes/extralymphatic: 50% decrease in sum of diameters of \<= 6 target measurable nodes/extranodal sites * Nonmeasured lesion: None/normal * Organ enlargement: Spleen length decreased \> 50% * New lesions: No

    Time frame: From JCAR017 infusion until disease progression, end of study, the start of another anticancer therapy, or hemopoietic stem cell transplant (HSCT) (up to approximately 63 months)

  3. Overall Response Rate (ORR) Per Investigator in Cohort 5

    Overall response rate (ORR) determined by Investigator assessment after JCAR017 infusion. The ORR is the percent of participants with best overall response (BOR) of either complete response (CR), complete response unconfirmed (Cru) or partial response (PR). Complete response (CR): * Brain imaging: No contrast enhancement * Corticosteroid dose: None * Eye examination: Normal * Cerebrospinal fluid cytology: Negative Complete response unconfirmed (CRu): * Brain imaging: No contrast enhancement, Minimal abnormality * Corticosteroid dose: Any * Eye examination: Normal, minor RPE abnormality * Cerebrospinal fluid cytology: Negative Partial response (PR): * Brain imaging: 50% decrease in enhancing tumor, no contrast enhancement. * Corticosteroid dose: Irrelevant * Eye examination: Minor RPE abnormality, decrease in vitreous cells or retinal infiltrate. * Cerebrospinal fluid cytology: Negative, persistent or suspicious

    Time frame: From JCAR017 infusion until disease progression, end of study, the start of another anticancer therapy, or hemopoietic stem cell transplant (HSCT) (up to approximately 63 months)

  4. Number of Participants With Adverse Events in Cohort 7

    An adverse event (AE) is any noxious, unintended, or untoward medical occurrence that may appear or worsen in a participant during the course of a study. It may be a new intercurrent illness, a worsening concomitant illness, an injury, or any concomitant impairment of the participant's health, including laboratory test values, regardless of etiology. Any worsening (i.e., any clinically significant adverse change in the frequency or intensity of a preexisting condition) should be considered an AE. Graded according to NCI CTCAE (Version 4.03) guidelines where grade 1 = mild, grade 2 = moderate, grade 3 = severe, grade 4 = life threatening, grade 5 = death.

    Time frame: From leukapheresis to end of study (up to approximately 63 months)

  5. Number of Participants With Serious Adverse Events (SAEs) in Cohort 7

    A serious adverse event (SAE) is defined as any adverse event (AE) occurring at any dose that: * Results in death; * Is life-threatening (ie, in the opinion of the Investigator, the participant is at immediate risk of death from the AE); * Requires inpatient hospitalization or prolongation of existing hospitalization (hospitalization is defined as an inpatient admission, regardless of length of stay). * Results in persistent or significant disability/incapacity (a substantial disruption of the participant's ability to conduct normal life functions); * Is a congenital anomaly/birth defect; * Constitutes an important medical event. Graded according to NCI CTCAE (Version 4.03) guidelines where grade 1 = mild, grade 2 = moderate, grade 3 = severe, grade 4 = life threatening, grade 5 = death.

    Time frame: From leukapheresis to end of study (up to approximately 63 months)

  6. Number of Participants With Increase From Baseline in Select Hematology Parameters - Cohort 7

    JCAR017 treatment-emergent laboratory abnormalities are defined as an abnormality that, compared to baseline, worsens by at least one grade after JCAR017 infusion. The baseline value is defined as the last available recorded value on or prior to the date of JCAR017 infusion. Grade 1 (Mild), Grade 2 (Moderate), Grade 3 (Severe), Grade 4 (Life-threatening), Grade 5 (Death).

    Time frame: At Baseline and Day 29 after JCAR017 infusion

  7. Number of Participants With Increase From Baseline in Select Serum Chemistry Parameters - Cohort 7

    JCAR017 treatment-emergent laboratory abnormalities are defined as an abnormality that, compared to baseline, worsens by at least one grade after JCAR017 infusion. The baseline value is defined as the last available recorded value on or prior to the date of JCAR017 infusion. Grade 1 (Mild), Grade 2 (Moderate), Grade 3 (Severe), Grade 4 (Life-threatening), Grade 5 (Death).

    Time frame: At Baseline and Day 29 after JCAR017 infusion

Secondary outcomes

  1. Number of Participants With Adverse Events in Cohorts 1, 2, 3, 4, and 5

    An adverse event (AE) is any noxious, unintended, or untoward medical occurrence that may appear or worsen in a participant during the course of a study. It may be a new intercurrent illness, a worsening concomitant illness, an injury, or any concomitant impairment of the participant's health, including laboratory test values, regardless of etiology. Any worsening (i.e., any clinically significant adverse change in the frequency or intensity of a preexisting condition) should be considered an AE. Graded according to NCI CTCAE (Version 4.03) guidelines where grade 1 = mild, grade 2 = moderate, grade 3 = severe, grade 4 = life threatening, grade 5 = death.

    Time frame: From leukapheresis to end of study (up to approximately 63 months)

  2. Number of Participants With Serious Adverse Events (SAEs) in Cohorts 1, 2, 3, 4, and 5

    A serious adverse event (SAE) is defined as any adverse event (AE) occurring at any dose that: * Results in death; * Is life-threatening (ie, in the opinion of the Investigator, the participant is at immediate risk of death from the AE); * Requires inpatient hospitalization or prolongation of existing hospitalization (hospitalization is defined as an inpatient admission, regardless of length of stay). * Results in persistent or significant disability/incapacity (a substantial disruption of the participant's ability to conduct normal life functions); * Is a congenital anomaly/birth defect; * Constitutes an important medical event. Graded according to NCI CTCAE (Version 4) guidelines where grade 1 = mild, grade 2 = moderate, grade 3 = severe, grade 4 = life threatening, grade 5 = death.

    Time frame: From leukapheresis to end of study (up to approximately 63 months)

  3. Number of Participants With Increase From Baseline in Select Hematology Parameters - Cohorts 1, 2, 3, 4, and 5

    JCAR017 treatment-emergent laboratory abnormalities are defined as an abnormality that, compared to baseline, worsens by at least one grade after JCAR017 infusion. The baseline value is defined as the last available recorded value on or prior to the date of JCAR017 infusion. Grade 1 = Mild, Grade 2 =Moderate, Grade 3 =Severe, Grade 4 =Life-threatening, Grade 5 =Death.

    Time frame: At Baseline and Day 29 after JCAR017 infusion

  4. Number of Participants With Increase From Baseline in Select Serum Chemistry Parameters - Cohorts 1, 2, 3, 4, and 5

    JCAR017 treatment-emergent laboratory abnormalities are defined as an abnormality that, compared to baseline, worsens by at least one grade after JCAR017 infusion. The baseline value is defined as the last available recorded value on or prior to the date of JCAR017 infusion. Grade 1 = Mild, Grade 2 =Moderate, Grade 3 =Severe, Grade 4 =Life-threatening, Grade 5 =Death.

    Time frame: At Baseline and Day 29 after JCAR017 infusion

  5. Overall Response Rate (ORR) in Cohort 7

    ORR by Independent Review Committee. ORR is the percent of participants with best overall response of complete response (CR) or partial response (PR). Complete response via PET-CT: * Lymph nodes/extralymphatic: Score 1, 2, 3a with/without residual mass on 5-point scale * New lesions: No * Bone marrow: No FDG-avid disease Complete response via CT scan: * Lymph nodes/extralymphatic: Target nodes/nodal masses ≤ 1.5 cm longest transverse diameter. * Nonmeasured lesion: None * New lesions: No * Bone marrow: Normal Partial response via PET-CT: * Lymph nodes/extralymphatic: Score 4, 5b, reduced uptake from baseline * New lesions: None * Bone marrow: Residual uptake higher than normal, reduced from baseline Partial response via CT scan: * Lymph nodes/extralymphatic: 50% decrease in sum of diameters of \<= 6 target measurable nodes/extranodal sites * Nonmeasured lesion: None/normal * Organ enlargement: Spleen length decreased \> 50% * New lesions: No

    Time frame: From JCAR017 infusion until disease progression, end of study, the start of another anticancer therapy, or hemopoietic stem cell transplant (HSCT) (up to approximately 63 months)

  6. Complete Response Rate (CRR)

    Complete response rate is defined as percentage of participants achieving a best overall response of complete response. Complete response via PET-CT: * Lymph nodes/extralymphatic: Score 1, 2, 3a with/without residual mass on 5-point scale * New lesions: No * Bone marrow: No FDG-avid disease Complete response via CT scan: * Lymph nodes/extralymphatic: Target nodes/nodal masses ≤ 1.5 cm longest transverse diameter. * Nonmeasured lesion: None * New lesions: No * Bone marrow: Normal Complete response (CR) (Cohort 5): * Brain imaging: No contrast enhancement * Corticosteroid dose: None * Eye examination: Normal * Cerebrospinal fluid cytology: Negative Complete response unconfirmed (CRu) (Cohort 5): * Brain imaging: No contrast enhancement, Minimal abnormality * Corticosteroid dose: Any * Eye examination: Normal, minor RPE abnormality * Cerebrospinal fluid cytology: Negative

    Time frame: From JCAR017 infusion until disease progression, end of study, the start of another anticancer therapy, or hemopoietic stem cell transplant (HSCT) (up to approximately 63 months)

  7. Event Free Survival (EFS)

    Event-free survival is from JCAR017 infusion to death from any cause, progressive disease, or starting a new anticancer therapy. If a participant did not have an EFS event prior to data cutoff, EFS was censored at last disease assessment. Progressive disease (PD): * Target nodes/nodal masses: PPD progression. * Extranodal lesion: LDi \> 1.5 cm and increase by ≥ 50% from PPD nadir. * Splenomegaly: \> 50% of prior increase from baseline or by at least 2 cm from baseline. * Nonmeasured lesions: New or clear progression. * New lesions: Regrowth of previously resolved lesions. * Bone marrow: New or recurrent Progressive Disease (Cohort 5): * Brain imaging: \> 25% increase in enhancing lesion from baseline or best response. * Eye Exam: Increased vitreous cell counts or progressive retinal or optic nerve infiltration. * New lesion or site of disease

    Time frame: From JCAR017 infusion to death due to any reason, progressive disease, or starting a new anticancer therapy (up to approximately 63 months).

  8. Progression Free Survival (PFS) Using European Medicines Agency (EMA) Criteria

    Progression-free survival is defined as the interval from the date of JCAR017 infusion to progressive disease or death due to any cause, whichever occurred first. Per European Medicines Agency (EMA) criteria, participants who did not experience progressive disease and who did not die before the data cutoff date were censored at the time of the last visit with adequate response assessment when the participants were known not to have progressed. Estimated using Kaplan-Meier product-limit estimates.

    Time frame: From JCAR017 infusion to progressive disease or death due to any reason, whichever occurred first (up to approximately 63 months)

  9. Overall Survival (OS)

    Overall survival is defined as the interval from the date of JCAR017 infusion to the date of death due to any reason. Data from surviving participants was censored at the last time that the participant was known to be alive. Estimated using Kaplan-Meier product-limit estimates.

    Time frame: From the date of JCAR017 infusion to the date of death due to any reason (up to approximately 63 months).

  10. Duration of Response (DOR)

    DOR is from first response (complete response (CR), CR unconfirmed (CRu) or partial response (PR)) to progression (PD) or death. Those without PD or death were censored at the last assessment. CR via PET-CT: Lymph/extralymph: Score 1/2/3a w/w-out resid mass, no new lesions, No FDG-avid disease in bone marrow (BM) CR via CT scan: Lymph/extralymph: Target/nodal ≤ 1.5 cm, no new lesions, normal BM CR Cohort 5: No contrast enhance, no corticosteroid, normal eye exam, neg CSF cytology CRu Cohort 5: No contrast enhance, min abnorm, normal eye exam, neg CSF cytology PR via PET-CT: Lymph/extralymph: Score 4/5b, red uptake, no new lesions, resid uptake incr, reduced in BM PR via CT scan: Lymph/extralymph: 50% decr in sum of diam ≤ 6 target/extranodal, no new/nonmeasured lesions, Organ enlarge: Spleen decr \> 50% PR Cohort 5: 50% decr in enhancing tumor, no contrast enhance, Eye exam: Minor abnorm, decr in vitreous cells/retinal infiltrate, negative, persist or suspic CSF cytology.

    Time frame: From JCAR017 infusion until disease progression, death due to any reason, end of study, the start of another anticancer therapy, or hemopoietic stem cell transplant (HSCT) (up to approximately 63 months)

  11. Maximum Concentration (Cmax) of JCAR017 by qPCR

    Cmax is the maximum or peak concentration of drug reached in the plasma following a dose of the drug. Quantitative polymerase chain reaction (qPCR) was used to determine Cmax by detecting the JCAR017 transgene. Baseline is defined as the last available recorded value on or prior to the date of JCAR017 infusion.

    Time frame: At baseline and up until 24 months post JCAR017 infusion

  12. Time to Peak Concentration (Tmax) of JCAR017 by qPCR

    Time to maximum concentration (Tmax) is the time it takes for a drug to reach the maximum concentration (Cmax) after administration. Quantitative polymerase chain reaction (qPCR) was used to determine Tmax by detecting the JCAR017 transgene. Baseline is defined as the last available recorded value on or prior to the date of JCAR017 infusion.

    Time frame: At baseline and up until 24 months post JCAR017 infusion

  13. Total Exposure to JCAR017 as Measured by Area Under the Curve (AUC) of JCAR017 by qPCR

    Area Under the Curve (AUC) represents the total exposure of participants to study drug. Quantitative polymerase chain reaction (qPCR) was used to determine AUC by detecting the JCAR017 transgene. Baseline is defined as the last available recorded value on or prior to the date of JCAR017 infusion.

    Time frame: At baseline and up until 24 months post JCAR017 infusion

  14. Percent of Participants With Presence of JCAR017 Transgene in Peripheral Blood by qPCR

    Persistence is defined as a transgene count greater than or equal to the lower limit of detection (LLOD) of 5 copies per reaction. Data obtained after the start of a new anti-cancer therapy were excluded. qPCR = Quantitative polymerase chain reaction.

    Time frame: At Day 29 and Months 2, 3, 6, 9, 12, 18, and 24 post JCAR017 infusion.

  15. Change From Baseline in European Organisation for Research and Treatment of Cancer - Quality of Life C30 Questionnaire (EORTC QLQ-C30) Scores

    The EORTC QLQ-C30 consists of five functional scales (physical, role, emotional, cognitive, social), three symptom scales (fatigue, nausea/vomiting, pain), a global health status/health-related quality of life (HRQoL) scale, and six single items (dyspnea, insomnia, appetite loss, constipation, diarrhea, financial difficulties). The questionnaire is scored on a 4-point Likert scale: 1 = not at all, 2 = a little, 3 = quite a bit, 4 = very much. The raw score is the average of the items contributing to the scale. The final scores are calculated via linear transformation of raw scores and range from 0 to 100. For functional scales higher scores indicate better QoL. For symptom scales and single items lower scores indicate fewer symptoms, i.e. better QoL. Baseline the last available recorded scores on or prior to the date of JCAR017 infusion. Only global health, fatigue, physical and cognitive functioning subscales were assessed.

    Time frame: At baseline and Day 1, 29, 60, 90, 180, 270, 365, 545, and 730 post JCAR017 infusion.

  16. Change From Baseline in Functional Assessment of Cancer Treatment-Lymphoma "Additional Concerns" Subscale (FACT-LymS) Scores

    The Functional Assessment of Cancer Treatment-Lymphoma "Additional concerns" subscale (FACT-LymS) consists of the FACT-General scale and a 15-item lymphoma-specific additional concerns subscale (LYM). This scale addresses symptoms and functional limitations that are important to lymphoma patients. Only the LYM subscale was administered in this study. The LYM items are scored on a 0 ("Not at all") to 4 ("Very much") response scale. Items are aggregated to a single score on a 0-60 scale. Lower scores indicate better health outcomes. Baseline the last available recorded scores on or prior to the date of JCAR017 infusion.

    Time frame: At baseline and Day 1, 29, 60, 90, 180, 270, 365, 545, and 730 post JCAR017 infusion.

06

Results

Posted Dec 27, 2024

Participant flow

Pre-Treatment Period - Leukapheresis
Participant flow — Pre-Treatment Period - Leukapheresis
MilestoneCohort 1: Diffuse B-cell Lymphoma Who Failed ≥ 2 Lines of TherapyCohort 2: Transplant Ineligible Diffuse B-cell Lymphoma Who Failed First Line TherapyCohort 3: Japan Specific - Meeting Eligibility Criteria for Cohort 1 or 2Cohort 4: Newly Diagnosed High-Grade B-cell LymphomaCohort 5: Primary Central Nervous System LymphomaCohort 7: Meeting Cohort 1 Criteria Suitable for Treatment in an Outpatient Setting
Started4532144711
Completed4327121510
Not completed252321
Treatment Period
Participant flow — Treatment Period
MilestoneCohort 1: Diffuse B-cell Lymphoma Who Failed ≥ 2 Lines of TherapyCohort 2: Transplant Ineligible Diffuse B-cell Lymphoma Who Failed First Line TherapyCohort 3: Japan Specific - Meeting Eligibility Criteria for Cohort 1 or 2Cohort 4: Newly Diagnosed High-Grade B-cell LymphomaCohort 5: Primary Central Nervous System LymphomaCohort 7: Meeting Cohort 1 Criteria Suitable for Treatment in an Outpatient Setting
Started4327121510
Jcar017 treated set362710159
Completed392412159
Not completed430001
Withdrew: Death310000
Withdrew: Adverse event100000
Withdrew: Participant withdrew from study010000
Withdrew: Physician decision010001

Outcome measures

PrimaryOverall Response Rate (ORR) Per Independent Review Committee in Cohorts 1, 2 and 3

Overall response rate (ORR) by Independent Review Committee (Cohorts 1, 2, 3). ORR is the percent of participants with best overall response of complete response (CR) or partial response (PR). Complete response via PET-CT: * Lymph nodes/extralymphatic: Score 1, 2, 3a with/without residual mass on 5-point scale * New lesions: No * Bone marrow: No FDG-avid disease Complete response via CT scan: * Lymph nodes/extralymphatic: Target nodes/nodal masses ≤ 1.5 cm longest transverse diameter. * Nonmeasured lesion: No * New lesions: No * Bone marrow: Normal Partial response via PET-CT: * Lymph nodes/extralymphatic: Score 4, 5b, reduced uptake from baseline * New lesions: No * Bone marrow: Residual uptake higher than normal, reduced from baseline Partial response via CT scan: * Lymph nodes/extralymphatic: 50% decrease in sum of diameters of \<= 6 target measurable nodes/extranodal sites * Nonmeasured lesion: No * Organ enlargement: Spleen length decreased \> 50% * New lesions: No

Time frame:
From JCAR017 infusion until disease progression, end of study, the start of another anticancer therapy, or hemopoietic stem cell transplant (HSCT) (up to approximately 63 months)
Reported as:
Number · Percent of Participants
Overall Response Rate (ORR) Per Independent Review Committee in Cohorts 1, 2 and 3
Percent of ParticipantsCohort 1: Diffuse B-cell Lymphoma Who Failed ≥ 2 Lines of TherapyCohort 2: Transplant Ineligible Diffuse B-cell Lymphoma Who Failed First Line TherapyCohort 3: Japan Specific - Meeting Eligibility Criteria for Cohort 1 or 2
Overall Response Rate (ORR) Per Independent Review Committee in Cohorts 1, 2 and 361.1 (43.5 to 76.9)63.0 (42.4 to 80.6)70.0 (34.8 to 93.3)
PrimaryOverall Response Rate (ORR) Per Investigator in Cohort 4

Overall response rate (ORR) is the percent of participants with best overall response of complete response (CR) or partial response (PR). Complete response via PET-CT: * Lymph nodes/extralymphatic: Score 1, 2, 3a with/without residual mass on 5-point scale * New lesions: No * Bone marrow: No FDG-avid disease Complete response via CT scan: * Lymph nodes/extralymphatic: Target nodes/nodal masses ≤ 1.5 cm longest transverse diameter. * Nonmeasured lesion: None * New lesions: No * Bone marrow: Normal Partial response via PET-CT: * Lymph nodes/extralymphatic: Score 4, 5b, reduced uptake from baseline * New lesions: None * Bone marrow: Residual uptake higher than normal, reduced from baseline Partial response via CT scan: * Lymph nodes/extralymphatic: 50% decrease in sum of diameters of \<= 6 target measurable nodes/extranodal sites * Nonmeasured lesion: None/normal * Organ enlargement: Spleen length decreased \> 50% * New lesions: No

Time frame:
From JCAR017 infusion until disease progression, end of study, the start of another anticancer therapy, or hemopoietic stem cell transplant (HSCT) (up to approximately 63 months)
Reported as:
Number · Percent of Participants
Overall Response Rate (ORR) Per Investigator in Cohort 4
Percent of ParticipantsCohort 4: Newly Diagnosed High-Grade B-cell Lymphoma
Overall Response Rate (ORR) Per Investigator in Cohort 4100 (100 to 100)
PrimaryOverall Response Rate (ORR) Per Investigator in Cohort 5

Overall response rate (ORR) determined by Investigator assessment after JCAR017 infusion. The ORR is the percent of participants with best overall response (BOR) of either complete response (CR), complete response unconfirmed (Cru) or partial response (PR). Complete response (CR): * Brain imaging: No contrast enhancement * Corticosteroid dose: None * Eye examination: Normal * Cerebrospinal fluid cytology: Negative Complete response unconfirmed (CRu): * Brain imaging: No contrast enhancement, Minimal abnormality * Corticosteroid dose: Any * Eye examination: Normal, minor RPE abnormality * Cerebrospinal fluid cytology: Negative Partial response (PR): * Brain imaging: 50% decrease in enhancing tumor, no contrast enhancement. * Corticosteroid dose: Irrelevant * Eye examination: Minor RPE abnormality, decrease in vitreous cells or retinal infiltrate. * Cerebrospinal fluid cytology: Negative, persistent or suspicious

Time frame:
From JCAR017 infusion until disease progression, end of study, the start of another anticancer therapy, or hemopoietic stem cell transplant (HSCT) (up to approximately 63 months)
Reported as:
Number · Percent of Participants
Overall Response Rate (ORR) Per Investigator in Cohort 5
Percent of ParticipantsCohort 5: Primary Central Nervous System Lymphoma
Overall Response Rate (ORR) Per Investigator in Cohort 580.0 (28.4 to 99.5)
PrimaryNumber of Participants With Adverse Events in Cohort 7

An adverse event (AE) is any noxious, unintended, or untoward medical occurrence that may appear or worsen in a participant during the course of a study. It may be a new intercurrent illness, a worsening concomitant illness, an injury, or any concomitant impairment of the participant's health, including laboratory test values, regardless of etiology. Any worsening (i.e., any clinically significant adverse change in the frequency or intensity of a preexisting condition) should be considered an AE. Graded according to NCI CTCAE (Version 4.03) guidelines where grade 1 = mild, grade 2 = moderate, grade 3 = severe, grade 4 = life threatening, grade 5 = death.

Time frame:
From leukapheresis to end of study (up to approximately 63 months)
Reported as:
Count of participants · Participants
Number of Participants With Adverse Events in Cohort 7
ParticipantsCohort 7: Meeting Cohort 1 Criteria Suitable for Treatment in an Outpatient Setting
AEs occurring between leukapheresis and lymphodepleting chemotherapy (LDC)0
AEs occurring between LDC and JCAR017 infusion2
AEs occurring between JCAR017 infusion and Day 309
AEs occurring between Day 31 and Day 907
AEs occurring between Day 91 and end of study7
PrimaryNumber of Participants With Serious Adverse Events (SAEs) in Cohort 7

A serious adverse event (SAE) is defined as any adverse event (AE) occurring at any dose that: * Results in death; * Is life-threatening (ie, in the opinion of the Investigator, the participant is at immediate risk of death from the AE); * Requires inpatient hospitalization or prolongation of existing hospitalization (hospitalization is defined as an inpatient admission, regardless of length of stay). * Results in persistent or significant disability/incapacity (a substantial disruption of the participant's ability to conduct normal life functions); * Is a congenital anomaly/birth defect; * Constitutes an important medical event. Graded according to NCI CTCAE (Version 4.03) guidelines where grade 1 = mild, grade 2 = moderate, grade 3 = severe, grade 4 = life threatening, grade 5 = death.

Time frame:
From leukapheresis to end of study (up to approximately 63 months)
Reported as:
Count of participants · Participants
Number of Participants With Serious Adverse Events (SAEs) in Cohort 7
ParticipantsCohort 7: Meeting Cohort 1 Criteria Suitable for Treatment in an Outpatient Setting
SAEs occurring between leukapheresis and lymphodepleting chemotherapy (LDC)0
SAEs occurring between LDC and JCAR017 infusion0
SAEs occurring between JCAR017 infusion and Day 301
SAEs occurring between Day 31 and Day 900
SAEs occurring between Day 91 and end of study1
PrimaryNumber of Participants With Increase From Baseline in Select Hematology Parameters - Cohort 7

JCAR017 treatment-emergent laboratory abnormalities are defined as an abnormality that, compared to baseline, worsens by at least one grade after JCAR017 infusion. The baseline value is defined as the last available recorded value on or prior to the date of JCAR017 infusion. Grade 1 (Mild), Grade 2 (Moderate), Grade 3 (Severe), Grade 4 (Life-threatening), Grade 5 (Death).

Time frame:
At Baseline and Day 29 after JCAR017 infusion
Reported as:
Count of participants · Participants
Number of Participants With Increase From Baseline in Select Hematology Parameters - Cohort 7
ParticipantsCohort 7: Meeting Cohort 1 Criteria Suitable for Treatment in an Outpatient Setting
Leukocytes (10^9/L) - Day 290
Neutrophils, Segmented (10^9/L) - Day 292
Platelets (10^9/L) - Day 295
Activated Partial Thromboplastin Time (sec) - Day 290
Prothrombin Intl. Normalized Ratio - Day 291
PrimaryNumber of Participants With Increase From Baseline in Select Serum Chemistry Parameters - Cohort 7

JCAR017 treatment-emergent laboratory abnormalities are defined as an abnormality that, compared to baseline, worsens by at least one grade after JCAR017 infusion. The baseline value is defined as the last available recorded value on or prior to the date of JCAR017 infusion. Grade 1 (Mild), Grade 2 (Moderate), Grade 3 (Severe), Grade 4 (Life-threatening), Grade 5 (Death).

Time frame:
At Baseline and Day 29 after JCAR017 infusion
Reported as:
Count of participants · Participants
Number of Participants With Increase From Baseline in Select Serum Chemistry Parameters - Cohort 7
ParticipantsCohort 7: Meeting Cohort 1 Criteria Suitable for Treatment in an Outpatient Setting
Albumin (g/L) - Day 290
Phosphate (mmol/L) - Day 290
Alkaline Phosphatase (U/L) - Day 290
Alanine Aminotransferase (U/L) - Day 290
Aspartate Aminotransferase (U/L) - Day 291
Bilirubin (umol/L) - Day 290
Creatinine (umol/L) - Day 297
Triglycerides (mmol/L) - Day 293
Urate (umol/L) - Day 290
SecondaryNumber of Participants With Adverse Events in Cohorts 1, 2, 3, 4, and 5

An adverse event (AE) is any noxious, unintended, or untoward medical occurrence that may appear or worsen in a participant during the course of a study. It may be a new intercurrent illness, a worsening concomitant illness, an injury, or any concomitant impairment of the participant's health, including laboratory test values, regardless of etiology. Any worsening (i.e., any clinically significant adverse change in the frequency or intensity of a preexisting condition) should be considered an AE. Graded according to NCI CTCAE (Version 4.03) guidelines where grade 1 = mild, grade 2 = moderate, grade 3 = severe, grade 4 = life threatening, grade 5 = death.

Time frame:
From leukapheresis to end of study (up to approximately 63 months)
Reported as:
Count of participants · Participants
Number of Participants With Adverse Events in Cohorts 1, 2, 3, 4, and 5
ParticipantsCohort 1: Diffuse B-cell Lymphoma Who Failed ≥ 2 Lines of TherapyCohort 2: Transplant Ineligible Diffuse B-cell Lymphoma Who Failed First Line TherapyCohort 3: Japan Specific - Meeting Eligibility Criteria for Cohort 1 or 2Cohort 4: Newly Diagnosed High-Grade B-cell LymphomaCohort 5: Primary Central Nervous System Lymphoma
AEs occurring between leukapheresis and lymphodepleting chemotherapy (LDC)55000
AEs occurring between LDC and JCAR017 infusion2923804
AEs occurring between JCAR017 infusion and Day 3036261015
AEs occurring between Day 31 and Day 902510813
AEs occurring between Day 91 and end of study109702
SecondaryNumber of Participants With Serious Adverse Events (SAEs) in Cohorts 1, 2, 3, 4, and 5

A serious adverse event (SAE) is defined as any adverse event (AE) occurring at any dose that: * Results in death; * Is life-threatening (ie, in the opinion of the Investigator, the participant is at immediate risk of death from the AE); * Requires inpatient hospitalization or prolongation of existing hospitalization (hospitalization is defined as an inpatient admission, regardless of length of stay). * Results in persistent or significant disability/incapacity (a substantial disruption of the participant's ability to conduct normal life functions); * Is a congenital anomaly/birth defect; * Constitutes an important medical event. Graded according to NCI CTCAE (Version 4) guidelines where grade 1 = mild, grade 2 = moderate, grade 3 = severe, grade 4 = life threatening, grade 5 = death.

Time frame:
From leukapheresis to end of study (up to approximately 63 months)
Reported as:
Count of participants · Participants
Number of Participants With Serious Adverse Events (SAEs) in Cohorts 1, 2, 3, 4, and 5
ParticipantsCohort 1: Diffuse B-cell Lymphoma Who Failed ≥ 2 Lines of TherapyCohort 2: Transplant Ineligible Diffuse B-cell Lymphoma Who Failed First Line TherapyCohort 3: Japan Specific - Meeting Eligibility Criteria for Cohort 1 or 2Cohort 4: Newly Diagnosed High-Grade B-cell LymphomaCohort 5: Primary Central Nervous System Lymphoma
SAEs occurring between leukapheresis and lymphodepleting chemotherapy (LDC)01000
SAEs occurring between LDC and JCAR017 infusion10000
SAEs occurring between JCAR017 infusion and Day 30167001
SAEs occurring between Day 31 and Day 9073201
SAEs occurring between Day 91 and end of study53100
SecondaryNumber of Participants With Increase From Baseline in Select Hematology Parameters - Cohorts 1, 2, 3, 4, and 5

JCAR017 treatment-emergent laboratory abnormalities are defined as an abnormality that, compared to baseline, worsens by at least one grade after JCAR017 infusion. The baseline value is defined as the last available recorded value on or prior to the date of JCAR017 infusion. Grade 1 = Mild, Grade 2 =Moderate, Grade 3 =Severe, Grade 4 =Life-threatening, Grade 5 =Death.

Time frame:
At Baseline and Day 29 after JCAR017 infusion
Reported as:
Count of participants · Participants
Number of Participants With Increase From Baseline in Select Hematology Parameters - Cohorts 1, 2, 3, 4, and 5
ParticipantsCohort 1: Diffuse B-cell Lymphoma Who Failed ≥ 2 Lines of TherapyCohort 2: Transplant Ineligible Diffuse B-cell Lymphoma Who Failed First Line TherapyCohort 3: Japan Specific - Meeting Eligibility Criteria for Cohort 1 or 2Cohort 4: Newly Diagnosed High-Grade B-cell LymphomaCohort 5: Primary Central Nervous System Lymphoma
Leukocytes (10^9/L) - Day 2942101
Neutrophils, Segmented (10^9/L) - Day 29116301
Platelets (10^9/L) - Day 29138913
Activated Partial Thromboplastin Time (sec) - Day 2901101
Prothrombin Intl. Normalized Ratio - Day 2910000
SecondaryNumber of Participants With Increase From Baseline in Select Serum Chemistry Parameters - Cohorts 1, 2, 3, 4, and 5

JCAR017 treatment-emergent laboratory abnormalities are defined as an abnormality that, compared to baseline, worsens by at least one grade after JCAR017 infusion. The baseline value is defined as the last available recorded value on or prior to the date of JCAR017 infusion. Grade 1 = Mild, Grade 2 =Moderate, Grade 3 =Severe, Grade 4 =Life-threatening, Grade 5 =Death.

Time frame:
At Baseline and Day 29 after JCAR017 infusion
Reported as:
Count of participants · Participants
Number of Participants With Increase From Baseline in Select Serum Chemistry Parameters - Cohorts 1, 2, 3, 4, and 5
ParticipantsCohort 1: Diffuse B-cell Lymphoma Who Failed ≥ 2 Lines of TherapyCohort 2: Transplant Ineligible Diffuse B-cell Lymphoma Who Failed First Line TherapyCohort 3: Japan Specific - Meeting Eligibility Criteria for Cohort 1 or 2Cohort 4: Newly Diagnosed High-Grade B-cell LymphomaCohort 5: Primary Central Nervous System Lymphoma
Albumin (g/L) - Day 2900000
Phosphate (mmol/L) - Day 2901000
Alkaline Phosphatase (U/L) - Day 2921001
Alanine Aminotransferase (U/L) - Day 29103102
Aspartate Aminotransferase (U/L) - Day 2963103
Bilirubin (umol/L) - Day 2920000
Creatinine (umol/L) - Day 292320613
Triglycerides (mmol/L) - Day 29106202
Urate (umol/L) - Day 2910000
SecondaryOverall Response Rate (ORR) in Cohort 7

ORR by Independent Review Committee. ORR is the percent of participants with best overall response of complete response (CR) or partial response (PR). Complete response via PET-CT: * Lymph nodes/extralymphatic: Score 1, 2, 3a with/without residual mass on 5-point scale * New lesions: No * Bone marrow: No FDG-avid disease Complete response via CT scan: * Lymph nodes/extralymphatic: Target nodes/nodal masses ≤ 1.5 cm longest transverse diameter. * Nonmeasured lesion: None * New lesions: No * Bone marrow: Normal Partial response via PET-CT: * Lymph nodes/extralymphatic: Score 4, 5b, reduced uptake from baseline * New lesions: None * Bone marrow: Residual uptake higher than normal, reduced from baseline Partial response via CT scan: * Lymph nodes/extralymphatic: 50% decrease in sum of diameters of \<= 6 target measurable nodes/extranodal sites * Nonmeasured lesion: None/normal * Organ enlargement: Spleen length decreased \> 50% * New lesions: No

Time frame:
From JCAR017 infusion until disease progression, end of study, the start of another anticancer therapy, or hemopoietic stem cell transplant (HSCT) (up to approximately 63 months)
Reported as:
Number · Percent of Participants
Overall Response Rate (ORR) in Cohort 7
Percent of ParticipantsCohort 7: Meeting Cohort 1 Criteria Suitable for Treatment in an Outpatient Setting
Overall Response Rate (ORR) in Cohort 788.9 (51.8 to 99.7)
SecondaryComplete Response Rate (CRR)

Complete response rate is defined as percentage of participants achieving a best overall response of complete response. Complete response via PET-CT: * Lymph nodes/extralymphatic: Score 1, 2, 3a with/without residual mass on 5-point scale * New lesions: No * Bone marrow: No FDG-avid disease Complete response via CT scan: * Lymph nodes/extralymphatic: Target nodes/nodal masses ≤ 1.5 cm longest transverse diameter. * Nonmeasured lesion: None * New lesions: No * Bone marrow: Normal Complete response (CR) (Cohort 5): * Brain imaging: No contrast enhancement * Corticosteroid dose: None * Eye examination: Normal * Cerebrospinal fluid cytology: Negative Complete response unconfirmed (CRu) (Cohort 5): * Brain imaging: No contrast enhancement, Minimal abnormality * Corticosteroid dose: Any * Eye examination: Normal, minor RPE abnormality * Cerebrospinal fluid cytology: Negative

Time frame:
From JCAR017 infusion until disease progression, end of study, the start of another anticancer therapy, or hemopoietic stem cell transplant (HSCT) (up to approximately 63 months)
Reported as:
Number · Percent of Participants
Complete Response Rate (CRR)
Percent of ParticipantsCohort 1: Diffuse B-cell Lymphoma Who Failed ≥ 2 Lines of TherapyCohort 2: Transplant Ineligible Diffuse B-cell Lymphoma Who Failed First Line TherapyCohort 3: Japan Specific - Meeting Eligibility Criteria for Cohort 1 or 2Cohort 4: Newly Diagnosed High-Grade B-cell LymphomaCohort 5: Primary Central Nervous System LymphomaCohort 7: Meeting Cohort 1 Criteria Suitable for Treatment in an Outpatient Setting
Complete Response Rate (CRR)33.3 (18.6 to 51.0)48.1 (28.7 to 68.1)50.0 (18.7 to 81.3)0 (0 to 0)0 (0 to 0)88.9 (51.8 to 99.7)
SecondaryEvent Free Survival (EFS)

Event-free survival is from JCAR017 infusion to death from any cause, progressive disease, or starting a new anticancer therapy. If a participant did not have an EFS event prior to data cutoff, EFS was censored at last disease assessment. Progressive disease (PD): * Target nodes/nodal masses: PPD progression. * Extranodal lesion: LDi \> 1.5 cm and increase by ≥ 50% from PPD nadir. * Splenomegaly: \> 50% of prior increase from baseline or by at least 2 cm from baseline. * Nonmeasured lesions: New or clear progression. * New lesions: Regrowth of previously resolved lesions. * Bone marrow: New or recurrent Progressive Disease (Cohort 5): * Brain imaging: \> 25% increase in enhancing lesion from baseline or best response. * Eye Exam: Increased vitreous cell counts or progressive retinal or optic nerve infiltration. * New lesion or site of disease

Time frame:
From JCAR017 infusion to death due to any reason, progressive disease, or starting a new anticancer therapy (up to approximately 63 months).
Reported as:
Median · Months
Event Free Survival (EFS)
MonthsCohort 1: Diffuse B-cell Lymphoma Who Failed ≥ 2 Lines of TherapyCohort 2: Transplant Ineligible Diffuse B-cell Lymphoma Who Failed First Line TherapyCohort 3: Japan Specific - Meeting Eligibility Criteria for Cohort 1 or 2Cohort 4: Newly Diagnosed High-Grade B-cell LymphomaCohort 5: Primary Central Nervous System LymphomaCohort 7: Meeting Cohort 1 Criteria Suitable for Treatment in an Outpatient Setting
Event Free Survival (EFS)2.99 (2.60 to 5.22)3.12 (1.97 to 7.36)6.33 (0.56 to NA)23.95 (23.95 to 23.95)14.23 (0.76 to 24.02)NA (5.65 to NA)
SecondaryProgression Free Survival (PFS) Using European Medicines Agency (EMA) Criteria

Progression-free survival is defined as the interval from the date of JCAR017 infusion to progressive disease or death due to any cause, whichever occurred first. Per European Medicines Agency (EMA) criteria, participants who did not experience progressive disease and who did not die before the data cutoff date were censored at the time of the last visit with adequate response assessment when the participants were known not to have progressed. Estimated using Kaplan-Meier product-limit estimates.

Time frame:
From JCAR017 infusion to progressive disease or death due to any reason, whichever occurred first (up to approximately 63 months)
Reported as:
Median · Months
Progression Free Survival (PFS) Using European Medicines Agency (EMA) Criteria
MonthsCohort 1: Diffuse B-cell Lymphoma Who Failed ≥ 2 Lines of TherapyCohort 2: Transplant Ineligible Diffuse B-cell Lymphoma Who Failed First Line TherapyCohort 3: Japan Specific - Meeting Eligibility Criteria for Cohort 1 or 2Cohort 4: Newly Diagnosed High-Grade B-cell LymphomaCohort 5: Primary Central Nervous System LymphomaCohort 7: Meeting Cohort 1 Criteria Suitable for Treatment in an Outpatient Setting
Progression Free Survival (PFS) Using European Medicines Agency (EMA) Criteria2.99 (2.76 to 5.22)3.12 (1.97 to 7.36)6.33 (0.56 to NA)14.23 (0.76 to 24.02)23.95 (23.95 to 23.95)NA (5.65 to NA)
SecondaryOverall Survival (OS)

Overall survival is defined as the interval from the date of JCAR017 infusion to the date of death due to any reason. Data from surviving participants was censored at the last time that the participant was known to be alive. Estimated using Kaplan-Meier product-limit estimates.

Time frame:
From the date of JCAR017 infusion to the date of death due to any reason (up to approximately 63 months).
Reported as:
Mean · Months
Overall Survival (OS)
MonthsCohort 1: Diffuse B-cell Lymphoma Who Failed ≥ 2 Lines of TherapyCohort 2: Transplant Ineligible Diffuse B-cell Lymphoma Who Failed First Line TherapyCohort 3: Japan Specific - Meeting Eligibility Criteria for Cohort 1 or 2Cohort 4: Newly Diagnosed High-Grade B-cell LymphomaCohort 5: Primary Central Nervous System LymphomaCohort 7: Meeting Cohort 1 Criteria Suitable for Treatment in an Outpatient Setting
Overall Survival (OS)15.84 (5.82 to 23.95)16.82 (4.27 to NA)14.72 (1.71 to NA)31.74 (31.74 to 31.74)14.23 (4.30 to NA)NA (11.60 to NA)
SecondaryDuration of Response (DOR)

DOR is from first response (complete response (CR), CR unconfirmed (CRu) or partial response (PR)) to progression (PD) or death. Those without PD or death were censored at the last assessment. CR via PET-CT: Lymph/extralymph: Score 1/2/3a w/w-out resid mass, no new lesions, No FDG-avid disease in bone marrow (BM) CR via CT scan: Lymph/extralymph: Target/nodal ≤ 1.5 cm, no new lesions, normal BM CR Cohort 5: No contrast enhance, no corticosteroid, normal eye exam, neg CSF cytology CRu Cohort 5: No contrast enhance, min abnorm, normal eye exam, neg CSF cytology PR via PET-CT: Lymph/extralymph: Score 4/5b, red uptake, no new lesions, resid uptake incr, reduced in BM PR via CT scan: Lymph/extralymph: 50% decr in sum of diam ≤ 6 target/extranodal, no new/nonmeasured lesions, Organ enlarge: Spleen decr \> 50% PR Cohort 5: 50% decr in enhancing tumor, no contrast enhance, Eye exam: Minor abnorm, decr in vitreous cells/retinal infiltrate, negative, persist or suspic CSF cytology.

Time frame:
From JCAR017 infusion until disease progression, death due to any reason, end of study, the start of another anticancer therapy, or hemopoietic stem cell transplant (HSCT) (up to approximately 63 months)
Reported as:
Median · Months
Duration of Response (DOR)
MonthsCohort 1: Diffuse B-cell Lymphoma Who Failed ≥ 2 Lines of TherapyCohort 2: Transplant Ineligible Diffuse B-cell Lymphoma Who Failed First Line TherapyCohort 3: Japan Specific - Meeting Eligibility Criteria for Cohort 1 or 2Cohort 4: Newly Diagnosed High-Grade B-cell LymphomaCohort 5: Primary Central Nervous System LymphomaCohort 7: Meeting Cohort 1 Criteria Suitable for Treatment in an Outpatient Setting
Duration of Response (DOR)3.83 (2.07 to 17.05)3.91 (1.87 to NA)9.07 (2.04 to NA)17.97 (17.97 to 17.97)17.63 (2.46 to 23.10)NA (2.69 to NA)
SecondaryMaximum Concentration (Cmax) of JCAR017 by qPCR

Cmax is the maximum or peak concentration of drug reached in the plasma following a dose of the drug. Quantitative polymerase chain reaction (qPCR) was used to determine Cmax by detecting the JCAR017 transgene. Baseline is defined as the last available recorded value on or prior to the date of JCAR017 infusion.

Time frame:
At baseline and up until 24 months post JCAR017 infusion
Reported as:
Geometric mean · Copies/ug
Maximum Concentration (Cmax) of JCAR017 by qPCR
Copies/ugCohort 1: Diffuse B-cell Lymphoma Who Failed ≥ 2 Lines of TherapyCohort 2: Transplant Ineligible Diffuse B-cell Lymphoma Who Failed First Line TherapyCohort 3: Japan Specific - Meeting Eligibility Criteria for Cohort 1 or 2Cohort 4: Newly Diagnosed High-Grade B-cell LymphomaCohort 5: Primary Central Nervous System LymphomaCohort 7: Meeting Cohort 1 Criteria Suitable for Treatment in an Outpatient Setting
Maximum Concentration (Cmax) of JCAR017 by qPCR23132.1 ± 434.621960.0 ± 278.117337.8 ± 894.451121.0 ± NA7661.6 ± 1730.032027.1 ± 101.4
SecondaryTime to Peak Concentration (Tmax) of JCAR017 by qPCR

Time to maximum concentration (Tmax) is the time it takes for a drug to reach the maximum concentration (Cmax) after administration. Quantitative polymerase chain reaction (qPCR) was used to determine Tmax by detecting the JCAR017 transgene. Baseline is defined as the last available recorded value on or prior to the date of JCAR017 infusion.

Time frame:
At baseline and up until 24 months post JCAR017 infusion
Reported as:
Median · Days
Time to Peak Concentration (Tmax) of JCAR017 by qPCR
DaysCohort 1: Diffuse B-cell Lymphoma Who Failed ≥ 2 Lines of TherapyCohort 2: Transplant Ineligible Diffuse B-cell Lymphoma Who Failed First Line TherapyCohort 3: Japan Specific - Meeting Eligibility Criteria for Cohort 1 or 2Cohort 4: Newly Diagnosed High-Grade B-cell LymphomaCohort 5: Primary Central Nervous System LymphomaCohort 7: Meeting Cohort 1 Criteria Suitable for Treatment in an Outpatient Setting
Time to Peak Concentration (Tmax) of JCAR017 by qPCR11.6 (3.0 to 28.0)9.0 (7.0 to 14.0)84.1 (7.0 to 733.0)10.0 (10.0 to 10.0)9.0 (7.0 to 14.0)12.2 (10.0 to 21.0)
SecondaryTotal Exposure to JCAR017 as Measured by Area Under the Curve (AUC) of JCAR017 by qPCR

Area Under the Curve (AUC) represents the total exposure of participants to study drug. Quantitative polymerase chain reaction (qPCR) was used to determine AUC by detecting the JCAR017 transgene. Baseline is defined as the last available recorded value on or prior to the date of JCAR017 infusion.

Time frame:
At baseline and up until 24 months post JCAR017 infusion
Reported as:
Geometric mean · Days*copies/ug
Total Exposure to JCAR017 as Measured by Area Under the Curve (AUC) of JCAR017 by qPCR
Days*copies/ugCohort 1: Diffuse B-cell Lymphoma Who Failed ≥ 2 Lines of TherapyCohort 2: Transplant Ineligible Diffuse B-cell Lymphoma Who Failed First Line TherapyCohort 3: Japan Specific - Meeting Eligibility Criteria for Cohort 1 or 2Cohort 4: Newly Diagnosed High-Grade B-cell LymphomaCohort 5: Primary Central Nervous System LymphomaCohort 7: Meeting Cohort 1 Criteria Suitable for Treatment in an Outpatient Setting
Total Exposure to JCAR017 as Measured by Area Under the Curve (AUC) of JCAR017 by qPCR185586.667 ± 325.6157499.362 ± 211.9134819.085 ± 1268.9286119.439 ± NA64945.715 ± 1345.7199731.737 ± 136.8
SecondaryPercent of Participants With Presence of JCAR017 Transgene in Peripheral Blood by qPCR

Persistence is defined as a transgene count greater than or equal to the lower limit of detection (LLOD) of 5 copies per reaction. Data obtained after the start of a new anti-cancer therapy were excluded. qPCR = Quantitative polymerase chain reaction.

Time frame:
At Day 29 and Months 2, 3, 6, 9, 12, 18, and 24 post JCAR017 infusion.
Reported as:
Number · Percent of Participants
Percent of Participants With Presence of JCAR017 Transgene in Peripheral Blood by qPCR
Percent of ParticipantsCohort 1: Diffuse B-cell Lymphoma Who Failed ≥ 2 Lines of TherapyCohort 2: Transplant Ineligible Diffuse B-cell Lymphoma Who Failed First Line TherapyCohort 3: Japan Specific - Meeting Eligibility Criteria for Cohort 1 or 2Cohort 4: Newly Diagnosed High-Grade B-cell LymphomaCohort 5: Primary Central Nervous System LymphomaCohort 7: Meeting Cohort 1 Criteria Suitable for Treatment in an Outpatient Setting
Day 2988.295.2100.0100.080.0100.0
Month 270.066.7100.0100.0100.062.5
Month 361.550.0100.0100.0100.037.5
Month 633.345.571.40.0100.016.7
Month 941.740.060.00.0100.025.0
Month 1240.057.1100.00.066.70.0
Month 1825.057.175.00.0100.020.0
Month 2428.650.0100.00.0100.020.0
SecondaryChange From Baseline in European Organisation for Research and Treatment of Cancer - Quality of Life C30 Questionnaire (EORTC QLQ-C30) Scores

The EORTC QLQ-C30 consists of five functional scales (physical, role, emotional, cognitive, social), three symptom scales (fatigue, nausea/vomiting, pain), a global health status/health-related quality of life (HRQoL) scale, and six single items (dyspnea, insomnia, appetite loss, constipation, diarrhea, financial difficulties). The questionnaire is scored on a 4-point Likert scale: 1 = not at all, 2 = a little, 3 = quite a bit, 4 = very much. The raw score is the average of the items contributing to the scale. The final scores are calculated via linear transformation of raw scores and range from 0 to 100. For functional scales higher scores indicate better QoL. For symptom scales and single items lower scores indicate fewer symptoms, i.e. better QoL. Baseline the last available recorded scores on or prior to the date of JCAR017 infusion. Only global health, fatigue, physical and cognitive functioning subscales were assessed.

Time frame:
At baseline and Day 1, 29, 60, 90, 180, 270, 365, 545, and 730 post JCAR017 infusion.
Reported as:
Mean · Scores on a Scale
Change From Baseline in European Organisation for Research and Treatment of Cancer - Quality of Life C30 Questionnaire (EORTC QLQ-C30) Scores
Scores on a ScaleCohort 1: Diffuse B-cell Lymphoma Who Failed ≥ 2 Lines of TherapyCohort 2: Transplant Ineligible Diffuse B-cell Lymphoma Who Failed First Line TherapyCohort 3: Japan Specific - Meeting Eligibility Criteria for Cohort 1 or 2Cohort 4: Newly Diagnosed High-Grade B-cell LymphomaCohort 5: Primary Central Nervous System LymphomaCohort 7: Meeting Cohort 1 Criteria Suitable for Treatment in an Outpatient Setting
Global Health Status: Change from baseline Day 1-4.41 ± 17.070-5.07 ± 17.898-6.67 ± 10.244-8.33 ± NA8.33 ± 25.685-7.41 ± 12.108
Global Health Status: Change from baseline Day 29-1.26 ± 14.3010.00 ± 18.002-4.17 ± 17.2360.00 ± NA16.67 ± 11.785-1.85 ± 14.299
Global Health Status: Change from baseline Day 605.00 ± 14.7787.84 ± 17.5474.17 ± 16.4570.00 ± NA13.89 ± 26.7889.26 ± 8.784
Global Health Status: Change from baseline Day 902.47 ± 14.7661.28 ± 22.527-5.95 ± 17.8170.00 ± NA22.22 ± 41.1074.63 ± 8.448
Global Health Status: Change from baseline Day 1806.94 ± 13.6851.04 ± 23.332-13.10 ± 35.635-16.67 ± NA25.00 ± 22.0482.78 ± 8.607
Global Health Status: Change from baseline Day 2706.25 ± 20.1409.72 ± 9.742-3.33 ± 26.7450.00 ± NA25.00 ± 22.0483.33 ± 9.501
Global Health Status: Change from baseline Day 365-6.67 ± 20.3373.57 ± 11.664-12.50 ± 25.9090.00 ± NA30.56 ± 26.7883.33 ± 7.454
Global Health Status: Change from baseline Day 545-6.48 ± 18.5303.57 ± 26.726-5.56 ± 24.0560.00 ± NA0.00 ± 47.1401.67 ± 9.129
Global Health Status: Change from baseline Day 730-11.11 ± 12.975-4.17 ± 12.638-6.25 ± 7.9790.00 ± NA20.83 ± 29.463-2.08 ± 21.916
Physical Functioning: Change from baseline Day 1-3.33 ± 20.970-6.09 ± 21.074-3.33 ± 11.440-6.67 ± NA-2.67 ± 19.777-3.70 ± 14.948
Physical Functioning: Change from baseline Day 29-2.63 ± 18.555-4.21 ± 10.706-10.00 ± 14.8246.67 ± NA-8.33 ± 16.667-8.15 ± 18.493
Physical Functioning: Change from baseline Day 603.11 ± 15.135-0.39 ± 21.275-4.44 ± 15.5870.00 ± NA-2.22 ± 10.184-2.96 ± 10.062
Physical Functioning: Change from baseline Day 903.46 ± 16.7813.59 ± 12.054-5.71 ± 11.1746.67 ± NA11.11 ± 23.413-0.74 ± 18.692
Physical Functioning: Change from baseline Day 1807.78 ± 12.975-8.33 ± 31.219-5.71 ± 19.024-6.67 ± NA15.56 ± 27.756-2.22 ± 24.825
Physical Functioning: Change from baseline Day 2703.33 ± 10.0501.11 ± 19.052-2.67 ± 22.4106.67 ± NA24.44 ± 27.756-6.67 ± 31.972
Physical Functioning: Change from baseline Day 3650.67 ± 16.1630.95 ± 16.069-16.67 ± 20.0006.67 ± NA22.22 ± 26.9435.33 ± 11.926
Physical Functioning: Change from baseline Day 545-3.70 ± 26.690-1.90 ± 19.135-13.33 ± 23.0946.67 ± NA13.33 ± 47.1409.33 ± 11.155
Physical Functioning: Change from baseline Day 7301.11 ± 15.785-8.89 ± 28.493-3.33 ± 8.6076.67 ± NA3.33 ± 42.426-3.33 ± 11.547
Cognitive Functioning: Change from baseline Day 1-3.43 ± 17.301-3.62 ± 17.376-1.67 ± 9.4610.00 ± NA-3.33 ± 13.944-1.85 ± 10.015
Cognitive Functioning: Change from baseline Day 29-2.53 ± 16.2033.51 ± 14.2503.33 ± 13.1470.00 ± NA8.33 ± 21.517-7.41 ± 12.108
Cognitive Functioning: Change from baseline Day 602.78 ± 12.4440.98 ± 10.9780.00 ± 27.8890.00 ± NA33.33 ± 44.096-1.85 ± 13.029
Cognitive Functioning: Change from baseline Day 900.00 ± 13.074-1.28 ± 12.6594.76 ± 20.8930.00 ± NA11.11 ± 19.2450.00 ± 8.333
Cognitive Functioning: Change from baseline Day 180-2.78 ± 15.624-2.08 ± 5.89311.90 ± 20.8930.00 ± NA16.67 ± 28.868-5.56 ± 8.607
Cognitive Functioning: Change from baseline Day 2700.00 ± 22.4730.00 ± 0.0003.33 ± 13.9440.00 ± NA33.33 ± 44.0963.33 ± 7.454
Cognitive Functioning: Change from baseline Day 365-11.67 ± 22.2920.00 ± 0.000-4.17 ± 8.3330.00 ± NA22.22 ± 38.4906.67 ± 9.129
Cognitive Functioning: Change from baseline Day 545-7.41 ± 18.8402.38 ± 11.501-5.56 ± 19.2450.00 ± NA-41.67 ± 82.4963.33 ± 7.454
Cognitive Functioning: Change from baseline Day 730-1.39 ± 18.060-5.56 ± 8.607-4.17 ± 15.9570.00 ± NA-16.67 ± 23.570-4.17 ± 8.333
Fatigue: Change from baseline Day 11.63 ± 26.9591.45 ± 16.1733.33 ± 20.3200.00 ± NA-20.00 ± 30.8321.23 ± 18.794
Fatigue: Change from baseline Day 293.03 ± 24.4182.34 ± 12.0465.56 ± 17.568-11.11 ± NA-13.89 ± 27.7786.17 ± 14.815
Fatigue: Change from baseline Day 60-9.63 ± 18.623-1.31 ± 20.7433.70 ± 31.94611.11 ± NA-14.81 ± 35.7170.00 ± 17.568
Fatigue: Change from baseline Day 90-4.53 ± 19.795-4.27 ± 17.8814.76 ± 35.635-11.11 ± NA-37.04 ± 12.830-3.70 ± 22.906
Fatigue: Change from baseline Day 180-8.33 ± 21.2542.78 ± 34.503-4.76 ± 38.94622.22 ± NA-37.04 ± 23.1300.00 ± 33.702
Fatigue: Change from baseline Day 270-9.26 ± 15.5940.00 ± 22.222-6.67 ± 14.907-11.11 ± NA-29.63 ± 42.066-2.22 ± 34.605
Fatigue: Change from baseline Day 365-3.33 ± 14.861-4.76 ± 20.14113.89 ± 33.179-11.11 ± NA-44.44 ± 22.222-13.33 ± 14.487
Fatigue: Change from baseline Day 5454.94 ± 25.526-1.59 ± 19.698-3.70 ± 27.962-11.11 ± NA-5.56 ± 23.570-11.11 ± 15.713
Fatigue: Change from baseline Day 7300.93 ± 22.9473.70 ± 9.0725.56 ± 14.344-11.11 ± NA-16.67 ± 7.857-8.33 ± 16.667
SecondaryChange From Baseline in Functional Assessment of Cancer Treatment-Lymphoma "Additional Concerns" Subscale (FACT-LymS) Scores

The Functional Assessment of Cancer Treatment-Lymphoma "Additional concerns" subscale (FACT-LymS) consists of the FACT-General scale and a 15-item lymphoma-specific additional concerns subscale (LYM). This scale addresses symptoms and functional limitations that are important to lymphoma patients. Only the LYM subscale was administered in this study. The LYM items are scored on a 0 ("Not at all") to 4 ("Very much") response scale. Items are aggregated to a single score on a 0-60 scale. Lower scores indicate better health outcomes. Baseline the last available recorded scores on or prior to the date of JCAR017 infusion.

Time frame:
At baseline and Day 1, 29, 60, 90, 180, 270, 365, 545, and 730 post JCAR017 infusion.
Reported as:
Mean · Scores on a Scale
Change From Baseline in Functional Assessment of Cancer Treatment-Lymphoma "Additional Concerns" Subscale (FACT-LymS) Scores
Scores on a ScaleCohort 1: Diffuse B-cell Lymphoma Who Failed ≥ 2 Lines of TherapyCohort 2: Transplant Ineligible Diffuse B-cell Lymphoma Who Failed First Line TherapyCohort 3: Japan Specific - Meeting Eligibility Criteria for Cohort 1 or 2Cohort 4: Newly Diagnosed High-Grade B-cell LymphomaCohort 5: Primary Central Nervous System LymphomaCohort 7: Meeting Cohort 1 Criteria Suitable for Treatment in an Outpatient Setting
Change from baseline Day 10.7 ± 8.170.1 ± 7.051.9 ± 5.921.0 ± NA-4.0 ± 6.52-1.2 ± 11.08
Change from baseline Day 29-1.7 ± 7.14-2.7 ± 4.561.3 ± 7.24-4.0 ± NA-6.5 ± 8.101.0 ± 9.08
Change from baseline Day 60-2.8 ± 5.42-2.0 ± 4.20-3.3 ± 9.99-4.0 ± NA-4.7 ± 8.33-0.4 ± 9.95
Change from baseline Day 90-0.4 ± 5.42-2.8 ± 3.830.6 ± 9.25-5.0 ± NA-6.7 ± 8.50-1.7 ± 8.67
Change from baseline Day 1800.6 ± 5.14-1.8 ± 5.65-3.6 ± 10.202.0 ± NA-8.0 ± 7.001.0 ± 7.27
Change from baseline Day 270-0.3 ± 6.78-3.7 ± 2.25-1.0 ± 10.07-8.0 ± NA-10.00 ± 12.532.4 ± 5.22
Change from baseline Day 3651.3 ± 7.01-3.3 ± 3.302.0 ± 12.03-6.0 ± NA-6.7 ± 10.691.4 ± 7.33
Change from baseline Day 5450.7 ± 7.14-3.7 ± 4.35-4.7 ± 4.16-3.0 ± NA3.5 ± 6.36-1.0 ± 4.85
Change from baseline Day 7301.4 ± 7.12-0.8 ± 1.33-1.8 ± 5.32-2.0 ± NA-1.5 ± 12.02-1.5 ± 1.29

Adverse events

Collected over Participants were assessed for All-Cause Mortality, Serious Adverse Events and Other (Not Including Serious) Adverse Events from their date of leukapheresis until their study completion (assessed up to approximately 63 months).. Non-serious events are listed at a 5% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Cohort 1: Diffuse B-cell Lymphoma Who Failed ≥ 2 Lines of Therapy32/45 (71.1%)19/45 (42.2%)40/45 (88.9%)
Cohort 2: Transplant Ineligible Diffuse B-cell Lymphoma Who Failed First Line Therapy22/32 (68.8%)8/32 (25%)25/32 (78.1%)
Cohort 3: Japan Specific - Meeting Eligibility Criteria for Cohort 1 or 29/14 (64.3%)2/14 (14.3%)12/14 (85.7%)
Cohort 4: Newly Diagnosed High-Grade B-cell Lymphoma0/4 (0%)0/4 (0%)1/4 (25%)
Cohort 5: Primary Central Nervous System Lymphoma5/7 (71.4%)2/7 (28.6%)5/7 (71.4%)
Cohort 7: Meeting Cohort 1 Criteria Suitable for Treatment in an Outpatient Setting4/11 (36.4%)1/11 (9.1%)9/11 (81.8%)
Most frequent serious events
Showing 10 of 52
Most frequent serious events
EventCohort 1: Diffuse B-cell Lymphoma Who Failed ≥ 2 Lines of TherapyCohort 2: Transplant Ineligible Diffuse B-cell Lymphoma Who Failed First Line TherapyCohort 3: Japan Specific - Meeting Eligibility Criteria for Cohort 1 or 2Cohort 4: Newly Diagnosed High-Grade B-cell LymphomaCohort 5: Primary Central Nervous System LymphomaCohort 7: Meeting Cohort 1 Criteria Suitable for Treatment in an Outpatient Setting
Cytokine release syndromeImmune system disorders7/451/320/140/40/70/11
CystitisInfections and infestations0/450/320/140/41/70/11
SomnolenceNervous system disorders2/451/320/140/41/70/11
HaematuriaRenal and urinary disorders0/450/320/140/41/70/11
TremorNervous system disorders5/451/320/140/40/70/11
Confusional statePsychiatric disorders5/451/320/140/40/70/11
PyrexiaGeneral disorders1/450/320/140/40/71/11
Febrile neutropeniaBlood and lymphatic system disorders4/450/320/140/40/70/11
AphasiaNervous system disorders4/451/320/140/40/70/11
MelaenaGastrointestinal disorders0/450/321/140/40/70/11
Most frequent other events
Showing 10 of 59
Most frequent other events
EventCohort 1: Diffuse B-cell Lymphoma Who Failed ≥ 2 Lines of TherapyCohort 2: Transplant Ineligible Diffuse B-cell Lymphoma Who Failed First Line TherapyCohort 3: Japan Specific - Meeting Eligibility Criteria for Cohort 1 or 2Cohort 4: Newly Diagnosed High-Grade B-cell LymphomaCohort 5: Primary Central Nervous System LymphomaCohort 7: Meeting Cohort 1 Criteria Suitable for Treatment in an Outpatient Setting
NeutropeniaBlood and lymphatic system disorders35/4522/3211/141/45/79/11
LeukopeniaBlood and lymphatic system disorders9/455/3211/140/40/72/11
ThrombocytopeniaBlood and lymphatic system disorders16/4511/3211/141/43/73/11
AnaemiaBlood and lymphatic system disorders21/458/3210/140/43/72/11
PyrexiaGeneral disorders20/4510/322/140/42/71/11
Cytokine release syndromeImmune system disorders12/4512/326/140/43/70/11
HypofibrinogenaemiaBlood and lymphatic system disorders1/450/324/140/40/70/11
FatigueGeneral disorders3/451/324/140/40/71/11
HypogammaglobulinaemiaImmune system disorders6/453/324/140/40/70/11
Alanine aminotransferase increasedInvestigations2/450/320/140/42/70/11

Baseline characteristics

Age, Continuous
Age, Continuous(Years)Cohort 1: Diffuse B-cell Lymphoma Who Failed ≥ 2 Lines of TherapyCohort 2: Transplant Ineligible Diffuse B-cell Lymphoma Who Failed First Line TherapyCohort 3: Japan Specific - Meeting Eligibility Criteria for Cohort 1 or 2Cohort 4: Newly Diagnosed High-Grade B-cell LymphomaCohort 5: Primary Central Nervous System LymphomaCohort 7: Meeting Cohort 1 Criteria Suitable for Treatment in an Outpatient SettingTotal
Mean60.2 ± 10.6073.3 ± 5.5057.6 ± 10.0863.5 ± 21.1157.0 ± 5.7458.1 ± 12.4763.3 ± 11.56
Sex: Female, Male
Sex: Female, Male(Participants)Cohort 1: Diffuse B-cell Lymphoma Who Failed ≥ 2 Lines of TherapyCohort 2: Transplant Ineligible Diffuse B-cell Lymphoma Who Failed First Line TherapyCohort 3: Japan Specific - Meeting Eligibility Criteria for Cohort 1 or 2Cohort 4: Newly Diagnosed High-Grade B-cell LymphomaCohort 5: Primary Central Nervous System LymphomaCohort 7: Meeting Cohort 1 Criteria Suitable for Treatment in an Outpatient SettingTotal
Female1513613442
Male3019834771
Ethnicity (NIH/OMB)
Ethnicity (NIH/OMB)(Participants)Cohort 1: Diffuse B-cell Lymphoma Who Failed ≥ 2 Lines of TherapyCohort 2: Transplant Ineligible Diffuse B-cell Lymphoma Who Failed First Line TherapyCohort 3: Japan Specific - Meeting Eligibility Criteria for Cohort 1 or 2Cohort 4: Newly Diagnosed High-Grade B-cell LymphomaCohort 5: Primary Central Nervous System LymphomaCohort 7: Meeting Cohort 1 Criteria Suitable for Treatment in an Outpatient SettingTotal
Hispanic or Latino71010110
Not Hispanic or Latino29221425779
Unknown or Not Reported99012324
Race (NIH/OMB)
Race (NIH/OMB)(Participants)Cohort 1: Diffuse B-cell Lymphoma Who Failed ≥ 2 Lines of TherapyCohort 2: Transplant Ineligible Diffuse B-cell Lymphoma Who Failed First Line TherapyCohort 3: Japan Specific - Meeting Eligibility Criteria for Cohort 1 or 2Cohort 4: Newly Diagnosed High-Grade B-cell LymphomaCohort 5: Primary Central Nervous System LymphomaCohort 7: Meeting Cohort 1 Criteria Suitable for Treatment in an Outpatient SettingTotal
American Indian or Alaska Native0000000
Asian031400017
Native Hawaiian or Other Pacific Islander0000000
Black or African American0000000
White3719035771
More than one race0000000
Unknown or Not Reported810012425
07

Study locations

20 sites
  • Local Institution - 101
    Wien, 1090, Austria
  • Local Institution - 351
    Gent, 9000, Belgium
  • Local Institution - 551
    Helsinki, 00029, Finland
  • Local Institution - 202
    Lille, 59037, France
  • Local Institution - 203
    Paris Cedex 10, 75475, France
  • Local Institution - 201
    Pierre Benite cedex, 69495, France
  • Local Institution - 152
    Dresden, 01307, Germany
  • Local Institution - 155
    Heidelberg, 69120, Germany
  • Local Institution - 151
    Köln, 50937, Germany
  • Local Institution - 154
    München, 81377, Germany
  • Local Institution - 153
    Ulm, 89081, Germany
  • Local Institution - 402
    Milan, 20133, Italy
  • Local Institution - 401
    Torino, 10126, Italy
  • Local Institution - 601
    Chuo-ku, Tokyo 104-0045, Japan
  • Local Institution - 602
    Minato-ku, Tokyo 105-8470, Japan
  • Local Institution - 301
    Rotterdam, 3015 CE, Netherlands
  • Local Institution - 451
    Barcelona, 08035, Spain
  • Local Institution - 251
    Bern, 3010, Switzerland
  • Local Institution - 502
    Manchester, Lancashire M20 4BX, United Kingdom
  • Local Institution - 501
    London, WC1E 6BT, United Kingdom
08

References and documents

Publications

  • Ernst M, Oeser A, Besiroglu B, Caro-Valenzuela J, Abd El Aziz M, Monsef I, Borchmann P, Estcourt LJ, Skoetz N, Goldkuhle M. Chimeric antigen receptor (CAR) T-cell therapy for people with relapsed or refractory diffuse large B-cell lymphoma. Cochrane Database Syst Rev. 2021 Sep 13;9(9):CD013365. doi: 10.1002/14651858.CD013365.pub2. PubMed 34515338 ↗

Study documents

  • Protocol and statistical analysis plan · Aug 12, 2021

Documents are hosted by the registry — open the source record to download them.

09

Registry details

Key details

Study ID
NCT03484702
Lead sponsor
Celgene
Responsible party
Sponsor
First posted
Apr 2, 2018
Start date
Jun 5, 2018
Primary completion
Dec 15, 2023
Completion
Dec 15, 2023
Results posted
Dec 27, 2024
Last update
Dec 27, 2024

Study contacts

Bristol-Myers Squibb
study director · Bristol-Myers Squibb

Oversight

Data monitoring committee
Yes
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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