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CompletedNCT04298879Updated Jun 5, 2024

IBI376 in Patients With Relapsed or Refractory Follicular Lymphoma/Marginal Zone Lymphoma

A Phase 2 interventional study of IBI376 in Indolent Non-hodgkin Lymphoma, sponsored by Innovent Biologics (Suzhou) Co. Ltd.. Completed at 1 site in China. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-06-05.

Sponsored by Innovent Biologics (Suzhou) Co. Ltd. · Phase 2, Interventional, and Treatment

Phase
Phase 2
Study type
Interventional
Enrollment
81
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

A Phase 2, Multicenter, Open-Label Study of IBI376, a PI3Kδ Inhibitor, in Patients with Relapsed or Refractory Follicular Lymphoma/Marginal Zone Lymphoma

Read the detailed description

Patients will be recruited for 2 cohorts. Cohort A will recruit 58 RRFL subjects, and Cohort B will recruit 62 RRMZL subjects.

02

Conditions studied

  • Indolent Non-hodgkin Lymphoma

Keywords

  • Follicular Lymphoma
  • Marginal Zone Lymphoma
  • Parsaclisib
03

In context

Lymphoma

5,578 studies on the registry are indexed under Lymphoma; 825 are open to participants now.

This study's enrollment of 81 is above the median of 40 across 4,508 interventional studies indexed under Lymphoma.

Browse Lymphoma studies →

Lead sponsor

Innovent Biologics (Suzhou) Co. Ltd. is the lead sponsor of 192 studies on the registry; 44 are open to participants now.

Of its 5 completed or terminated interventional studies of FDA-regulated products, 1 (20%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

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

Inclusion criteria

  1. Aged 18 years or older.
  2. Histologically confirmed, relapsed or refractory, follicular B-cell non-Hodgkin lymphoma (NHL) (FL) Grade 1, 2, and 3a or MZL.
  3. Ineligible for hematopoietic stem cell transplant.
  4. Definition of RRFL or RRMZL: Subjects should have received 2 or more prior therapies for FL/MZL included at least one regimen containing Rituximab. Subjects should be refractory to Rituximab or experienced disease progression after achieved remission or disease progression within 6 months since last therapy.
  5. Radiographically measurable lymphadenopathy or extranodal lymphoid malignancy (defined as the presence of ≥ 1 lesion that measures > 1.5 cm in the longest dimension and ≥ 1.0 cm in the longest perpendicular dimension as assessed by computed tomography (CT) or magnetic resonance imaging (MRI).
  6. Subjects must be willing to undergo an incisional, excisional, or core needle lymph node or tissue biopsy or provide a lymph node or tissue biopsy from the most recent available archival tissue.
  7. ECOG performance status 0 to 2.
  8. Life expectancy ≥ 12 weeks.
  9. Adequate hematologic, hepatic, and renal function.
  10. Willingness to avoid pregnancy or fathering children.

Exclusion criteria

Exclusion Criteria:

1 . Known histological transformation from indolent NHL to diffuse large B-cell lymphoma.

  1. History of central nervous system lymphoma (either primary or metastatic).
  1. Prior treatment with idelalisib, other selective PI3Kδ inhibitors, or a pan-PI3K inhibitor.
  1. Prior treatment with a Bruton's tyrosine kinase inhibitor (eg, ibrutinib).
  1. Allogeneic stem cell transplant within the last 6 months, or autologous stem cell transplant within the last 3 months before the date of study treatment administration.
  1. Active graft-versus-host disease. 7. Subjects positive for hepatitis B surface antigen or hepatitis B core antibody will be eligible if they are negative for HBV-DNA. Subjects positive for anti-HCV antibody will be eligible if they are negative for HCV-RNA.
05

Study design

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

Study arms

  • Experimental
    IBI376

    IBI376 will be administered orally at a dose of 20 mg once daily for 8 weeks followed by 2.5 mg once daily.

    Drug: IBI376

Interventions

  • DrugIBI376

    IBI376 20 mg po. once daily for 8 weeks ,followed by 2.5mg once daily

    Also known as: Parsaclisib

06

What researchers measure

Primary outcomes

  1. Objective Response Rate (ORR)

    To assess the efficacy of IBI376 in terms of objective response rate (ORR) in subjects with relapsed or refractory follicular lymphoma (FL)/Marginal lymphoma(MZL). Subjects will be evaluated for ORR by an IRC (Lugano criteria)

    Time frame: 2 years

Secondary outcomes

  1. Complete Response Rate (CRR)

    To assess complete response rate (CRR)

    Time frame: 2 years

  2. Duration of Response (DOR)

    To assess the duration of response (DOR)

    Time frame: 2 years

  3. Progression-free Survival (PFS)

    To assess progression-free survival (PFS)

    Time frame: 2 years

  4. Overall Survival (OS)

    To assess overall survival (OS)

    Time frame: 2 years

  5. Best percentage change in target lesion size

    To assess best percentage change in target lesion size

    Time frame: 2 years

  6. Safety and tolerability of IBI376 measured by adverse events (AEs)

    Defined as any AE either reported for the first time or worsening of a pre-existing event after first dose of study treatment.

    Time frame: Baseline through 30-35 days after end of treatment, up to approximately 12 months per subject

07

Study locations

1 site
  • Ruijin hospital, school of medicine, Shanghai jiao tong university
    Shanghai, China
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 5, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT04298879
Lead sponsor
Innovent Biologics (Suzhou) Co. Ltd.
Responsible party
Sponsor
First posted
Mar 6, 2020
Start date
Apr 7, 2020
Primary completion
Jul 27, 2021
Completion
Nov 21, 2023
Last update
Jun 5, 2024

Oversight

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

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This study is completed, as verified in Jun 2024. You cannot join it, but the record below documents what was studied.

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