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Not yet recruitingNCT07905261Updated Oct 29, 2026

Clinical Study of SYS6055 Injection in Participants With Relapsed/Refractory B-Cell Non-Hodgkin Lymphoma

A Phase 1/2 interventional study of SYS6055 in Relapsed/Refractory B-Cell Non-Hodgkin Lymphoma, sponsored by Beijing Kangchuanglian Biopharmaceutical Technology Research Co., Ltd. Not yet recruiting. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-10-29.

Sponsored by Beijing Kangchuanglian Biopharmaceutical Technology Research Co., Ltd · Phase 1/2, Interventional, and Treatment

Updated Oct 29, 2026Newly registeredGo to Updates ↓
Phase
Phase 1/2
Study type
Interventional
Enrollment
384
Allocation
Non-randomized
Ages
18 Years and older
Sex
All
01

Study summary

This is a Phase I/II clinical study conducted in participants with relapsed/refractory B-Cell Non-Hodgkin Lymphoma. The study aims to evaluate the safety, tolerability, pharmacokinetic characteristics and preliminary efficacy of SYS6055 Injection in participants with relapsed/refractory aggressive B-cell lymphoma, and to provide a basis for the recommended dosing regimen in subsequent studies.

02

Conditions studied

  • Relapsed/Refractory B-Cell Non-Hodgkin Lymphoma

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03

In context

Lymphoma, B-Cell

885 studies on the registry are indexed under Lymphoma, B-Cell; 286 are open to participants now.

This study's planned enrollment of 384 is above the median of 34 across 773 interventional studies indexed under Lymphoma, B-Cell.

Browse Lymphoma, B-Cell studies →

Lead sponsor

Beijing Kangchuanglian Biopharmaceutical Technology Research Co., Ltd is the lead sponsor of 3 studies on the registry; 3 are open to participants now.

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

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age ≥ 18 year, and voluntarily signed the Form (ICF);
  • confirmed B-cell non-Hodgkin lymphoma (defined according to the 5th edition of the WHO classification), pathological subtypes include large B-cell lymphoma and others.
  • Pathologically confirmed positive expression of CD19 antigen on tumor cells.
  • Participants with B-cell non-Hodgkin lymphoma after failure of standard treatment.
  • At least one according to the 2014 Lugano Response Criteria for Lymphoma;
  • performance status score of 0-1;
  • Expected survival of at least 3 months;
  • Adequate organ and bone marrow function;
  • Eligible participants (males and females) of must agree to use a reliable method of (hormonal contraception, barrier method, or abstinence) with their partner during the trial and for at least 1 year after dosing. Female participants of must have a negative serum pregnancy test within 7 days prior to enrollment. In addition, female participants must agree not to donate oocytes (eggs, ova) for assisted reproductive technology for 1 year after dosing, and male participants must agree not to donate sperm for assisted reproductive technology for 1 year after dosing;
  • Willing and able to comply with scheduled visits, treatment plan, laboratory tests, and other study procedures.

Exclusion criteria

Exclusion Criteria:

  • History of other within 3 years or concurrent other active malignancy (participants with cured localized tumors such as basal cell carcinoma of the skin, squamous cell carcinoma of the skin, superficial bladder cancer, carcinoma in situ of the prostate, carcinoma in situ of the cervix, carcinoma in situ of the breast, etc., may be enrolled);
  • Participants with bleeding diathesis, active bleeding, hemoptysis, or history of major bleeding within the previous 6 months; tumor invasion of major blood vessels shown by imaging (CT or MRI), or tumor judged by the investigator as highly likely to invade major blood vessels and cause fatal massive bleeding during the subsequent study period;
  • Participants with B-cell non-Hodgkin lymphoma involving the central nervous system;
  • Received hematopoietic stem cell transplantation within 3 months prior to the first dose;
  • Previous allogeneic bone marrow transplantation, gene therapy, or adoptive cell therapy (including CAR-T therapy);
  • Received , anti-PD-L1, or T-cell engager therapy within 3 months prior to the first dose; received fludarabine or bendamustine within 6 months prior to the first dose;
  • Adverse events from prior antineoplastic therapy have not recovered to Version 6.0 grade ≤1 (except for alopecia or other toxicities without safety risk as judged by the investigator);
  • Other prior therapies:Major surgery or curative radiotherapy within 28 days prior to dosing; Antibody-based targeted therapy or immunotherapy within 28 days or 5 half-lives (whichever is shorter) prior to dosing; Palliative radiotherapy within 14 days prior to dosing; Chemotherapy or small-molecule targeted therapy within 14 days or 5 half-lives (whichever is shorter) prior to dosing
  • Simultaneously participating in another clinical trial, unless it is an observational (non-interventional) clinical trial or in the follow-up phase of an interventional trial (without impact on the follow-up data of this study);
  • Received within 4 weeks prior to dosing;
  • Active bacterial, fungal, or viral infection prior to dosing. Individuals receiving prophylactic antimicrobial therapy without clinical manifestations of active infection prior to dosing may be considered for enrollment;
  • disease requiring systemic therapy;
  • History of central nervous system disease or current persistent central nervous system disease that may interfere with neurological assessments;
  • History of immunodeficiency or positive antibody test during screening;
  • History of tuberculosis treatment within 2 years prior to dosing; history of active syphilis;
  • Active or during screening. Active hepatitis B is defined as HBsAg-positive and HBV DNA > ; Active hepatitis C is defined as HCV antibody-positive and HCV RNA > ULN;
  • History of severe cardiovascular disease;
  • or intolerance to of SYS6055 (primarily human serum albumin) or reconstitution solvent (with 5% human serum albumin).
  • Any other conditions in participants that may interfere with compliance with study procedures, are not in the best interest of participants, or may affect study results: e.g., history of psychiatric disorders, drug addiction or substance abuse, any other diseases or conditions, etc.;
  • Pregnant or lactating female;
  • Any other reason judged by the investigator that the participant is not suitable for participation in this clinical trial.
Terms in these criteria, in plain language(21)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

Histologically or cytologically confirmed

The diagnosis was confirmed by looking at a sample under a microscope: tissue from a biopsy or surgery (histology), or cells from a fluid or needle sample (cytology).

Your pathology report is the document that shows this.

Relapsed and refractory

Relapsed: the illness came back after treatment had worked. Refractory: it did not respond to treatment, or stopped responding while still on it.

Measurable disease

The amount of disease can be tracked with a defined measurement, so the study can see whether it shrinks or grows. It might be a tumour measured on a scan or, in some blood cancers such as myeloma, a marker measured in blood or urine.

The criteria or the study team say which measurement counts — having no tumour visible on a scan does not by itself rule you out.

ECOG performance status

A scale of how much an illness limits everyday activity. For people being assessed to join a study, scores run from 0 (fully active) to 4; lower is more active.

0
Fully active, no restrictions.
1
Limited in strenuous activity, but walking and able to do light work, such as housework or office work.
2
Walking and able to look after yourself, but unable to work; up and about more than half of waking hours.
3
Able to look after yourself only in part; in bed or a chair more than half of waking hours.
4
Unable to look after yourself at all; in bed or a chair all day.

Studies most often ask for 0–1 or 0–2. Your doctor gives the score; the WHO scale uses the same steps. The full scale also has 5, which records death.

Reproductive potential

Able to have children. For women this usually means from the first period until menopause, unless permanently unable to through surgery; for men, unless permanently sterile. Read who the line is about — participants, women, men, or their partners.

Criteria about it usually ask for contraception during the study and for a time after it.

Contraception

Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.

Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.

Childbearing potential

Able to become pregnant: from the first period until menopause, unless permanently unable to through surgery (removal of the womb, or of both ovaries or both fallopian tubes).

Criteria for people of childbearing potential usually ask for a negative pregnancy test and for contraception during the study and for a time after it.

Cancer (malignancy)

Malignancy means cancer. Criteria about another or earlier malignancy ask whether you have had a different cancer, usually within a set number of years.

Some are commonly allowed, such as treated skin cancers other than melanoma and early cancers removed completely — check the exceptions this study lists.

Allogeneic and autologous transplant

Stem cell (bone marrow) transplants. Allogeneic uses cells from a donor; autologous uses your own cells, collected earlier and given back.

PD-1, PD-L1 and checkpoint inhibitors

PD-1, PD-L1 and CTLA-4 are proteins that act as brakes on the immune system. Checkpoint inhibitors, such as pembrolizumab or nivolumab, block them so the immune system can attack a cancer.

PD-L1 can also be measured in a tumour sample. Some scores count stained tumour cells only (TPS); others also count certain immune cells (CPS). The study names the score and the minimum it uses.

CTCAE grade

The US National Cancer Institute’s scale of how severe an adverse event is — any unwanted medical event during a study, such as a symptom, an illness or an abnormal test result, whether or not a treatment caused it. Whether it did is judged separately.

1
Mild.
2
Moderate.
3
Severe.
4
Life-threatening.
5
Death due to the event.

“Side effects of earlier treatment resolved to grade 1 or less” means they have settled to mild or gone.

Live vaccines

Vaccines made with a weakened form of the germ, such as measles–mumps–rubella (MMR), chickenpox and yellow fever. They can be risky when the immune system is weakened. Flu injections are not live; the nasal flu spray is.

Autoimmune disease

A condition in which the immune system attacks the body’s own tissues, such as rheumatoid arthritis, lupus, psoriasis, type 1 diabetes or inflammatory bowel disease.

Immunotherapy studies often leave out active autoimmune disease, and some name exceptions, such as thyroid disease on replacement hormone. Check the exceptions this study lists.

HIV

The human immunodeficiency virus, which weakens the immune system.

Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.

Hepatitis B tests

Hepatitis B is a virus that infects the liver. These are separate tests: HBsAg positive usually means a current infection (a recent vaccination can briefly cause it too); total anti-HBc (HBcAb) positive means an infection now or in the past; HBV DNA measures how much virus is in the blood.

Some studies accept a past infection if HBV DNA is undetectable, sometimes with antiviral medicine during the study. Check what this study allows.

Hepatitis C tests

Hepatitis C is a virus that infects the liver. An HCV antibody test can stay positive after an infection has cleared (and is occasionally positive without one); an HCV RNA test shows whether the virus is there now.

After treatment, hepatitis C counts as cured when HCV RNA is still undetectable 12 weeks or more after the treatment ended. Studies often accept people cured this way.

ULN (upper limit of normal)

The top of the normal range for a blood test, as set by the laboratory that runs it. Each lab prints its own range next to your result.

“≤ 2.5 × ULN” means the result can be up to two and a half times that top value.

Hypersensitivity

An allergy, or another reaction of the immune system, to a substance. “Hypersensitivity to the study drug” means a known allergic reaction to it — not every side effect a medicine can have.

Excipients

The other ingredients in a medicine besides the active drug, such as fillers, colours or preservatives.

Clinically significant

Judged by the study doctor to matter for your health or for the study. It is a doctor’s decision, so ask the study team if you are unsure whether something counts.

05

Study design

Phase
Phase 1 / Phase 2
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Single group
Masking
None (open label)
Enrollment
384 participants (estimated)

Study arms

  • Experimental
    Dose Escalation, Backfill and Cohort Expansion

    In the dose-escalation phase, participants will receive escalating doses of SYS6055. In the backfill and cohort expansion phase, participants will receive selected doses of SYS6055. Participants will be administered a single dose on Day 0 of Cycle 1.

    Drug: SYS6055

Interventions

  • The dose will be selected based on the dose cohort, with a single administration.

06

What researchers measure

Primary outcomes

  1. Dose-limiting toxicities (DLTs)

    Time frame: Dose-limiting toxicities (DLTs) will be assessed 28 days after the first dose.

  2. Occurrence of Adverse Events (AE)

    Time frame: Up to 24 months after administration of 6055

  3. Occurrence of Serious Adverse Events (SAE)

    Time frame: Up to 24 months after administration of 6055

  4. Recommended Phase 2 Dose (RP2D) of SYS6055

    Time frame: through study completion, an average of 3 years

  5. Maximum Tolerated Dose (MTD) of SYS6055

    Time frame: through study completion, an average of 3 years

Secondary outcomes

  1. Objective Response Rate (ORR)

    Time frame: through study completion, an average of 3 years

  2. Time to Response(TTR )

    Time frame: through study completion, an average of 3 years

  3. Duration of Response (DoR)

    Time frame: through study completion, an average of 3 years

  4. Progression-free survival (PFS)

    Time frame: through study completion, an average of 3 years

  5. Overall Survival (OS)

    Time frame: through study completion, an average of 3 years

  6. PK, CD19-CAR copy number and CD19 CAR-T cell content of SYS6055

    The levels of CD19 CAR RNA and DNA in peripheral blood will be determined by qPCR, with the proportion of CD19 CAR-T cells assessed by flow cytometry.

    Time frame: 2 years

  7. PK, CD19 CAR-T cell phenotypes

    CD19 CAR-T cell phenotypes will be analyzed by flow cytometry, including CD4/CD8 ratio, naïve cells, memory cells, and effector cells.

    Time frame: 2 years

  8. PD

    Levels of cytokines in peripheral blood (IL-6, IL-10, IFN-γ, TNF-α, etc.).

    Time frame: 2 years

  9. PD

    CRP

    Time frame: 2 years

  10. PD

    ferritin levels

    Time frame: 2 years

  11. PD

    immunoglobulin levels (IgG, IgA, IgM)

    Time frame: 2 years

  12. PD

    peripheral blood lymphocyte subsets (proportion of T, B, and NK cells),Lymphocyte subsets will be analyzed by flow cytometry.

    Time frame: 2 years

  13. PD

    peripheral blood lymphocyte subsets (absolute counts of T, B, and NK cells). Lymphocyte subsets will be analyzed by flow cytometry.

    Time frame: 2 years

  14. Immunogenicity

    Incidence of anti-CD19-CAR antibodies and antiviral antibodies.

    Time frame: 2 years

  15. Viral shedding

    Peripheral blood, urine, saliva, and fecal samples will be collected at predefined time points for the assessment of viral shedding.

    Time frame: 2 years

  16. Replication-competent virus detection

    Peripheral blood, urine, saliva, and fecal samples will be collected at predefined time points for the assessment of viral shedding.

    Time frame: 2 years

  17. Viral integration site analysis

    Peripheral blood, urine, saliva, and fecal samples will be collected at predefined time points for the assessment of viral shedding.

    Time frame: 2 years

07

Study locations

No study locations are listed for this record.

08

Timeline

1 registry update since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Dec 2026; primary completion for Dec 2029, 36 months later.

Of 52 non-industry phase 1/2 interventional studies under Lymphoma, B-Cell, half reached primary completion within 64 months of starting (the median), counting those still running; a quarter within 45 and three quarters within 82. This study's planned 36 months is below that.

Counting every sponsor, half of 94 studies reached it within 71 months; a quarter within 55 and three quarters within 96.

How these figures are worked out, and which studies are left out of them.

Registered
Oct 22, 2026
First posted
Oct 29, 2026
StartEst.
Dec 15, 2026
Primary completionEst.
Dec 15, 2029
CompletionEst.
Dec 15, 2031
Last update
Oct 29, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
Registered
First appeared on the registry. No changes since
Oct 29, 2026
Show all 1 update
  1. Oct 29, 2026
    First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

09

Registry details

Key details

Study ID
NCT07905261
Lead sponsor
Beijing Kangchuanglian Biopharmaceutical Technology Research Co., Ltd
Responsible party
Sponsor
First posted
Oct 29, 2026
Start date
Dec 15, 2026 (estimated)
Primary completion
Dec 15, 2029 (estimated)
Completion
Dec 15, 2031 (estimated)
Last update
Oct 29, 2026

Study contacts

Clinical Trials Information Group officer
Contact
ctr-contact@cspc.cn
86-0311-69085587

Oversight

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

Not currently enrolling

This study is not yet recruiting, as verified in Oct 2026. You cannot join it, but the record below documents what was studied.

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Discussion

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Studies of the drug tested here: SYS6055

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