Phase 2 Lymphoma Trial, Recruiting NCT07001540 Sponsor: Fudan University Condition: Lymphoma
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Phase 2 Lymphoma Trial, Recruiting

NCT07001540
Recruiting Phase 2

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • Adults aged 18 or older
  • People who are not suitable for a stem cell transplant using their own cells
  • People who have given written consent to participate in the study
  • People whose lymphoma has been confirmed by a lab test to be a specific type called CD79b-positive DLBCL (this includes certain related subtypes)
  • People who have received one prior course of treatment that included both an anti-CD20 antibody medicine (such as rituximab) and a chemotherapy drug from the anthracycline family, and no more than this one course of treatment
  • People whose lymphoma came back after responding to first-line treatment, or whose lymphoma did not fully respond to first-line treatment
  • People who are reasonably well and able to carry out daily activities, with a life expectancy of more than 12 weeks (confirm with trial site)
  • People who have at least one area of lymphoma that can be measured on a scan or clinical examination, meeting specific size requirements
  • People whose blood counts, liver, kidneys, lungs, and heart are all functioning at an acceptable level as determined by test results
  • People of childbearing potential who are willing to use highly effective contraception during the study and for 120 days after the last treatment dose

Who may not be able to join:

  • People who have conditions — medical, personal, family, or practical — that would make it difficult to follow the study requirements, as judged by the study doctor
  • People who have HIV infection or test positive for HIV
  • People with active or uncontrolled viral infections such as active herpes, active hepatitis B, or active hepatitis C (people who are long-term hepatitis B carriers with very low virus levels may still be considered; people with a positive hepatitis C antibody test will need further testing before a decision is made — confirm with trial site)
  • People whose lymphoma has spread to the brain or spinal cord and is not fully under control (people who had brain involvement at the original diagnosis but achieved and maintained complete remission may still be considered — confirm with trial site)
  • People who have previously been treated with the chemotherapy drugs oxaliplatin or gemcitabine
  • People who are pregnant or breastfeeding
  • People with other serious illnesses or medical conditions that would make participation unsafe

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 26 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Wenhao Zhang, M.D, Fudan University

Phone: 021-64175590

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Phase 2
Registry
ClinicalTrials.gov
Start date
8 May 2025
Est. completion
15 November 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Invetigator-assessed Objective Response Rate (ORR)

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 26 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov