Phase 1 Lymphoma Trial, Recruiting NCT06313957 Sponsor: Peking University Cancer Hospital & Institute Condition: Lymphoma
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Phase 1 Lymphoma Trial, Recruiting

NCT06313957
Recruiting Phase 1

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:

  • People who are willing to take part in clinical research voluntarily
  • People aged 18 or older
  • People whose general physical condition and ability to carry out daily activities meets a certain standard (known as an ECOG score of 0–1, meaning fully active or able to carry out light activity — confirm with trial site)
  • People who have been diagnosed through a tissue sample (biopsy) with one of the following blood cancers: large B-cell lymphoma, follicular lymphoma, mantle cell lymphoma, or a slow-growing lymphoma that has changed into a more aggressive type — and whose cancer tests positive for a protein called CD20
  • People who have at least one tumour that can be measured on a scan, based on specific 2014 assessment guidelines
  • People whose doctors expect them to live for at least 3 more months
  • People whose blood test results during the screening period fall within the required ranges
  • People who are using effective contraception

Who may not be able to join:

  • People who have recently received cancer treatments and have not waited long enough since their last treatment (confirm with trial site for required waiting periods)
  • People who have previously received a type of treatment where another person's immune cells were modified and given to them (such as CAR-T cell therapy), unless testing shows no trace of those cells or genetic material remains in the body
  • People who have previously received a bone marrow or stem cell transplant from another person
  • People who have previously received any form of gene therapy
  • People whose blood tests show the presence of certain antibodies that could cause a reaction against donor cells (called donor specific antibodies, or DSA)
  • People with serious pre-existing health conditions
  • People who test positive for active Hepatitis B, Hepatitis C, or HIV
  • People with any other serious medical condition that, in the treating doctor's judgement, would make participation unsuitable

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 7 July 2026
Phase 1: approximately ~10% 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

Phone: 13683398726

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 1
Sponsor
Peking University Cancer Hospital & Institute
Registry
ClinicalTrials.gov
Start date
14 March 2024
Est. completion
1 September 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Dose-limiting toxicity (DLT) rate; Incidence, severity, and type of treatment-emergent adverse events (TEAEs); Recommended Phase 2 Dose (RP2D) regimen finding; Pharmacokinetics in peripheral blood; Pharmacokinetics in bone marrow

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: 7 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