Phase 2 Lymphoma Trial, Recruiting NCT06316427 Sponsor: Beijing GoBroad Hospital Condition: Lymphoma
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Phase 2 Lymphoma Trial, Recruiting

NCT06316427
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:

  • People who have a type of blood cancer called a T-cell malignancy where the cancer cells carry a protein called CD7, and whose cancer has come back or stopped responding to treatment, having already tried all standard options (such as chemotherapy or stem cell transplant)
  • People whose cancer has been confirmed to carry the CD7 protein through specialised laboratory testing of bone marrow, spinal fluid, or tumour tissue samples
  • People aged between 1 and 70 years old, either male or female
  • People with no history of severe allergic reactions
  • People who are reasonably well and able to carry out daily activities, as measured by a standard medical scoring system (a score of 0–2 on the ECOG scale — confirm with trial site if unsure what this means)
  • People who are expected to live for at least 60 days, as assessed by the treating doctor
  • People who are able to give signed consent before any trial procedures begin; for children aged 1–7, a legal guardian must sign consent; for those aged 8–18, both the young person and a legal guardian must sign; adults aged 19–70 must be able to sign consent themselves

Who may not be able to join:

  • People with raised pressure in the brain or who are unconscious
  • People with acute heart failure or a serious irregular heartbeat
  • People with acute respiratory (breathing) failure
  • People who have another type of cancer in addition to their T-cell malignancy
  • People with a condition where blood clots form abnormally throughout the body (called diffuse intravascular coagulation)
  • People whose kidney function markers (creatinine and/or blood urea nitrogen) are more than 1.5 times higher than the normal range
  • People with blood poisoning (sepsis) or any other infection that is not under control
  • People with diabetes that is not well controlled
  • People with a serious psychological or psychiatric condition
  • People who have noticeable lesions or abnormalities in the brain shown on an MRI scan
  • People with a known tendency toward allergic reactions
  • People who have received an organ transplant
  • People who are pregnant or breastfeeding
  • People who have an active, uncontrolled infection including hepatitis B, hepatitis C, HIV, or syphilis

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 6 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

Phone: 86+18611422920

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
Sponsor
Beijing GoBroad Hospital
Registry
ClinicalTrials.gov
Start date
22 March 2024
Est. completion
1 April 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Dose-Limiting Toxicity (DLT) in phase I; Overall Response Rate (ORR) in phase II

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: 6 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