Phase 2 Lymphoma Trial, Recruiting NCT04922567 Sponsor: Second Affiliated Hospital, School of Medicine, Zhejiang University Condition: Lymphoma
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Phase 2 Lymphoma Trial, Recruiting

NCT04922567
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 been diagnosed with certain types of peripheral T-cell lymphoma (PTCL) confirmed by a tissue sample, including subtypes such as PTCL not otherwise specified, angioimmunoblastic T-cell lymphoma, anaplastic large cell lymphoma, enteropathy-associated T-cell lymphoma, monomorphic epitheliotropic intestinal T-cell lymphoma, nodal peripheral T-cell lymphoma with T-follicular helper phenotype, and follicular T-cell lymphoma.
  • People aged between 18 and 80 years old.
  • People who have not yet received any anti-cancer treatment for their lymphoma.
  • People with a general health status rated as able to carry out normal daily activities or light work, or who are up and about more than half the day (confirm with trial site regarding the specific fitness scale used).
  • People whose heart, liver, lung, and kidney function are within acceptable ranges, based on blood test results.
  • People with normal blood cell counts, including adequate levels of white blood cells, red blood cells, and platelets.
  • People who do not have any other serious illnesses that would conflict with the treatment plan.
  • People who do not have any other cancer diagnoses.
  • Women of childbearing age who have a negative pregnancy test at the time of enrolment.
  • People with an estimated life expectancy of at least 3 months and who are able to follow the study requirements.
  • People who are willing to participate voluntarily and have signed a written informed consent form.

Who may not be able to join:

  • People whose PTCL subtype is one of the following: extranodal natural killer/T-cell lymphoma, T-prolymphocytic leukemia, T large granular lymphocytic leukemia, chronic lymphoproliferative disorder of NK cells, aggressive NK-cell leukemia, adult T-cell leukemia/lymphoma, hepatosplenic T-cell lymphoma, subcutaneous panniculitis-like T-cell lymphoma, cutaneous T-cell lymphoma, or breast implant-associated anaplastic large-cell lymphoma.
  • People whose lymphoma has transformed from another type of lymphoma.
  • People who have had, or currently have, any other cancer, or whose lymphoma developed as a result of chemotherapy or radiotherapy for another cancer.
  • People who have already started lymphoma treatment (other than a specific pre-treatment allowed under this study).
  • People whose lymphoma affects the brain or spinal cord, or the membranes surrounding them.
  • People being considered for a stem cell transplant.
  • People with a known allergy to any of the medications used in the trial.
  • People whose blood cell counts fall below the required levels.
  • People with known liver or kidney function that does not meet the required blood test thresholds.
  • People with serious heart conditions, including severe heart failure, dilated cardiomyopathy, certain abnormal heart rhythm findings, or a heart attack within the past 6 months.
  • People with serious uncontrolled infections currently requiring treatment, or with severely impaired organ function.
  • People who have tested positive for HIV, hepatitis B surface antigen, or hepatitis C antibodies.
  • People who are pregnant or breastfeeding.
  • People who have participated in another clinical trial within the past 3 months.
  • People whom the trial researchers determine should not participate, for any reason.

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 2 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.

GP referral letter

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Trial details

Status
Recruiting
Phase
Phase 2
Registry
ClinicalTrials.gov
Start date
1 April 2021
Est. completion
31 December 2023

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Objective Response rate

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: 2 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