Phase 2 Lymphoma Trial, Recruiting NCT07507318 Sponsor: Rong Tao Condition: Lymphoma
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Phase 2 Lymphoma Trial, Recruiting

NCT07507318
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 a specific type of blood cancer called diffuse large B-cell lymphoma, confirmed by laboratory testing of tissue samples, where the cancer cells test positive for a protein called CD20.
  • People whose lymphoma has been confirmed by a pathologist to be a "double-expressor" type, meaning the cancer cells show high levels of two specific proteins (MYC at 40% or above, and BCL2 at 50% or above).
  • People whose cancer showed a complete response (no detectable cancer) after their first course of treatment.
  • People aged 18 to 80 years.
  • People whose general physical health and ability to carry out daily activities falls within a certain range, as assessed using a standard medical scale (confirm with trial site).
  • People with no history of any other cancer, either in the past or currently.
  • People whose lymphoma is rated above a score of 1 on a standard risk-assessment tool called the International Prognostic Index (confirm with trial site).
  • People who test positive for a specific marker in the blood called ctDNA MRD at the time of enrolling in the trial, which indicates a small amount of cancer-related material may still be present.
  • People expected to live for at least 6 months, based on the treating doctor's assessment.
  • People who provide written consent before any trial procedures begin.

Who may not be able to join:

  • People whose cancer did not achieve a complete response after their first course of treatment.
  • People who have previously had an organ transplant.
  • People with uncontrolled blood clotting problems or active bleeding.
  • People with uncontrolled heart or blood vessel disease, including reduced heart pumping function (below 50%), certain connective tissue conditions, or serious active infections.
  • People who had major surgery within 6 weeks before joining the trial.
  • People whose routine blood test results — for reasons unrelated to their lymphoma — fall outside acceptable ranges, including low white blood cell counts, low platelet counts, or abnormal liver or kidney function levels (confirm with trial site for specific thresholds).
  • People with active hepatitis B infection that does not meet specific virus level requirements set by the trial (people who test positive for certain hepatitis B markers will need additional testing to determine whether they meet the trial's requirements).
  • People with HIV infection.
  • People currently receiving any cancer treatment for lymphoma or another cancer.
  • People with drug or alcohol dependence that may affect how trial results are assessed.
  • People with a psychiatric illness or any condition that would make it difficult to follow the trial's requirements.
  • People who need to take certain medications that strongly affect how the body processes drugs (called CYP3A inhibitors or inducers), or who have taken these medications within 7 days — or within a set number of half-lives — before the first trial dose (confirm with trial site).
  • People who cannot swallow capsules, or who have significant digestive system conditions that may affect how the body absorbs medication, such as malabsorption conditions, previous weight-loss surgery, inflammatory bowel disease, or bowel blockage.
  • People with any other serious uncontrolled medical condition that the trial doctor believes could affect safety, drug absorption, or place the person at unacceptable risk.

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: Rong Tao, MD & PhD, Fudan University

Phone: 008621-64175590

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
Sponsor
Rong Tao
Registry
ClinicalTrials.gov
Start date
16 June 2026
Est. completion
30 June 2029

Where this trial is recruiting

🇨🇳 China

Primary endpoints

ctDNA MRD Negativity Rate; 2-Year Progression-Free Survival 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: 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