Phase 2 Lymphoma Trial, Recruiting NCT06341556 Sponsor: Fudan University Condition: Lymphoma
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Phase 2 Lymphoma Trial, Recruiting

NCT06341556
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 have been diagnosed with mantle cell lymphoma (a type of blood cancer), confirmed through a tissue sample test
  • People whose mantle cell lymphoma responded to first-line treatment — either fully (complete response) or partially (partial response) — after receiving at least 4 cycles of treatment that included a type of drug called a CD20 antibody (such as rituximab-based combinations)
  • People who have previously had an autologous stem cell transplant (using their own stem cells) are still able to be considered
  • People with a general health and activity level rated at 0, 1, or 2 on a standard medical scale (meaning able to carry out daily activities, possibly with some limitations)
  • People whose blood, liver, kidney, and heart function all meet specific healthy minimum levels as measured by blood tests and a heart ultrasound (confirm exact values with trial site)
  • People who are willing and able to sign a consent form agreeing to take part

Who may not be able to join:

  • People with a known allergy to human or mouse monoclonal antibodies, or to a specific drug called Zanubrutinib or any of its ingredients
  • People who have had major surgery in the 4 weeks before joining the trial (routine diagnostic procedures are not included)
  • People with serious ongoing health conditions that are not well controlled, including severe infections, significant heart failure, poorly controlled irregular heartbeat, uncontrolled high blood pressure, unstable chest pain, active stomach ulcers, or bleeding disorders
  • People with other serious health conditions that would interfere with standard treatment
  • People with a history of another active cancer, except for certain skin cancers or early-stage cervical cancer that were treated with curative intent and have not come back within the past 3 years
  • People with known active interstitial pneumonia (a type of lung inflammation)
  • People with a known history of alcohol or drug misuse
  • People with an active hepatitis B infection (based on a virus level blood test); people with past or inactive hepatitis B may still be considered if virus levels are undetectable, provided they agree to regular monitoring and antiviral treatment as required (confirm with trial site)
  • People with active hepatitis C infection, unless a specific virus RNA test comes back negative
  • People with active HIV or syphilis infections
  • People who are pregnant or currently breastfeeding
  • People who have received a live vaccine within 4 weeks before the trial treatment begins (standard inactivated flu vaccines are generally allowed)
  • People currently taking corticosteroid medicines (such as prednisone) at a dose greater than 30mg per day for 10 or more days continuously
  • People who have needed ongoing systemic (whole-body) treatment for an active autoimmune disease within the past 2 years (some exceptions may apply, such as people who only need hormone replacement or thyroid medication — confirm with trial site)
  • People who have difficulty swallowing and cannot reliably take oral medication long-term
  • People with a mental health condition that affects their ability to follow the trial requirements or give informed consent
  • People the trial investigators determine are otherwise not suitable for the study

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 9 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: Yizhen Liu, M.D., Ph.D., Fudan University

Phone: 02164175590

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
24 May 2024
Est. completion
1 March 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

2-year progression-free survival (PFS)

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: 9 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