Phase 2 Lymphoma Trial, Recruiting NCT07554898 Sponsor: Zhejiang Cancer Hospital Condition: Lymphoma
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Phase 2 Lymphoma Trial, Recruiting

NCT07554898
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 of any gender
  • People who have been confirmed by tissue testing to have MALT lymphoma (a type of slow-growing lymphoma that starts in organs outside lymph nodes), with at least one affected area larger than 1.0 cm that can be measured, located outside the spleen
  • People who have not yet received any systemic anti-cancer treatment (such as chemotherapy, targeted therapy, or rituximab) since their diagnosis — with a note that people whose lymphoma progressed or came back after local treatments (such as surgery, antibiotic treatment for stomach bacteria, or hepatitis C treatment) may still be eligible; for stomach MALT lymphoma specifically, the stomach bacteria called Helicobacter pylori must either be absent or have not responded to standard treatment (confirm with trial site)
  • People who are generally well enough to carry out normal daily activities with little or no limitation (based on a standard medical scale scored 0 or 1)
  • People whose doctor has determined that treatment is needed, based on symptoms, low blood counts, risk of organ damage, a large disease burden, or ongoing disease progression
  • People whose blood counts and organ function meet specific minimum levels — including adequate levels of white blood cells, platelets, and red blood cells, as well as acceptable liver, kidney, and pancreas function, and normal blood clotting levels (confirm specific values with trial site)
  • People with an expected survival of at least 3 months
  • People who are willing and able to give written consent before any screening begins

Who may not be able to join:

  • People who currently have, or have previously had, another type of cancer, unless it was fully treated and has completely resolved
  • People whose lymphoma has spread to the brain or spinal cord, or whose lymphoma has changed into a more aggressive (high-grade) form
  • People who have had treatment for another cancer and are still experiencing significant side effects from that treatment (above a mild level), not including hair loss
  • People with serious or uncontrolled heart conditions, including moderate-to-severe heart failure, unstable chest pain, a heart attack in the past 6 months, heart rhythm problems requiring treatment, a weakened heart pump function, certain structural heart muscle diseases, a history of a specific abnormal heart electrical measurement (QTc interval), heart artery disease requiring medication, or high blood pressure that cannot be adequately controlled even with multiple medications
  • People who have had significant active bleeding in the 2 months before screening, are currently taking blood-thinning medications, or are assessed by their doctor as having a clear risk of bleeding
  • People with high levels of protein in their urine, above certain measured thresholds (confirm with trial site)
  • People who have had a blood clot in a deep vein or in the lungs within the past 6 months
  • People who have had an organ transplant or a bone marrow/stem cell transplant from another person
  • People who have had major surgery (performed under general anaesthetic) within 6 weeks before screening, or minor surgery within 2 weeks before screening — though placement of a vascular access device and diagnostic camera examinations are not counted as exclusions
  • People living with HIV/AIDS or other serious infectious diseases
  • People with severe lung function problems caused by conditions such as pulmonary fibrosis, interstitial lung disease, dust-related lung disease, or lung damage from radiation or medication
  • People who have previously been treated with certain targeted drugs that affect specific cell signalling pathways involved in lymphoma (BTK inhibitors, BCR pathway inhibitors such as PI3K or Syk inhibitors, or BCL-2 inhibitors)
  • People with a history of drug or alcohol misuse
  • People who are pregnant or breastfeeding, or people who could become pregnant and are unwilling to use contraception during the trial
  • People who, in their doctor's judgement, have any other condition that makes participation in this trial 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 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: Yamin Tan, phD, Zhejiang Cancer Hospital

Phone: 8657188122153

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
Zhejiang Cancer Hospital
Registry
ClinicalTrials.gov
Start date
16 April 2026
Est. completion
1 February 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Complete Remission Rate (CRR); Incidence of Adverse Events

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