Phase 2 Lymphoma Trial, Recruiting NCT07448324 Sponsor: The First Affiliated Hospital with Nanjing Medical University Condition: Lymphoma
Back to Lymphoma

Phase 2 Lymphoma Trial, Recruiting

NCT07448324
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 sex
  • People who have been diagnosed with a specific type of lymphoma called CD20-positive marginal zone lymphoma (which includes MALT, SMZL, and NMZL subtypes), confirmed by a tissue test, with at least one measurable area of disease
  • People whose lymphoma is at an advanced stage (Stage III or IV) and has been assessed as needing treatment
  • People who have not previously received any systemic (whole-body) treatment for this lymphoma — though prior local treatments such as surgery, radiotherapy, or certain antibiotic or antiviral therapies are acceptable if the disease later came back or was not suitable for further local treatment
  • People whose general physical functioning falls within an acceptable range on a standard medical scale (ECOG score of 0–2, meaning the person is fully active to partially restricted but able to care for themselves)
  • People whose blood counts, liver function, kidney function, and other organ measures fall within the required ranges set by the trial (confirm with trial site for specific values)
  • People whose blood clotting levels are within an acceptable range
  • People whose expected survival is at least 12 months
  • People who are willing and able to provide written consent before any trial screening begins

Who may not be able to join:

  • People who currently have, or have previously had, another cancer — unless it was treated with the intent to cure and there has been no sign of it returning or spreading in the past 5 years
  • People whose lymphoma has spread to the central nervous system (brain or spinal cord), or whose lymphoma has changed into a more aggressive (high-grade) form
  • People with serious or uncontrolled heart conditions, including moderate-to-severe heart failure, unstable chest pain, a heart attack within the past 6 months, certain heart rhythm problems, a weakened heart pump (reduced ejection fraction), certain types of heart muscle disease, a history of significant abnormalities in heart electrical activity, coronary artery disease requiring medication, or blood pressure that remains poorly controlled despite multiple medications
  • People who have had active bleeding within the past 2 months, are currently using blood-thinning medications, or have any condition the trial doctor considers a significant bleeding risk
  • People who have had a blood clot in a deep vein or in the lungs within the past 6 months
  • People who have previously received an organ transplant or a bone marrow transplant from a donor
  • People who have had major surgery within the past 6 weeks, or minor surgery within the past 2 weeks (placement of a vascular access device is not counted)
  • People with an active infection requiring treatment, or with uncontrolled hepatitis B, hepatitis C, HIV/AIDS, or other serious infectious diseases
  • People with serious ongoing lung conditions such as pulmonary fibrosis, interstitial pneumonia, or radiation- or drug-related lung damage
  • People who have previously been treated with certain targeted therapies known as BTK inhibitors, BCR pathway inhibitors (such as PI3K or Syk inhibitors), or BCL-2 inhibitors
  • People who are pregnant, breastfeeding, or who are unwilling to use effective contraception if there is a possibility of pregnancy
  • People who are currently taking certain medications that strongly affect how the body processes drugs (specifically moderate or strong CYP3A inhibitors, or strong CYP3A inducers) — (confirm specific medications with trial site)
  • People who have any other condition that the trial doctor considers would make participation 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

Phone: +86 13813976136

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
1 April 2025
Est. completion
1 January 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Complete response rate (CRR)

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