Phase 2 Lymphoma Trial, Recruiting NCT07372365 Sponsor: The First Affiliated Hospital of Soochow University Condition: Lymphoma
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Phase 2 Lymphoma Trial, Recruiting

NCT07372365
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 type of lymphoma called CD20-positive marginal zone lymphoma (MZL), confirmed by a tissue test, and who have not yet received any systemic (whole-body) treatment for it.
  • People whose MZL has come back or gotten worse after a local treatment — such as surgery, radiation therapy, or treatment for a bacterial or viral infection linked to the lymphoma — or whose lymphoma is not suitable for local treatment.
  • People aged 18 or older.
  • People whose doctor has determined that treatment is needed, or who are willing to receive treatment.
  • People who are reasonably active and able to care for themselves, as measured by a standard medical scoring tool called the ECOG scale (score of 0, 1, or 2).
  • People whose heart, kidneys, liver, and blood cell counts meet certain minimum levels of healthy function, as assessed by the trial site through blood and heart tests (confirm with trial site for specific thresholds).
  • Women who could become pregnant must have a negative pregnancy test before joining, and both men and women must agree to use effective contraception during treatment and for 2 years after.
  • People with a life expectancy of more than 3 months.
  • People who are willing and able to provide written consent to participate.

Who may not be able to join:

  • People who have had major surgery or a serious physical injury within the 2 weeks before enrolment, or who have not yet fully recovered from its effects.
  • People who currently have, or have had within the past 3 years, another type of cancer — unless it has been fully cured (some minor skin cancers and certain other early-stage cancers may be exceptions; confirm with trial site).
  • People who have had a stroke or bleeding in the brain within the past 3 months.
  • People who need to take warfarin or a similar blood-thinning medication.
  • People with serious heart conditions — such as severe heart failure, a heart attack in the past 6 months, or unstable heart rhythms — or serious lung conditions, such as severe breathing difficulties or a history of significant airway spasms.
  • People who are living with HIV, or who have hepatitis B or hepatitis C that is currently active and not under control.
  • People who have an active infection that cannot be controlled.
  • People who are currently pregnant or breastfeeding.
  • People with any life-threatening illness or serious organ problem that the trial doctor believes would put them at unacceptable risk.
  • People who have a condition that may interfere with how the trial drug (orelabrutinib) is absorbed or processed by the body.
  • People whose lymphoma has spread to the brain or spinal cord, or whose lymphoma has transformed into a more aggressive type.
  • People with any other condition that the trial doctor believes could affect safe participation, put the person at significant risk, or make it difficult to interpret the trial results.

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 23 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.

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Trial details

Status
Recruiting
Phase
Phase 2
Sponsor
The First Affiliated Hospital of Soochow University
Registry
ClinicalTrials.gov
Start date
24 October 2025
Est. completion
1 April 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Complete response (CR) rate after 6 treatment cycles

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: 23 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