Lymphoma Trial, Recruiting NCT06779435 Sponsor: Ruijin Hospital Condition: Lymphoma
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Lymphoma Trial, Recruiting

NCT06779435
Recruiting Not Applicable

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 not previously received any treatment for their DLBCL (diffuse large B-cell lymphoma), including chemotherapy, targeted therapy, or immunotherapy
  • People who have been confirmed by pathology (laboratory tissue testing) to have a specific type of DLBCL where two particular proteins — MYC and BCL2 — are both highly active (called "double expression"), OR people whose DLBCL does not meet that definition but who have at least one of the following: certain gene mutations including TP53 or other specific genetic changes as listed in the trial criteria, or a specific genetic finding called "MYC and BCL2 double hit" (confirm with trial site for details on which gene mutations apply)
  • People who are planned to receive, or are already receiving, a treatment plan that includes a medicine called tucidinostat (including cases where tucidinostat may be added after genetic test results become available)
  • People who are willing to sign an informed consent form agreeing to take part

Who may not be able to join:

  • People who are currently enrolled in, or planning to join, any other interventional clinical trial
  • People whose expected survival is less than 6 months
  • People where the trial investigators have identified any other reason they consider 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 15 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Phone: 13564015001

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
Not Applicable
Sponsor
Registry
ClinicalTrials.gov
Start date
1 January 2025
Est. completion
31 December 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

EFS(Event-free survival)

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: 15 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