Phase 3 Lymphoma Trial, Recruiting NCT05018520 Sponsor: Ruijin Hospital Condition: Lymphoma
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Phase 3 Lymphoma Trial, Recruiting

NCT05018520
Recruiting Phase 3

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 specific type of lymphoma called CD20-positive Diffuse Large B-Cell Lymphoma (DLBCL), confirmed by laboratory testing using the 2016 WHO classification system
  • People whose lymphoma went into complete remission (no signs of cancer detected) after 4 cycles of a treatment called R-CHOP, as confirmed by a PET-CT scan with a specific score of 1 or 2 on the Deauville scale
  • People who have not previously received any treatment for this lymphoma
  • People with a low-risk score on a cancer severity scale called the International Prognostic Index (IPI score of 0 or 1)
  • People aged 14 to 75 years old
  • People whose tumour lesion measured less than 7.5 cm in length
  • People with a good general health and activity level, rated 0 or 1 on a standard medical scale called the ECOG scale
  • People with a life expectancy of more than 6 months
  • People who have given informed written consent to participate

Who may not be able to join:

  • People who have previously received any systemic or local cancer treatment, including chemotherapy, for any condition
  • People who have previously had an autologous stem cell transplant
  • People who have a history of another type of cancer, except for basal cell skin cancer or early-stage cervical cancer
  • People who have uncontrolled heart or blood vessel disease, blood clotting disorders, connective tissue diseases, or serious active infections
  • People whose lymphoma started in the skin or the central nervous system (brain and spinal cord)
  • People whose heart's pumping function (left ventricular ejection fraction) is at or below 50%, as measured by a heart scan
  • People with other ongoing, uncontrolled medical conditions that the research team believes would affect their health or participation
  • People whose blood test results during the screening period fall outside acceptable ranges — specifically, those with low white blood cell counts, low platelet counts, low haemoglobin (anaemia), or abnormal liver or kidney function — unless those abnormalities are directly caused by the lymphoma (confirm with trial site)
  • People with a psychiatric condition or any other situation that may make it difficult for them to follow the trial's requirements
  • Women who are pregnant or breastfeeding
  • People with certain results on Hepatitis B blood tests may not be eligible unless further testing (HBV-DNA testing) shows the virus is not active; specific rules apply depending on which Hepatitis B markers are detected (confirm with trial site for full details)
  • People who are living with HIV
  • People who have a TP53 gene mutation in their lymphoma, or people who have not had their lymphoma tested for key genetic mutations (DLBCL hot spot gene screening)

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 3: approximately ~65% 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: +862164370045

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 3
Sponsor
Registry
ClinicalTrials.gov
Start date
17 September 2021
Est. completion
30 June 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Progression of disease within 24 months

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