Phase 2 Lymphoma Trial, Recruiting NCT07240194 Sponsor: The First Affiliated Hospital with Nanjing Medical University Condition: Lymphoma
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Phase 2 Lymphoma Trial, Recruiting

NCT07240194
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 signed a consent form before any study-related procedures begin
  • People aged 18 or older at the time of signing consent
  • People who have been diagnosed with a specific type of blood cancer called large B-cell lymphoma (LBCL), confirmed by laboratory testing, and whose cancer cells carry a protein called CD20 — this includes several subtypes of LBCL (confirm with trial site for full list)
  • People whose lymphoma has come back after being in remission for more than 6 months, or whose lymphoma did not respond to treatment or got worse within 6 months of finishing their last treatment
  • People whose cancer has a specific gene change — either a deletion or mutation in a gene called TP53 — confirmed by specialist laboratory testing
  • People who are not suitable candidates for a stem cell transplant using their own cells (ASCT), for reasons such as being aged 70 or older, having serious organ problems, having a lower ability to carry out daily activities, choosing not to have the transplant, or having other significant health conditions as determined by the treating doctor
  • People who have at least one measurable area of disease at the start of the trial — either a lymph node measuring at least 1.5 cm, or a lesion outside the lymph nodes measuring at least 1.0 cm
  • People with a general health and activity level rated 0, 1, or 2 on a standard medical scale (confirm with trial site what this means for individual circumstances)
  • People expected to live for at least 12 weeks, as assessed by the treating doctor
  • People with blood counts at an adequate level (unless low counts are directly caused by the lymphoma affecting the bone marrow or spleen)
  • People who are willing to follow all study procedures, including contraception requirements if there is a possibility of pregnancy during the trial

Who may not be able to join:

  • People who have previously had a stem cell transplant using donor cells, or who have had an organ transplant
  • People whose lymphoma has spread to the central nervous system (brain and spinal cord) and is currently active
  • People with active autoimmune conditions that require treatment with medicines that suppress the immune system
  • People with uncontrolled infections, including active hepatitis B, hepatitis C, or HIV
  • People who have previously been treated with Glofitamab, another bispecific antibody that targets both CD20 and CD3, or a combination of a PD-1 inhibitor with a medicine called Lenalidomide
  • People who have had a serious allergic reaction to monoclonal antibody medicines or to any ingredient in the study drugs
  • People who are currently taking part in another clinical trial involving an experimental treatment
  • People who have used certain immune-suppressing medicines within the 14 days before enrolling (some steroid medicines used to treat lymphoma or manage side effects may be an exception — confirm with trial site)
  • People who are pregnant or breastfeeding
  • People who have psychological, social, or medical circumstances that the treating doctor believes could affect their ability to follow the study or could put their safety at risk

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 20 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: 86-2568302182

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 September 2025
Est. completion
30 December 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Best Complete Response Rate (BCR)

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: 20 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