Phase 2 Lymphoma Trial, Recruiting NCT07519772 Sponsor: Merck Sharp & Dohme LLC Condition: Lymphoma
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Phase 2 Lymphoma Trial, Recruiting

NCT07519772
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 whose lymphoma has come back after treatment, or whose disease did not respond well enough to at least 2 previous treatment plans.
  • People who have been confirmed through a tissue test (biopsy) to have either follicular lymphoma (FL) or diffuse large B-cell lymphoma (DLBCL).
  • For people with DLBCL only: the disease has continued to grow after a stem cell transplant, or the treating doctor has determined they are not suitable for a transplant or a specialised cell therapy called CAR-T therapy.
  • People who are able to provide a tumour tissue sample, either from a previously stored sample or a newly collected one (if done as part of standard care).
  • People whose tumour tissue, tested after a previous treatment that targeted a protein called CD19, still shows signs of that protein — this applies only if their disease progressed after such a treatment.
  • People living with HIV whose infection is well-managed with medication.
  • People who have hepatitis B, provided the virus is undetectable in their blood and they are receiving and will continue to receive antiviral treatment.
  • People who have had hepatitis C, provided the virus is no longer detectable in their blood following antiviral treatment.
  • People whose disease can be measured on a scan, according to a standard measurement system called the Lugano Response Criteria.

Who may not be able to join:

  • People who have previously received a solid organ transplant (such as a kidney, liver, or heart).
  • People who have had or currently have significant diseases affecting the brain or spinal cord.
  • People with a history of serious heart or stroke-related conditions.
  • People who have had an allogeneic stem cell transplant (a transplant using a donor's cells) and experienced a serious immune reaction called acute graft-versus-host disease (GVHD), or who currently show signs of ongoing GVHD, or who still need medication to suppress their immune system because of GVHD.
  • People living with HIV who have also had a condition called Kaposi's sarcoma or Multicentric Castleman's Disease.
  • People who have received a live vaccine within 30 days before joining the trial.
  • People who have received CAR-T therapy within 3 months before the first dose of the trial treatment.
  • People who have another cancer that is still growing or required active treatment within the past 2 years.
  • People whose lymphoma has spread to or is active in the brain or spinal cord.
  • People who have an autoimmune disease (where the immune system attacks the body) that required treatment with medication in the past 2 years.
  • People who currently have an active infection that requires medication.
  • People with a history of severe bleeding disorders.
  • People who have not yet recovered from major surgery, or who have ongoing complications from surgery.
  • People diagnosed with a specific type of lymphoma called primary mediastinal B-cell lymphoma.

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 26 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

Principal Investigator: Medical Director, Merck Sharp & Dohme LLC

Phone: 1-888-577-8839

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
3 May 2026
Est. completion
1 July 2030

Where this trial is recruiting

🇦🇷 Argentina 🇨🇳 China 🇮🇱 Israel 🇮🇹 Italy 🇵🇱 Poland 🇪🇸 Spain Turkey (Türkiye) 🇬🇧 United Kingdom 🇺🇸 United States

Primary endpoints

Number of Participants Who Experience an Adverse Event (AE); Number of Participants Who Discontinue Study Treatment Due to an AE; Arms 2 and 3: Number of Participants Who Experience Dose Limiting Toxicity (DLT); Arms 1 and 4: Objective Response Rate (ORR) per Lugano Response Criteria as assessed by Blinded Independent Central review (BICR); Arm 2: ORR per Lugano Response Criteria as assessed by Investigator

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: 26 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