Phase 2 Lymphoma Trial, Recruiting NCT07302347 Sponsor: Merck Sharp & Dohme LLC Condition: Lymphoma
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Phase 2 Lymphoma Trial, Recruiting

NCT07302347
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:

Arm 1 (various cancer types):

  • People with a confirmed diagnosis of classical Hodgkin lymphoma or primary mediastinal large B-cell lymphoma that has come back or stopped responding to treatment, with disease that can be measured on scans
  • People with skin melanoma (Stage IIB, IIC, III, or IV) that has been completely removed by surgery, with no prior drug-based treatments for melanoma, and where any suspicious areas have been tested and confirmed cancer-free
  • People with locally advanced (cannot be surgically removed) or metastatic (spread to other parts of the body) melanoma, including a type called acral melanoma, that cannot be treated with local therapies, with disease measurable on scans
  • People with advanced or metastatic solid tumour cancers that have a specific genetic feature called MSI-H or dMMR, where standard treatments have failed, do not exist, or are considered unsuitable by the patient and their doctor, with disease measurable on scans
  • People with advanced or metastatic solid tumour cancers that have a high number of genetic mutations (called TMB-H), where standard treatments have failed, do not exist, or are considered unsuitable, with disease measurable on scans
  • People with a rare skin cancer called Merkel cell carcinoma (MCC) that has returned after surgery and/or radiation, cannot be treated locally, or has spread to other parts of the body, with disease measurable on scans
  • People in Arm 1 must have a life expectancy of more than 3 months

Arm 2 (Merkel cell carcinoma only):

  • People with advanced or metastatic Merkel cell carcinoma who have not yet received any treatment for their advanced or metastatic disease
  • People in Arm 2 must have a life expectancy of more than 6 months

Who may not be able to join:

  • People who have another cancer that is currently growing or has recently needed active treatment
  • People with active cancer spread to the brain or the membranes surrounding the brain or spinal cord
  • People with an autoimmune disease (where the immune system attacks the body) that has required medication to treat it within the past 2 years
  • People with a history of lung inflammation (not caused by infection) that required steroid treatment, or who currently have this condition
  • People with an active infection that requires medication to treat it
  • People with a known history of HIV infection
  • People with a known history of Hepatitis B, or an active Hepatitis C infection
  • People who have ever had a solid organ transplant (such as a kidney or liver), or who received a bone marrow or stem cell transplant from a donor within the last 5 years
  • People who have not fully recovered from a major surgery, or who have ongoing complications from a surgery

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 13 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
23 June 2026
Est. completion
30 March 2029

Where this trial is recruiting

🇯🇵 Japan

Primary endpoints

Arm 1: Number of Participants Who Experience an Adverse Event (AE); Arm 1: Number of Participants Who Discontinue Study Treatment Due To an AE; Arm 1: Area Under the Concentration-Time Curve (AUC) of Pembrolizumab; Arm 1: Maximum Concentration (Cmax) of Pembrolizumab; Arm 1: Minimum Plasma Concentration (Cmin) of Pembrolizumab; Arm 2: Objective Response Rate (ORR) per Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST 1.1) by Blinded Independent Central Review (BICR)

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: 13 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