RecruitingPhase 1NCT07525141

A Study of JNJ-1761981 in Participants With Solid Tumors

Phase 1 Study of Intratumoral Administration of JNJ-1761981 ER, an Extended Release Chemotherapy, in Participants With Solid Tumors


Sponsor

Johnson & Johnson Enterprise Innovation Inc.

Enrollment

66 participants

Start Date

May 18, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of Part 1 of this study is to determine a safe, tolerable, and feasible recommended total dose of intratumorally administered JNJ-1761981. The purpose of Part 2 of this study is to identify the optimal volumetric dose of JNJ-1761981 for the treatment of tumor lesions.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Cetrelimab and a drug called JNJ-1761981 for people with neoplasms. The study is currently recruiting participants at 2 locations. People eligible for this study include aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGJNJ-1761981

JNJ-1761981 will be administered intratumorally.

DRUGCetrelimab

Cetrelimab will be administered intravenously.


Locations(4)

Mayo Clinic in Florida

Jacksonville, Florida, United States

Mayo Clinic Rochester

Rochester, Minnesota, United States

Montefiore Medical Center

The Bronx, New York, United States

MD Anderson Cancer Center

Houston, Texas, United States

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NCT07525141


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