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RECRUITING
NCT07525141
PHASE1

A Study of JNJ-1761981 in Participants With Solid Tumors

Sponsor: Johnson & Johnson Enterprise Innovation Inc.

View on ClinicalTrials.gov

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.

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

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

66

Start Date

2026-05-18

Completion Date

2029-01-31

Last Updated

2026-05-14

Healthy Volunteers

No

Conditions

Interventions

DRUG

JNJ-1761981

JNJ-1761981 will be administered intratumorally.

DRUG

Cetrelimab

Cetrelimab will be administered intravenously.

Locations (2)

Montefiore Medical Center

The Bronx, New York, United States

MD Anderson Cancer Center

Houston, Texas, United States