🔎 Trials Near Me

Home › Prostate Cancer › NCT06095089

A Study of JNJ-87189401 Combined With JNJ-78278343 for Advanced Prostate Cancer

RecruitingPhase 1

A Phase 1 Study of JNJ-87189401 (PSMA-CD28 Bispecific Antibody) Combined With JNJ-78278343 (KLK2-CD3 Bispecific Antibody) for Advanced Prostate Cancer

Who can join

Ages 18 and older · Men

Full eligibility criteria
Inclusion Criteria:

* Histologically confirmed adenocarcinoma of the prostate. Adenocarcinoma with small cell or neuroendocrine (NE) features is permitted. However, small cell carcinoma, carcinoid tumor, mixed NE carcinoma, or large cell NE carcinoma is disallowed
* Measurable or evaluable disease per PCWG3 criteria
* Part 1, Parts 2A, 2B, 3 and 4: Prior orchiectomy or medical castration; participants who have not undergone orchiectomy, must be receiving ongoing androgen deprivation therapy with a gonadotropin releasing hormone (GnRH) analog (agonist or antagonist), prior to the first dose of study drug and must continue this therapy throughout the treatment phase
* Have an Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1

Exclusion Criteria:

* History of an autoimmune disease within the 12 months prior to signing consent
* Any of the following within 6 months prior to signature of informed consent: a. myocardial infarction, b. severe or unstable angina, c. clinically significant ventricular arrhythmias, d. congestive heart failure (New York Heart Association \[NYHA\] class II to IV), e. transient ischemic attack, and f. Cerebrovascular accident

About the study

The purpose of Parts 1, 2A, and 2B of the study is to determine the recommended regimen for Phase 2 (RP2Rs) of combination of JNJ-87189401 with JNJ-78278343 and the purpose of Part 2C of this study is to determine how safe the RP2R(s) of the combination of JNJ-87189401 and JNJ-78278343 is, with or without apalutamide. Part 3 of this study evaluates the safety of the triplet combination of JNJ-87189401 and JNJ-78278343 with standard of care (SOC) lutetium Lu-177 vipivotide tetraxetan. Part 4 of this study further evaluates the safety of the triplet combination of JNJ-87189401 and JNJ-78278343 with JNJ-101556143 in participants with advanced prostate cancer.

What is being tested

Sponsor: Janssen Research & Development, LLC · Participants: 355 · Started: Nov 1, 2023

Contact the study team

Official record on ClinicalTrials.gov — NCT06095089

Locations in the U.S.

ColoradoUniversity of Colorado Anschutz Medical Campus, Aurora
GeorgiaEmory University Winship Cancer Institute, Atlanta
MinnesotaUniversity Of Minnesota, Minneapolis
New JerseySTART New Jersey, East Brunswick
New YorkHerbert Irving Comprehensive Cancer Center Columbia University Medical Center, New York
North CarolinaAtrium Health Levine Cancer Institute, Charlotte
OregonOregon Health And Science University, Portland
PennsylvaniaSidney Kimmel Cancer Center - Jefferson Health, Philadelphia
TennesseeTennessee Oncology, Nashville
TexasMD Anderson Cancer Center, Houston
South Texas Accelerated Research Therapeutics, LLC (START), San Antonio
WashingtonSwedish Medical Center, Seattle

Conditions

From ClinicalTrials.gov, data retrieved Sep 29, 2026. Each study sets its own eligibility; the study team decides who can join.