A Study of JNJ-63898081 in Participants With Advanced Stage Solid Tumours

Official Title

A Phase 1, First-in-Human, Dose Escalation Study of JNJ-63898081, in Subjects With Advanced Stage Solid Tumours


The main purpose of this study are to determine the recommended Phase 2 dose (RP2D) regimen and the maximum tolerated dose, and to determine the safety of JNJ-63898081.

Trial Description

Primary Outcome:

  • Part 1 and Part 2: Number of Participants with Adverse Events (AEs) as a Measure of Safety and Tolerability
  • Part 1: Number of Participants with Dose-Limiting Toxicity (DLT)
  • Part 1: Severity of Adverse Events as Assessed by National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE)
Secondary Outcome:
  • Part 1 and Part 2: Serum Concentrations of JNJ-63898081
  • Part 1 and 2: Systemic Cytokine Concentrations
  • Part 1 and 2: Number of Participants with JNJ-63898081 Antibodies
  • Serum Prostate Specific Antigen (PSA) Concentration
  • Objective Response Rate (ORR)
  • Duration of Response

View this trial on ClinicalTrials.gov

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Canadian Cancer Society

These resources are provided in partnership with the Canadian Cancer Society