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Completed Phase 1 Interventional

Study to Evaluate the Safety and Tolerability of CC-94676 in Participants With Metastatic Castration-Resistant Prostate Cancer

ClinicalTrials.gov ID: NCT04428788

Public ClinicalTrials.gov record NCT04428788. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 20, 2026, 6:21 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 1, Multi-center, Open-label, Dose Finding Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Cc-94676 in Subjects With Metastatic Castration-resistant Prostate Cancer

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to assess the safety, tolerability and preliminary efficacy of CC-94676 in men with progressive metastatic castration resistant prostate cancer.

Study identification

NCT ID
NCT04428788
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Celgene
Industry
Enrollment
131 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
Male
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 22, 2020 (Actual)
Primary completion
Oct 28, 2025 (Actual)
Completion
Oct 28, 2025 (Actual)
Last update posted
Dec 22, 2025

2020 – 2025

United States locations

U.S. sites
19
U.S. states
13
U.S. cities
17
Facility City State ZIP Site status
Local Institution - 116 Stanford California 94305-5826 —
Local Institution - 122 Washington D.C. District of Columbia 20010 —
Local Institution - 103 Sarasota Florida 34232 —
Local Institution - 121 Thomasville Georgia 31792 —
Local Institution - 108 Baltimore Maryland 21287 —
Local Institution - 104 Boston Massachusetts 02215 —
Local Institution - 117 Ann Arbor Michigan 48109 —
Local Institution - 102 Grand Rapids Michigan 49546 —
Local Institution - 112 New York New York 10029 —
Local Institution - 109 New York New York 10032 —
Local Institution - 105 New York New York 10065 —
Local Institution - 106 Durham North Carolina 27710 —
Local Institution - 120 Allentown Pennsylvania 18103 —
Local Institution - 113 Philadelphia Pennsylvania 19104 —
Local Institution - 107 Dallas Texas 75235 —
Local Institution - 119 Houston Texas 77030 —
Local Institution - 101 San Antonio Texas 78229 —
Local Institution - 115 Seattle Washington 98109 —
Local Institution - 111 Madison Wisconsin 53792 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04428788, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 22, 2025 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04428788 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →