Fact CheckerSign in

NCT04428788CompletedPhase 1

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

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

Source: ClinicalTrials.gov · Last updated 22 Dec 2025

Brief summary (registry, in English)

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.

Status (registry)
Completed
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
131 (actual)
First submitted
29 May 2020
Start date
22 Jun 2020
Primary completion date
28 Oct 2025
Lead sponsor
Celgene
NCT number
NCT04428788

What you commit to

  • Study type: Interventional · Phase 1
  • Participants enrolled: 131
  • From 22 Jun 2020 to the primary completion date, 28 Oct 2025
  • 19 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior treatment with an androgen receptor (AR) degrader
  • Clinically significant venous thromboembolism within 3 months prior to the first dose of IP

Other illness

  • Concurrent malignancy (present during screening) requiring treatment or history of prior malignancy active within 1 year prior to the first dose of IP

Lab values

  • Any significant medical condition, such as uncontrolled infection, laboratory abnormality, or psychiatric illness
    • Other protocol-defined inclusion/exclusion criteria apply

Who the study is looking for

  • Must have histologically or cytologically confirmed adenocarcinoma of the prostate
  • Progressed on androgen deprivation therapy (ADT) and at least one prior secondary hormonal therapy approved for castration-resistant prostate cancer (CRPC)
  • Eastern Cooperative Oncology Group (ECOG) performance status (PS) 0 or 1

Age in the registry: 18 years to - · Sex: Male · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (19)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Local Institution - 120
Coordinator of this site? Confirm its status
AllentownUnited StatesUnknown status
Local Institution - 117
Coordinator of this site? Confirm its status
Ann ArborUnited StatesUnknown status
Local Institution - 108
Coordinator of this site? Confirm its status
BaltimoreUnited StatesUnknown status
Local Institution - 104
Coordinator of this site? Confirm its status
BostonUnited StatesUnknown status
Local Institution - 107
Coordinator of this site? Confirm its status
DallasUnited StatesUnknown status
Local Institution - 106
Coordinator of this site? Confirm its status
DurhamUnited StatesUnknown status
Local Institution - 102
Coordinator of this site? Confirm its status
Grand RapidsUnited StatesUnknown status
Local Institution - 119
Coordinator of this site? Confirm its status
HoustonUnited StatesUnknown status
Local Institution - 111
Coordinator of this site? Confirm its status
MadisonUnited StatesUnknown status
Local Institution - 112
Coordinator of this site? Confirm its status
New YorkUnited StatesUnknown status
Local Institution - 105
Coordinator of this site? Confirm its status
New YorkUnited StatesUnknown status
Local Institution - 109
Coordinator of this site? Confirm its status
New YorkUnited StatesUnknown status
Local Institution - 113
Coordinator of this site? Confirm its status
PhiladelphiaUnited StatesUnknown status
Local Institution - 101
Coordinator of this site? Confirm its status
San AntonioUnited StatesUnknown status
Local Institution - 103
Coordinator of this site? Confirm its status
SarasotaUnited StatesUnknown status
Local Institution - 115
Coordinator of this site? Confirm its status
SeattleUnited StatesUnknown status
Local Institution - 116
Coordinator of this site? Confirm its status
StanfordUnited StatesUnknown status
Local Institution - 121
Coordinator of this site? Confirm its status
ThomasvilleUnited StatesUnknown status
Local Institution - 122
Coordinator of this site? Confirm its status
Washington D.C.United StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.