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Clinical Trials/EUCTR2017-001626-17-DE
EUCTR2017-001626-17-DE
Active, not recruiting
Phase 1

A Phase 2 Study of Nivolumab in Combination with Either Rucaparib, Docetaxel, or Enzalutamide in Men with Castration-resistant Metastatic Prostate Cancer - CheckMate 9KD: CHECKpoint pathway and nivoluMAb clinical Trial Evaluation 9KD

Bristol-Myers Squibb International Corporation0 sites330 target enrollmentNovember 15, 2017

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Not specified
Sponsor
Bristol-Myers Squibb International Corporation
Enrollment
330
Status
Active, not recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
November 15, 2017
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional clinical trial of medicinal product
Sex
Male

Investigators

Eligibility Criteria

Inclusion Criteria

  • \- Histologic confirmation of adenocarcinoma of the prostate
  • \- Evidence of stage IV disease
  • \- Ongoing androgen deprivation therapy (ADT) with a gonadotropin\-releasing hormone (GnRH) analogue or bilateral orchiectomy
  • \- Mandatory plasma and, fresh or archival tumor tissue must be submitted
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1\.2 Adults (18\-64 years) yes
  • F.1\.2\.1 Number of subjects for this age range 150
  • F.1\.3 Elderly (\>\=65 years) yes
  • F.1\.3\.1 Number of subjects for this age range 150

Exclusion Criteria

  • \- Prior malignancy active within the previous 3 years except for locally curable cancers that have been apparently cured, such as basal or squamous cell skin cancer, superficial bladder cancer, or carcinoma in situ of the breast
  • \- Participants with active brain metastases
  • \- Participants must have recovered from the effects of major surgery requiring general anesthesia or significant traumatic injury at least 14 days before treatment arm assignment

Outcomes

Primary Outcomes

Not specified

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