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An Investigational Immunotherapy Study of Nivolumab in Combination With Rucaparib, Docetaxel, or Enzalutamide in Metastatic Castration-resistant Prostate Cancer

Registration Number
NCT03338790
Lead Sponsor
Bristol-Myers Squibb
Brief Summary

The purpose of this study is to assess safety and efficacy of nivolumab in combination with rucaparib, docetaxel, or enzalutamide in participants with castration-resistant prostate cancer that has spread.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Male
Target Recruitment
292
Inclusion Criteria
  • Histologic confirmation of adenocarcinoma of the prostate
  • Evidence of stage IV disease on previous bone, CT, and/or MRI scan
  • 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
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

Other protocol defined inclusion/exclusion criteria could apply

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
nivolumab + docetaxel + prednisonenivolumabSpecified dose on specified days
nivolumab + rucaparibnivolumabSpecified dose on specified days
nivolumab + rucaparibrucaparibSpecified dose on specified days
nivolumab + docetaxel + prednisonedocetaxelSpecified dose on specified days
nivolumab + docetaxel + prednisoneprednisoneSpecified dose on specified days
nivolumab + enzalutamideenzalutamideSpecified dose on specified days
nivolumab + enzalutamidenivolumabSpecified dose on specified days
Primary Outcome Measures
NameTimeMethod
Objective Response Rate Per Prostate Cancer Clinical Trials Working Group 3 (ORR-PCWG3)Up to approximately 36 months

Objective response rate per prostate cancer clinical trials working group 3 (ORR-PCWG3) for target lesions and assessed by MRI is the percentage of participants who have a confirmed complete or partial best overall response (BOR) per PCWG3 among treated participants who have measurable disease

Prostate-Specific Antigen Response Rate (RR-PSA)Up to approximately 36 months

Prostate-specific antigen response rate (RR-PSA) is the percentage of treated participants with a 50% or greater decrease in PSA from baseline to the lowest post-baseline PSA result

Secondary Outcome Measures
NameTimeMethod
Duration of Response Per Prostate Cancer Clinical Trials Working Group 3 (DOR-PCWG3)Up to approximately 36 months

Duration of response per prostate cancer clinical trials working group 3 (DOR-PCWG3) is the time between the date of first response (complete response/partial response per PCWG3) to the date of first documented radiographic progression per PCWG3 or death due to any cause

Overall Survival (OS)Up to approximately 36 months

Overall Survival (OS) is the time between treatment initiation and the date of death from any cause. For participants who are alive, their survival time will be censored at the last date that they were known to be alive. OS will be censored for participants at the date of treatment initiation if they had no follow-up

Radiographic Progression-Free Survival (rPFS)Up to approximately 36 months

Radiographic progress-free survival (rPFS) is the time between treatment initiation and the first date of documented progression or death due to any cause, whichever occurs first assessed by the investigator per PCWG3

Number of Participants With Adverse Events (AEs)From first dose to up to 30 days post last dose (Up to 34 months)

Number of Participants with any grade adverse events (AEs), serious adverse events (SAEs), AEs leading to discontinuation, and immune-mediated AEs using the Common Toxicity Criteria Grade for Adverse Events (CTCAE V4)

Time to Response Per Prostate Cancer Clinical Trials Working Group 3 (TTR-PCWG3)Up to approximately 36 months

Time to response per prostate cancer clinical trials working group 3 (TTR-PCWG3) is the time from treatment initiation to the date of the first documented complete response (CR) or partial response (PR) per PCWG3

Prostate-Specific Antigen Time to Progression (TTP-PSA)Up to approximately 36 months

Prostate-specific antigen time to progression (TTP-PSA) is the time between treatment initiation to the date of PSA progression per prostate cancer clinical trails working group 3

Number of Participants With Laboratory Abnormalities in Specific Liver TestsFrom first dose to up to 30 days post last dose (up to 34 months)

Number of participants with laboratory abnormalities in specific liver tests based on SI conventional units to assess the overall safety and tolerability of BMS-986213 in combination with chemotherapy vs. Nivolumab in combination with chemotherapy. The number of participants with the following laboratory abnormalities from on-treatment evaluations will be summarized:

* ALT or AST \> 3 x ULN, \> 5 x ULN, \> 10 x ULN and \> 20 x ULN

* Total bilirubin \> 2 x ULN

* ALP \> 1.5 x ULN

* Concurrent (within 1 day) ALT or AST \> 3 x ULN and total bilirubin \> 1.5 x ULN

* Concurrent (within 30 days) ALT or AST \> 3 x ULN and total bilirubin \> 1.5 x ULN

* Concurrent (within 1 day) ALT or AST \> 3 x ULN and total bilirubin \> 2 x ULN

* Concurrent (within 30 days) ALT or AST \> 3 x ULN and total bilirubin \> 2 x ULN

Number of Participants With Laboratory Values Change From BaselineFrom first dose to up to 30 days post last dose (Up to 34 months)

Number of participants changed from baseline in laboratory values of worst toxicity grade (grade 0= wnl, grade 1= mild, grade 2= moderate, grade 3= severe) based on US conventional units by cohort

Number of Participants With Laboratory Abnormalities in Specific Thyroid TestsFrom first dose to up to 30 days post last dose (Up to 34 months)

Number of participants with laboratory abnormalities in specific thyroid tests based on US conventional units. The number of participants with the following laboratory abnormalities from on-treatment evaluations will be summarized:

* TSH value \> ULN and

* with baseline TSH value \<= ULN

* with at least one FT3/FT4 test value \< LLN within 2-week window after the abnormal TSH test

* with all FT3/FT4 test values \>= LLN within 2-week window after the abnormal TSH test

* with FT3/FT4 missing within 2-week window after the abnormal TSH test.

* TSH \< LLN and

* with baseline TSH value \>= LLN

* with at least one FT3/FT4 test value \> ULN within 2-week window after the abnormal TSH test

* with all FT3/FT4 test values \<= ULN within 2-week window after the abnormal TSH test

* with FT3/FT4 missing within 2-week window after the abnormal TSH test

Number of DeathsUp to 36 months

Number of deaths in all treated participants

Trial Locations

Locations (66)

Local Institution - 0037

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Miami, Florida, United States

Local Institution - 0009

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Marietta, Georgia, United States

Local Institution - 0012

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Detroit, Michigan, United States

Local Institution - 0035

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Omaha, Nebraska, United States

Local Institution - 0036

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Daphne, Alabama, United States

Local Institution - 0010

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Rancho Mirage, California, United States

Local Institution - 0049

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New Haven, Connecticut, United States

Local Institution - 0065

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Louisville, Kentucky, United States

Tulane University

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New Orleans, Louisiana, United States

Local Institution - 0040

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Rockville, Maryland, United States

Boston Medical Center

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Boston, Massachusetts, United States

Local Institution - 0069

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Jackson, Mississippi, United States

Local Institution - 0011

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Saint Louis, Missouri, United States

Local Institution - 0038

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Albany, New York, United States

Local Institution - 0068

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New York, New York, United States

Local Institution - 0041

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Durham, North Carolina, United States

Local Institution - 0024

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Portland, Oregon, United States

Local Institution - 0053

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Allentown, Pennsylvania, United States

Local Institution - 0039

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Fairfax, Virginia, United States

Local Institution - 0052

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Caba, Buenos Aires, Argentina

Local Institution - 0042

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Capital Federal, Buenos Aires, Argentina

Local Institution - 0062

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Villa Siburu, Cordoba, Argentina

Local Institution - 0044

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Ciudad Autonoma de Buenos Aires, Distrito Federal, Argentina

Local Institution - 0043

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Caba, Argentina

Local Institution - 0015

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Camperdown, New South Wales, Australia

Local Institution - 0017

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Westmead, New South Wales, Australia

Local Institution - 0014

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South Brisbane, Queensland, Australia

Local Institution - 0016

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Elizabeth Vale, South Australia, Australia

Local Institution - 0050

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Clayton, Victoria, Australia

Local Institution - 0013

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Heidelberg, Victoria, Australia

Local Institution - 0020

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Belo Horizonte, Minas Gerais, Brazil

Local Institution - 0074

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Belo Horizonte, Minas Gerais, Brazil

Local Institution - 0075

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Curitiba, Parana, Brazil

Local Institution - 0018

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Ijui, RIO Grande DO SUL, Brazil

Local Institution - 0021

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Porto Alegre, Rio Grande Do Sul, Brazil

Local Institution - 0022

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Campinas, SAO Paulo, Brazil

Local Institution - 0071

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São Paulo, SAO Paulo, Brazil

Local Institution - 0019

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Rio de Janeiro, Brazil

Local Institution - 0073

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Sao Paulo, Brazil

Local Institution - 0067

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Kelowna, British Columbia, Canada

Local Institution - 0059

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Moncton, New Brunswick, Canada

Local Institution - 0055

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Hamilton, Ontario, Canada

Local Institution - 0066

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Montreal, Quebec, Canada

Local Institution - 0056

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Quebec City, Quebec, Canada

Local Institution - 0034

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Santiago, Metropolitana, Chile

Local Institution - 0051

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Vina del Mar, Valparaiso, Chile

Local Institution - 0027

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Monteria, Cordoba, Colombia

Local Institution - 0026

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Medellin, Colombia

Local Institution - 0033

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Besancon, France

Local Institution - 0032

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Clermont-ferrand, France

Local Institution - 0031

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Lyon, France

Local Institution - 0030

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Marseille, France

Local Institution - 0029

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Villejuif, France

Local Institution - 0001

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Essen, Germany

Local Institution - 0006

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Goettingen, Germany

Local Institution - 0004

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Heidelberg, Germany

Local Institution - 0002

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Jena, Germany

Local Institution - 0007

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Koblenz, Germany

Local Institution - 0064

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Muenchen, Germany

Local Institution - 0054

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Leon, Guanajuato, Mexico

Local Institution - 0061

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Guadalajara, Jalisco, Mexico

Local Institution - 0048

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Guadalajara, Jalisco, Mexico

Local Institution - 0025

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Culiacan, Sinaloa, Mexico

Local Institution - 0045

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Madrid, Spain

Local Institution - 0046

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Pamplona, Spain

Local Institution - 0047

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Sevilla, Spain

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