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Spots Global Cancer Trial Database for Study of Abiraterone Acetate Plus ADT Versus APALUTAMIDE Versus Abiraterone and APALUTAMIDE in Patients With Advanced Prostate Cancer With Non-castrate Testosterone Levels

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Trial Identification

Brief Title: Study of Abiraterone Acetate Plus ADT Versus APALUTAMIDE Versus Abiraterone and APALUTAMIDE in Patients With Advanced Prostate Cancer With Non-castrate Testosterone Levels

Official Title: Phase II Randomized Study of Abiraterone Acetate Plus ADT Versus APALUTAMIDE Versus Abiraterone and APALUTAMIDE in Patients With Advanced Prostate Cancer With Non-castrate Testosterone Levels

Study ID: NCT02867020

Conditions

Prostate Cancer

Study Description

Brief Summary: Evaluation of the activity, safety and patients reported outcome of ADT plus abiraterone, abiraterone plus APALUTAMIDE (a second-generation antiandrogen) or APALUTAMIDE alone in hormone naïve locally advanced or metastatic prostate cancer which ADT was indicated.

Detailed Description: Based on the current guidelines, ADT alone or combined with is antiandrogens are considered the appropriate active therapy for the patient population planned for this study. Recent data showed that chemotherapy also benefit patients in this setting. Even though, there is a clear unmet medical need for alternative treatment option in metastatic hormone sensitive prostate cancer (mHSPC). Treatments that can delay disease progression, and are associated with less comorbidities would be of significant clinical benefit in this patient population. The study is designed to assess the efficacy and safety of abiraterone plus APALUTAMIDE (a second-generation antiandrogen) or APALUTAMIDE alone without castration side effects and the other arm a combination of ADT and abiraterone; this last arm is to reflect an Abiraterone ongoing pivotal trial (LATITUDE), that assess the efficacy of adding abiraterone to castration in this setting of patients. Abiraterone had already showed clinical benefit in CRPC patients without prior chemotherapy.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: MALE

Healthy Volunteers: No

Locations

Clínica AMO, Salvador, Bahia, Brazil

CRIO, Fortaleza, Ceará, Brazil

Hospital Erasto Gaertner, Curitiba, Paraná, Brazil

Liga Norte Riograndense de Oncologia, Natal, Rio Grande Do Norte, Brazil

Hospital de Caridade de Ijuí, Ijuí, Rio Grande Do Sul, Brazil

CPO - Pucrs, Porto Alegre, Rio Grande Do Sul, Brazil

Oncologia Rede D'Or S.A., Rio de Janeiro, RJ, Brazil

Hospital de Câncer de Barretos, Barretos, São Paulo, Brazil

Centro de Pesquisa Clínica em Hematologia e Oncologia - CEPHO, Santo André, São Paulo, Brazil

Grupo COI, Rio de Janeiro, , Brazil

Beneficiencia Portuguesa de São Paulo/Hospital São José, São Paulo, , Brazil

Hospital Israelita Albert Einstein, São Paulo, , Brazil

IBCC, São Paulo, , Brazil

ICESP, São Paulo, , Brazil

Contact Details

Name: Fernando Maluf, MD

Affiliation: Beneficiência Portuguesa de São Paulo

Role: PRINCIPAL_INVESTIGATOR

Name: Gustavo Werutsky, MD

Affiliation: Latin American Cooperative Oncology Group

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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