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Spots Global Cancer Trial Database for Investigation of Metformin in Patients With Castration Resistant Prostate Cancer in Combination With Enzalutamide vs. Enzalutamide Alone

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Trial Identification

Brief Title: Investigation of Metformin in Patients With Castration Resistant Prostate Cancer in Combination With Enzalutamide vs. Enzalutamide Alone

Official Title: Investigation of Metformin in Patients With Castration Resistant Prostate Cancer in Combination With Enzalutamide vs. Enzalutamide Alone (IMPROVE TRIAL): A Randomized, Open Label, Phase II Trial

Study ID: NCT02640534

Study Description

Brief Summary: The purpose of this trial is to test if the combination of enzalutamide and metformin in patients with castration resistant prostate cancer CRPC progressing on androgen deprivation therapy ADT is more effective compared to enzalutamide alone. The half of the patients will receive the experimental treatment combination, enzalutamide and metformin, while the other half will receive enzalutamide alone.

Detailed Description: One in seven men will be diagnosed with cancer of the prostate during his lifetime . Accordingly, prostate cancer (PC) is the most common cancer amongst men in the western world and worldwide. PC ranks second in cancer incidence and sixth in cancer mortality in men. The current standard of care for patients with metastatic castration resistant prostate cancer (mCRPC) and disease progression is either treatment with abiraterone acetate and prednisone in asymptomatic or mildly symptomatic patients without visceral metastases, or treatment with docetaxel in more symptomatic patients and in the presence of visceral metastases. Rothemundt et al. previously demonstrated favorable effects of metformin in a phase II trial: it yields objective Prostate specific antigen PSA responses and may induce disease stabilization and improve metabolic endpoints in patients with CRPC. Therefore addition of metformin to enzalutamide might have positive impact on tumor progression, on body composition, and insulin sensitivity.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: MALE

Healthy Volunteers: No

Locations

Kantonsspital Aarau, Aarau, , Switzerland

Universitaetsspital Basel, Basel, , Switzerland

Istituto Oncologico della Svizzera Italiana (IOSI), Bellinzona, , Switzerland

Kantonsspital Graubuenden, Chur, , Switzerland

Spital Thurgau AG, Frauenfeld, , Switzerland

Hôpitaux Universitaires de Genève, Genève 14, , Switzerland

CCAC Lausanne, Lausanne, , Switzerland

Luzerner Kantonsspital, Luzern 16, , Switzerland

Hôpital du Valais, Martigny, , Switzerland

Kantonsspital Olten, Olten, , Switzerland

Hôpital du Valais, Sion, , Switzerland

Bürgerspital Solothurn, Solothurn, , Switzerland

Kantonsspital St. Gallen, St. Gallen, , Switzerland

Kantonsspital Winterthur, Winterthur, , Switzerland

Stadtspital Triemli, Zürich, , Switzerland

UniversitätsSpital Zürich, Zürich, , Switzerland

Contact Details

Name: Christian Rothermundt, MD

Affiliation: Cantonal Hospital of St. Gallen

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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