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Spots Global Cancer Trial Database for Efficacy Study of Sunitinib and Everolimus (Rotational vs Sequential Arm) in Pats. With m Clear Cell Renal Cancer

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Trial Identification

Brief Title: Efficacy Study of Sunitinib and Everolimus (Rotational vs Sequential Arm) in Pats. With m Clear Cell Renal Cancer

Official Title: Randomized ph. II Study to Explore Efficacy and Feasibility of Upfront Rotations Between SUNitinib and Everolimus vs Sequential Treatment of 1st lIne Sunitinib & 2nd Line EverolimuS Until Progression in Pats Met. Clear Cell Renal Cancer

Study ID: NCT01784978

Interventions

Sunitinib
Everolimus

Study Description

Brief Summary: The objective of this study is to assess the progression-free survival, of patients who receive rotations of sunitinib and everolimus versus patients who receive sunitinib as a first line treatment followed by everolimus when progression occurs.

Detailed Description: This is an open-label, randomized phase II study to investigate the feasibility of alternating cycles of treatment with sunitinib and everolimus compared to sequential treatment of sunitinib followed by everolimus. The study population consists of adult patients (over 18 years old) with clear cell mRCC (Metastatic Renal Cell Cancer) who have not received prior therapy for their metastatic disease. The purpose of the study is to determine the progression free survival, feasibility and safety profile of the experimental arm compared to standard of care. In the experimental arm alternating treatment will consist of repeating cycles of 24 weeks of treatment consisting of 12 weeks of sunitinib 4weeks on 2 weeks off, 50 mg pd followed by 12 weeks of everolimus 10 mg per day 11 weeks on 1 week off in patients with metastatic clear cell renal cancer. The comparative arm will be the standard regimen of sunitinib (50 mg pd 4/2) until progression, followed thereafter by everolimus (10 mg per day continuously, 11/1) until progression.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Hopital Bordeaux University, Bordeaux, , France

ALEXANDRA General Hospital of Athens, Athens, , Greece

Hospital Universitario Central de Asturias, Oviedo, Asturias, Spain

Hospital Marqués de Valdecilla, Santander, Cantabria, Spain

Hospital del Mar, Barcelona, , Spain

Hospital Universitario 12 de Octubre, Madrid, , Spain

Hospital Clínico San Carlos, Madrid, , Spain

Clara Campal. Hospital Sanchinarro, Madrid, , Spain

Hospital Universitario Virgen de la Victoria, Málaga, , Spain

Hospital General Universitario de Valencia, Valencia, , Spain

Contact Details

Name: Joaquim Bellmunt, MD/PhD

Affiliation: Associacio Per la Recerca Oncológica (APRO)

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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