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Spots Global Cancer Trial Database for Refametinib(BAY86-9766) in RAS Mutant Hepatocellular Carcinoma (HCC)

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Trial Identification

Brief Title: Refametinib(BAY86-9766) in RAS Mutant Hepatocellular Carcinoma (HCC)

Official Title: A Prospective, Single-arm, Multicenter, Uncontrolled, Open-label Phase II Trial of Refametinib (BAY86-9766) in Patients With RAS Mutant Hepatocellular Carcinoma (HCC)

Study ID: NCT01915589

Study Description

Brief Summary: This is a study to investigate the potential clinical benefit of refametinib in patients with unresectable or metastatic HCC carrying a RAS mutation. The study will be conducted in 2 stages. Approximately 95 patients (15 at Stage 1/ 80 at Stage 2) will be accrued to this study to receive treatment. Stage 2 of the trial will only be conducted if at least 5 out of 15 patients at Stage 1 show at least confirmed partial response (PR) according to modified response evaluation criteria in solid tumors (mRECIST) assessed by central image review. Refametinib is an oral (i.e. taken by mouth) protein kinase inhibitor. A kinase inhibitor targets certain key proteins that are essential for the survival of the cancer cell. By specifically targeting these proteins, refametinib may stop cancer growth. The growth of the tumor may be decreased by preventing these specific proteins from functioning. The primary endpoint (the most meaningful result to be tracked) of this study is based on the rate of response, i.e. the disease getting smaller. The aim is to show that the therapy with refametinib improves the response rate in this RAS mutation patient population.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

, Washington, District of Columbia, United States

, Miami, Florida, United States

, Tampa, Florida, United States

, New York, New York, United States

, Rochester, New York, United States

, Graz, , Austria

, Bruxelles - Brussel, , Belgium

, Bruxelles - Brussel, , Belgium

, Charleroi, , Belgium

, Gent, , Belgium

, Leuven, , Belgium

, Praha 2, , Czechia

, CLERMONT-FERRAND Cedex 1, , France

, Creteil, , France

, Lille, , France

, Marseille, , France

, Montpellier Cedex, , France

, Vandoeuvre-les-nancy, , France

, Heidelberg, Baden-Württemberg, Germany

, München, Bayern, Germany

, Hannover, Niedersachsen, Germany

, Essen, Nordrhein-Westfalen, Germany

, Mainz, Rheinland-Pfalz, Germany

, Berlin, , Germany

, Shatin, , Hong Kong

, Budapest, , Hungary

, Debrecen, , Hungary

, Milano, Lombardia, Italy

, Milano, Lombardia, Italy

, Kashiwa-shi, Chiba, Japan

, Kobe, Hyogo, Japan

, Moriguchi, Osaka, Japan

, Osaka-shi, Osaka, Japan

, Osakasayama-shi, Osaka, Japan

, Sunto, Shizuoka, Japan

, Shimotsuke, Tochigi, Japan

, Chuo-ku, Tokyo, Japan

, Osaka, , Japan

, Shizuoka, , Japan

, Busan, , Korea, Republic of

, Daegu, , Korea, Republic of

, Seoul, , Korea, Republic of

, Seoul, , Korea, Republic of

, Seoul, , Korea, Republic of

, Auckland, , New Zealand

, Santiago de Compostela, A Coruña, Spain

, Barcelona, Catalunya, Spain

, Alicante, , Spain

, Pontevedra, , Spain

, Valencia, , Spain

, Genève 14, Genève, Switzerland

, Bern, , Switzerland

, Kaohsiung City, , Taiwan

, Tainan, , Taiwan

, Bangkok, , Thailand

, Bangkok, , Thailand

, Bangkok, , Thailand

, Birmingham, West Midlands, United Kingdom

Contact Details

Name: Bayer Study Director

Affiliation: Bayer

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

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