The following info and data is provided "as is" to help patients around the globe.
We do not endorse or review these studies in any way.
Brief Title: Continuation of Drug Supply in Chinese Patients After CAMN107DBR01study Termination
Official Title: Continuation of Drug Supply in Chinese Patients After CAMN107DBR01study Termination
Study ID: NCT01613053
Brief Summary: Continuation of drug supply in Chinese patients after CAMN107DBR01study termination.
Detailed Description: Five patients who are on treatment of imatinib and deriving clinical benefit after CAMN107DBR01 study termination and written informed consent obtained will enter the trial, all five patients will receive Glivec (8oomg per day) treatment until tumor progression \[by RECIST guidelines, version 1.0\], unacceptable toxicity, death or withdrawal of consent.
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Novartis Investigative Site, Chengdu, Sichuan, China
Novartis Investigative Site, Guang zhou, , China
Novartis Investigative Site, Shanghai, , China
Name: Jie Zhong, M.D.
Affiliation: Ruijin Hospital of Shanghai Jiaotong University
Role: PRINCIPAL_INVESTIGATOR