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Brief Title: First-in-man Dose Escalation Study of BAY1179470 in Patients With Advanced, Refractory Solid Tumors
Official Title: An Open-label, Phase I, Dose-escalation Study to Characterize the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Intravenous BAY 1179470 in Subjects With Advanced, Refractory Solid Tumors.
Study ID: NCT01881217
Brief Summary: An open-label, non-randomized, Phase I dose-escalation study designed to assess the safety, tolerability, pharmacokinetics(PK) /pharmacodynamics( PD) and tumor response profile of BAY1179470 in subjects with advanced, refractory solid tumors
Detailed Description:
Minimum Age: 20 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
, Kashiwa, Chiba, Japan
, Kita-Adachigun, Saitama, Japan
, Chuo-ku, Tokyo, Japan
, Koto-ku, Tokyo, Japan
, Fukuoka, , Japan
, Seoul, , Korea, Republic of
, Singapore, , Singapore
, Singapore, , Singapore
Name: Bayer Study Director
Affiliation: Bayer
Role: STUDY_DIRECTOR