Phase I, Dose-escalation Trial of BAY1187982 in Subjects With Advanced Solid Tumors Known to Express Fibroblast Growth Factor Receptor 2 (FGFR2)

PHASE1TerminatedINTERVENTIONAL
Enrollment

20

Participants

Timeline

Start Date

March 24, 2015

Primary Completion Date

July 27, 2016

Study Completion Date

July 27, 2016

Conditions
Medical Oncology
Interventions
DRUG

BAY1187982

A dose of 0.1 mg BAY 1187982 per kilogram (kg) body weight (BW) was chosen as the starting dose based on toxicology data. The investigational drug will be administered as a 1-hour IV infusion once every 21 days at the trial site (Day 1 of each 21-day Cycle). The maximum possible dose escalation will be 2-fold and not more than 0.5 mg/kg BW until maximum tolerated dose is selected

Trial Locations (13)

10016

New York

21231

Baltimore

37232

Nashville

60611

Chicago

63110

St Louis

77030

Houston

94115

San Francisco

169610

Singapore

90404-1200

Santa Monica

06520

New Haven

98109-1023

Seattle

03080

Seoul

138-736

Seoul

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Bayer

INDUSTRY