First-in-Human Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Mirvetuximab Soravtansine in Adults With Ovarian Cancer and Other Folate Receptor 1 (FOLR1)-Positive Solid Tumors

PHASE1CompletedINTERVENTIONAL
Enrollment

206

Participants

Timeline

Start Date

June 28, 2012

Primary Completion Date

March 19, 2018

Study Completion Date

March 19, 2018

Conditions
Tumors
Interventions
DRUG

Mirvetuximab soravtansine

Mirvetuximab soravtansine IV infusion will be administered as per dose and schedule specified in the respective arms.

Trial Locations (12)

10065

Memorial Sloan Kettering Cancer Center, New York

19111

Fox Chase Cancer Center, Philadelphia

37203

Sarah Cannon Research Institute, Nashville

43210

Ohio State University, Columbus

48201

Barbara Ann Karmanos Cancer Institute, Detroit

66205

University of Kansas Medical Center Research Institute, Fairway

73104

University of Oklahoma Stephenson Cancer Center, Oklahoma City

78229

CTRC at the University of Texas Health Science Center, San Antonio

02062

Massachusetts General Hospital, Boston

02115

Dana Farber Cancer Institute, Boston

M5G 2M9

Princess Margaret Hospital, Toronto

H4A3J1

McGill University Health Centre, Montreal

Sponsors

Lead Sponsor

All Listed Sponsors
lead

ImmunoGen, Inc.

INDUSTRY