A Study to Evaluate KIN-3248 in Participants With Advanced Tumors Harboring FGFR2 and//or FGFR3 Gene Alterations

PHASE1TerminatedINTERVENTIONAL
Enrollment

54

Participants

Timeline

Start Date

March 29, 2022

Primary Completion Date

October 3, 2024

Study Completion Date

October 3, 2024

Conditions
Solid Tumor, AdultIntrahepatic CholangiocarcinomaUrothelial Carcinoma
Interventions
DRUG

KIN-3248

KIN-3248 will be administered orally once daily in 28-day cycles

Trial Locations (21)

2100

Rigshospitalet (Copenhagen University Hospital) - Finsencentret - Onkologisk Klinik, Copenhagen

10016

NYU Langone Cancer Center, New York

11217

Veterans General Hospital - Taipei, Taipei

19111

Fox Chase Cancer Center, Philadelphia

28040

START (Fundacion Jimenez Diaz), Madrid

32224

Mayo Clinic Florida, Jacksonville

32827

Sarah Cannon Research Institute - Lake Nona, Orlando

37203

Sarah Cannon Research Institute, Nashville

49546

START Midwest, Grand Rapids

53705

University of Wisconsin Carbone Cancer Center, Madison

55905

Mayo Clinic Rochester, Rochester

77030

MD Anderson Cancer Center, Houston

80756

National Taiwan University Hospital, Taipei

Kaohsiung Medical University Hospital, Kaohsiung City

85054

Mayo Clinic Arizona, Phoenix

92093

UC San Diego Moores Cancer Center, La Jolla

100142

Beijing Cancer Hospital, Beijing

02214

Massachusetts General Hospital, Boston

03080

Seoul National University Hospital (SNUH), Seoul

03772

Severance Hospital Yonsei University Health System, Seoul

06351

Samsung Medical Center, Seoul

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Kinnate Biopharma

INDUSTRY