A Phase 1/2, Open-Label, Dose-Escalation, Safety Study of INCAGN01949 in Subjects With Advanced or Metastatic Solid Tumors

PHASE1/PHASE2CompletedINTERVENTIONAL
Enrollment

87

Participants

Timeline

Start Date

October 31, 2016

Primary Completion Date

March 26, 2019

Study Completion Date

March 26, 2019

Conditions
Advanced MalignanciesMetastatic Cancer
Interventions
DRUG

INCAGN01949

Initial cohort dose of INCAGN01949 monotherapy at the protocol-defined starting dose, with subsequent cohort escalations based on protocol-specific criteria. The recommended dose will be taken forward into expansion cohorts.

Trial Locations (8)

1011

University Hospital of Laussane (CHUV), Lausanne

10016

New York University Clinical Cancer Center, New York

37232

Vanderbilt University Medical Center, Nashville

77030

MD Anderson Cancer Center, Houston

08901

Rutgers, The State University of New Jersey, New Brunswick

08035

Vall d'Hebron Institute of Oncology (VHIO), Barcelona

NW1 2PG

University College Hospital, London

OX3 7LE

University of Oxford, Oxford

All Listed Sponsors
lead

Incyte Biosciences International Sàrl

INDUSTRY