A Study to Evaluate INCA036873 in Participants With Advanced Solid Tumors and Hematological Malignancies
Start Date
1/8/2026
Completion Date
8/18/2028
Summary
A study to evaluate the safety and tolerability of INCA036873 in participants with advanced solid tumors and hematological malignancies.
Eligibility Criteria
Age Range: 18 years to No maximum
Interventions
INCA036873
Conditions
Locations
City of Hope Medical Center
Duarte, California 91010
United States
University of California San Diego Medical Center, Moores Cancer Center
La Jolla, California 92037
United States
University of Michigan
Ann Arbor, Michigan 48109
United States
The University of Nebraska Medical Center
Omaha, Nebraska 68198
United States
Memorial Sloan Kettering Cancer Center
New York, New York 10021
United States
Scri Oncology Partners
Nashville, Tennessee 37203
United States
Vanderbilt Medical Center
Nashville, Tennessee 37232
United States
Md Anderson Cancer Center
Houston, Texas 77030
United States
Macquarie University Hospital
Sydney, New South Wales 02109
Australia
Princess Alexandra Hospital Australia
Woolloongabba, Queensland 04102
Australia
Cancer Research Sa
Adelaide, South Australia 05000
Australia
Peter Maccallum Cancer Centre-Royal Melbourne Hospital
Melbourne, Victoria 03000
Australia
Cliniques Universitaires Ucl Saint-Luc
Brussels, 01200
Belgium
Universitair Ziekenhuis Antwerpen
Edegem, 02650
Belgium
Universitair Ziekenhuis Gent (Uz Gent)
Ghent, 09000
Belgium
Universitair Ziekenhuis Leuven
Leuven, 03000
Belgium
Aarhus University Hospital
Aarhus, 08200
Denmark
Rigshospitalet Uni of Hospital of Copenhagen
Copenhagen, DK-2100
Denmark
Aou Policlinico S. Orsola-Malpighi
Bologna, 40138
Italy
Fondazione Irccs Istituto Nazionale Dei Tumori
Milan, 20133
Italy
Policlinico Universitario Agostino Gemelli Universita Cattolica Del Sacro Cuore
Rome, 00168
Italy
Centro Ricerche Cliniche Di Verona
Verona, 37134
Italy