Safety and Effectiveness of ABM-168 in Adults with Advanced Solid Tumors.

PHASE1TerminatedINTERVENTIONAL
Enrollment

12

Participants

Timeline

Start Date

March 30, 2023

Primary Completion Date

June 30, 2024

Study Completion Date

June 30, 2024

Conditions
Advanced Solid TumorRAS MutationRAF MutationNF1 Mutation
Interventions
DRUG

ABM-168

Dosage: 0.5 mg; 2 mg; 6 mg; once daily by oral administration

Trial Locations (6)

46202

Indiana University Simon and Bren Simon Comprehensive Cancer Center, Indianapolis

75039

Next Oncology, Irving

77030

MD Anderson Cancer Center, Houston

84112

Huntsman Cancer Institute, University of Utah, Salt Lake City

94143

UCSF Helen Diller Family Comprehensive Cancer Center, San Francisco

08901

Rutgers Cancer Institute of New Jersey, New Brunswick

Sponsors
All Listed Sponsors
lead

ABM Therapeutics Corporation

INDUSTRY