This is a Phase 1/2, open-label, multicenter, study evaluating the safety, tolerability, PK, PD, and anti-tumor activity of MRTX0902 alone and in combination with MRTX849 (adagrasib) in patients with advanced solid tumor malignancy harboring mutations in the KRAS-MAPK pathways.
This first-in-human clinical trial will begin with an exploration of MRTX0902 dose and regimen. Once safety experience and PK data are available for the monotherapy regimen, dose escalation of the combination of MRTX0902 and adagrasib will be initiated, and will include a separate preliminary food effect assessments on MRTX0902 PK in combination with adagrasib. As potentially viable regimens are identified, Phase 1b expansion cohorts may be implemented to ensure collection of sufficient safety and PK information, and early evidence of clinical activity are available to recommend Phase 2 regimens. In Phase 2, separate cohorts of patients by histological diagnosis and/or baseline characteristics will be evaluated for the clinical activity and efficacy of MRTX0902 in combination with adagrasib.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
228
Local Institution - 001-108
New Haven, Connecticut, United States
Local Institution - 001-119
Newark, Delaware, United States
Phase 1: Number of Patients who Experience Dose-Limiting Toxicity
Time frame: 21 Days
Phase1/1B: Number of patients who experience a treatment-related adverse event
Time frame: Up to 2 years
Phase 2: Objective response rate (ORR)
Time frame: 2 years
Phase 2: Duration of response (DOR)
Time frame: 2 years
Phase 2: Progression free survival (PFS)
Time frame: 2 years
Phase 2: Overall survival (OS)
Time frame: 2 years
Area under the plasma concentration versus time curve
AUC - MRTX0902 and adagrasib
Time frame: Up to 4 days
Time to achieve maximal plasma concentration
Tmax - MRTX0902 and adagrasib
Time frame: Up to 4 days
Maximum observed plasma concentration
Cmax - MRTX0902 and adagrasib
Time frame: Up to 4 days
Terminal elimination half-life
t1/2 - MRTX0902
Time frame: Up to 4 days
Apparent total plasma clearance when dosed orally
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Local Institution - 001-111
Orlando, Florida, United States
Local Institution - 001-103
Baltimore, Maryland, United States
Local Institution - 001-110
Rochester, Minnesota, United States
Local Institution - 001-115
Hackensack, New Jersey, United States
Local Institution - 001-106
Cincinnati, Ohio, United States
Local Institution - 001-109
Portland, Oregon, United States
Local Institution - 001-116
Pittsburgh, Pennsylvania, United States
Local Institution - 001-101
Nashville, Tennessee, United States
...and 8 more locations
CL/F - MRTX0902
Time frame: Up to 4 days
Apparent volume of distribution when dosed orally
Vz/F - MRTX0902
Time frame: Up to 4 days