Phase 2 Trial of Adagrasib Monotherapy and in Combination With Pembrolizumab and a Phase 3 Trial of Adagrasib in Combination in Patients With a KRAS G12C Mutation KRYSTAL-7
Metastatic Non-small Cell Lung Cancer | Advanced Non-Small Cell Lung CancerThe Phase 2 portion of this study evaluates the efficacy and safety of MRTX849 monotherapy and in combination with pembrolizumab in cohorts of patients with advanced NSCLC with KRAS G12C mutation and any PD-L1 TPS and who are candidates for first-line treatment.
The Phase 3 portion of the study compares the efficacy of adagrasib in combination with pembrolizumab versus pembrolizumab in patients with unresectable, locally advanced or metastatic nonsquamous NSCLC with KRAS G12C mutation and PD-L1 TPS \>=50% and who are candidates for first line treatment.
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Participation Requirements
-
Sex:
ALL -
Eligible Ages:
18 and up
Participation Criteria
Inclusion Criteria:
* Phase 2: Histologically confirmed diagnosis of unresectable or metastatic NSCLC with KRAS G12C mutation and any PD-L1 TPS
* Phase 3: Histologically confirmed diagnosis of unresectable or metastatic squamous or nonsquamous NSCLC with KRAS G12C mutation and PD-L1 TPS \>=50%
* Phase 3: Presence of evaluable or measurable disease per RECIST
* Phase 3: CNS Inclusion - Based on screening brain imaging, patients must have one of the following:
1. No evidence of brain metastases
2. Untreated brain metastases not needing immediate local therapy
3. Previously treated brain metastases not needing immediate local therapy
Exclusion Criteria:
* Phase 2 and Phase 3: Prior systemic treatment for locally advanced or metastatic NSCLC including chemotherapy, immune checkpoint inhibitor therapy, or a therapy targeting KRAS G12C mutation (e.g., AMG 510).
* Phase 2: Active brain metastases
* Phase 3: Patients with known central nervous system (CNS) lesions must not have any of the following:
1. Any untreated brain lesions \> 1.0 cm in size
2. Any brainstem lesions
3. Ongoing use of systemic corticosteroids for control of symptoms of brain lesions at a total daily dose of \> 10 mg of prednisone (or equivalent) prior to randomization.
4. Have poorly controlled (\> 1/week) generalized or complex partial seizures, or manifest neurologic progression due to brain lesions notwithstanding CNS-directed therapy
* Phase 3: Radiation to the lung \> 30 Gy within 6 months prior to the first dose of study treatment
Study Location
Local Institution - 007-489
Local Institution - 007-489London, Ontario
Canada
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British Columbia Cancer Agency - Vancouver
British Columbia Cancer Agency - VancouverVancouver, British Columbia
Canada
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Janessa Laskin, Site 007-480
111-111-1111Local Institution - 007-490
Local Institution - 007-490Montreal, Quebec
Canada
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Ottawa Hospital - General Campus
Ottawa Hospital - General CampusOttawa, Ontario
Canada
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Nicholas Garth, Site 007-481
6137377700Cross Cancer Institute
Cross Cancer InstituteEdmonton, Alberta
Canada
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Quincy Chu, Site 007-488
7804328248Princess Margaret Cancer Centre
Princess Margaret Cancer CentreToronto, Ontario
Canada
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Penelope Bradbury, Site 007-482
4169463544- Study Sponsored By
- Mirati Therapeutics Inc.
- Participants Required
- More Information
- Study ID:
NCT04613596