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Spots Global Cancer Trial Database for 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

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Trial Identification

Brief Title: 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

Official Title: A Phase 2 Trial of Adagrasib Monotherapy and in Combination With Pembrolizumab and a Phase 3 Trial of Adagrasib in Combination With Pembrolizumab Versus Pembrolizumab in Patients With Advanced Non-Small Cell Lung Cancer With KRAS G12C Mutation

Study ID: NCT04613596

Study Description

Brief Summary: The 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.

Detailed Description: The Phase 2 portion of this study will evaluate the efficacy and safety of MRTX849 as monotherapy and in combination with pembrolizumab. There will be 3 cohorts of patients, all of whom have KRAS G12C mutation, have advanced or metastatic NSCLC, and are candidates for first-line treatment. 2 cohorts have PD-L1 TPS score \<1% and are randomized to MRTX849 monotherapy or MRTX849 in combination with pembrolizumab. The 3rd cohort has PD-L1 TPS score of 1% or higher and is treated with MRTX849 and pembrolizumab The Phase 3 portion of the study will randomize patients with squamous or nonsquamous NSCLC with KRAS G12C mutation and TPS \>=50% in the first-line setting to adagrasib plus pembrolizumab or pembrolizumab. Primary efficacy objective is to compare efficacy between experimental and comparator arms. Secondary and exploratory objectives include evaluation of secondary efficacy endpoints, safety and tolerability, adagrasib PK, PROs, and correlative genomic biomarkers for the combination regimen in the study population. MRTX849 is an orally available small molecule inhibitor of KRAS G12C, and Pembrolizumab (KEYTRUDA®) is a humanized monoclonal antibody that blocks the interaction between PD-1 and its ligands, PD-L1 and PD-L2.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Research Site, Prescott Valley, Arizona, United States

Research Site, Tucson, Arizona, United States

Research Site, Springdale, Arkansas, United States

Research Site, Anaheim, California, United States

Research Site, Long Beach, California, United States

Research Site, Los Alamitos, California, United States

Research Site, San Francisco, California, United States

Research Site, San Francisco, California, United States

Research Site, Santa Rosa, California, United States

Research Site, Stockton, California, United States

Research Site, Whittier, California, United States

Research Site, Lone Tree, Colorado, United States

Research Site, Norwich, Connecticut, United States

Research Site, Bay Pines, Florida, United States

Research Site, Fort Myers, Florida, United States

Research Site, Fort Myers, Florida, United States

Research Site, Jacksonville, Florida, United States

Research Site, Jacksonville, Florida, United States

Research Site, Miami, Florida, United States

Research Site, Orlando, Florida, United States

Research Site, Pensacola, Florida, United States

Research Site, Tallahassee, Florida, United States

Research Site, Tampa, Florida, United States

Research Site, West Palm Beach, Florida, United States

Research Site, Athens, Georgia, United States

Research Site, Chicago, Illinois, United States

Research Site, Niles, Illinois, United States

Research site, Park Ridge, Illinois, United States

Research Site, Goshen, Indiana, United States

Research Site, Wichita, Kansas, United States

Research Site, Lexington, Kentucky, United States

Research Site, Covington, Louisiana, United States

Research Site, Baltimore, Maryland, United States

Research Site, Boston, Massachusetts, United States

Research Site, Burnsville, Minnesota, United States

Research Site, Jackson, Mississippi, United States

Research Site, Omaha, Nebraska, United States

Research Site, Las Vegas, Nevada, United States

Research Site, East Brunswick, New Jersey, United States

Research Site, Hackensack, New Jersey, United States

Research Site, Albany, New York, United States

Research Site, Bronx, New York, United States

Research Site, Durham, North Carolina, United States

Research Site, Cincinnati, Ohio, United States

Research Site, Cleveland, Ohio, United States

Research Site, Columbus, Ohio, United States

Research Site, Kettering, Ohio, United States

Research Site, Eugene, Oregon, United States

Research Site, Salem, Oregon, United States

Research Site, Tigard, Oregon, United States

Research Site, Sioux Falls, South Dakota, United States

Research Site, Germantown, Tennessee, United States

Research Site, Nashville, Tennessee, United States

Research Site, Amarillo, Texas, United States

Research Site, Arlington, Texas, United States

Research Site, Austin, Texas, United States

Research Site, Bedford, Texas, United States

Research Site, Dallas, Texas, United States

Research Site, Denison, Texas, United States

Research Site, Fredericksburg, Texas, United States

Research Site, The Woodlands, Texas, United States

Research Site, Tyler, Texas, United States

Research Site, Fairfax, Virginia, United States

Research Site, Richmond, Virginia, United States

Research Site, Wollongong, New South Wales, Australia

Research Site, Woolloongabba, Queensland, Australia

Research Site, Bedford Park, South Australia, Australia

Research Site, Ballarat, Victoria, Australia

Research Site, Klagenfurt, Carinthia, Austria

Research Site, Linz, , Austria

Research Site, Vienna, , Austria

Research Site, Edegem, Antwerpen, Belgium

Research Site, Gent, Vlaams Brabant, Belgium

Research Site, Hasselt, , Belgium

Research Site, Edmonton, Alberta, Canada

Research Site, Vancouver, British Columbia, Canada

Research Site, Ottawa, Ontario, Canada

Research Site, Toronto, Ontario, Canada

Research site, Hořovice, Central Bohemian, Czechia

Research Site, Olomouc, , Czechia

Research Site, Ostrava, , Czechia

Research Site, Praha, , Czechia

Research Site, Esslingen, Baden-Wuerttemberg, Germany

Research Site, Kempten, Bavaria, Germany

Research Site, Munchen, Bayern, Germany

Research Site, Kassel, Hessen, Germany

Research Site, Großhansdorf, Schleswig-Holstein, Germany

Research Site, Lübeck, Schleswig-Holstein, Germany

Research Site, Frankfurt, , Germany

Research Site, Gießen, , Germany

Research Site, Hemer, , Germany

Research Site, Oldenburg, , Germany

Research Site, Budapest, , Hungary

Research Site, Budapest, , Hungary

Research Site, Budapest, , Hungary

Research Site, Gyöngyös, , Hungary

Research Site, Torokbalint, , Hungary

Research Site, Dublin, , Ireland

Research Site, Afula, , Israel

Research Site, Be'er Sheva, , Israel

Research Site, Haifa, , Israel

Research Site, Jerusalem, , Israel

Research Site, Jerusalem, , Israel

Research Site, Reẖovot, , Israel

Research Site, Safed, , Israel

Research Site, Meldola, Forli-Cesena, Italy

Research Site, Bari, , Italy

Research Site, Bologna, , Italy

Research Site, Genova, , Italy

Research Site, Milan, , Italy

Research Site, Milan, , Italy

Research Site, Napoli, , Italy

Research Site, Parma, , Italy

Research Site, Roma, , Italy

Research Site, Rome, , Italy

Research Site, Varese, , Italy

Research Site, Incheon, Gyeonggi-do, Korea, Republic of

Research Site, Suwon-si, Gyeonggi-do, Korea, Republic of

Research Site, Busan, , Korea, Republic of

Research Site, Cheongju-si, , Korea, Republic of

Research Site, Daegu, , Korea, Republic of

Research Site, Goyang-si, , Korea, Republic of

Research Site, Seoul, , Korea, Republic of

Research Site, Seoul, , Korea, Republic of

Research Site, Amsterdam, Noord-Holland, Netherlands

Research Site, Rotterdam, Zuid-Holland, Netherlands

Research Site, Harderwijk, , Netherlands

Research Site, Utrecht, , Netherlands

Research Site, Gdańsk, Gdansk, Poland

Research Site, Lublin, , Poland

Research Site, Otwock, , Poland

Research Site, Skorzewo, , Poland

Research Site, Toruń, , Poland

Research Site, Lisbon, , Portugal

Research Site, Porto, , Portugal

Research Site, L'Hospitalet De Llobregat, Barcelona, Spain

Research Site, A Coruña, La Coruña, Spain

Research Site, Barcelona, , Spain

Research Site, Barcelona, , Spain

Research Site, Barcelona, , Spain

Research Site, Barcelona, , Spain

Research Site, Madrid, , Spain

Research Site, Madrid, , Spain

Research Site, Madrid, , Spain

Research Site, Madrid, , Spain

Research Site, Málaga, , Spain

Research Site, Santiago De Compostela, , Spain

Research Site, Sevilla, , Spain

Research Site, Valencia, , Spain

Research Site, Valencia, , Spain

Research Site, Tainan City, , Taiwan

Research Site, Birmingham, England, United Kingdom

Research Site, Guildford, England, United Kingdom

Research Site, London, England, United Kingdom

Research Site, Manchester, England, United Kingdom

Research Site, Leicester, , United Kingdom

Contact Details

Name: Barbara Wamil, MD

Affiliation: Mirati Therapeutics Inc.

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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