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Recruiting

Trial of Two Adagrasib Dosing Regimens in NSCLC With KRAS G12C Mutation (KRYSTAL 21) - CA239-0012

Oppdatert: 7 august, 2024   |   ClinicalTrials.gov

Utskriftsvennlig Sammendrag

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Vis detaljer

  • Phase 2

    Fase

  • Kjønn

  • 18+

    Aldersgruppe

  • 37

    Sted(er)

  • Recruiting

Behandlingsalternativer

Studiearmer
TILDELT INTERVENSJON
Experimental: Adagrasib 400mg BID
Drug: Adagrasib
Experimental: Adagrasib 600mg BID
Drug: Adagrasib

Nøkkelkriterier for kvalifikasjon

Key Inclusion Criteria: - Are at least 18 years old (or old enough to legally make their own treatment decisions, according to local laws). - Have advanced NSCLC or metastatic NSCLC (NSCLC that started in the lungs and then spread to other parts of the body) with the KRAS G12C mutation. - Have had previous treatment with 1) chemotherapy that included a drug called cisplatin or a drug called carboplatin and 2) a type of drug called an immune checkpoint inhibitor. - Have recovered from their prior treatment and blood tests are within a safe range. Key Exclusion Criteria: - Have had previous treatment with a drug that targets KRAS G12C. - Have cancer that can potentially be removed with surgery. - Patients with brain lesions are not eligible if 1) any untreated brain lesions are > 2.0 cm in size 2) any brainstem lesions are present 3) ongoing steroid dosing >10 mg daily prednisone (or equivalent) and 4) poorly controlled (> 1/week) generalized or complex partial seizures or neurologic progression/instability due to brain lesions. - Have certain medical conditions or need to take certain medications that, in the opinion of a trial doctor, could make it unsafe for them to participate or difficult to complete the trial assessments, or are pregnant.

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Bivirkninger (uønskede hendelser) og andre rapporterbare hendelser er definert her
For å rapportere bivirkninger (uønskede hendelser) eller reklamere på et legemiddel: Medisinsk informasjon

MLTNO2000046