Share Icon Health Study Area: Cardiovascular Disease Chevron Icon Health Study Area: Genitourinary For Patients Health Study Area: Lung Cancer Page Icon Phone Icon For Caregivers Health Study Area: AutoImmune Disease Health Study Area: Melanoma Location Icon Print YouTube Icon For Parents Health Study Area: Lung Cancer Print Created with Sketch. Help Icon Green Check Icon Search Icon Instagram Created with sketchtool. Direction Arrow Icon Error Icon For Parents Health Study Area: Blood Cancer Help Icon Health Study Area: NASH Gender Both Bookmark Icon Health Study Area: Melanoma Created with Sketch. Glossary Print Health Study Area: Blood Cancer Health Study Area: Genitourinary Health Study Area: Gastrointestinal Cancer Mobile Menu Icon Created with Sketch. Health Study Area: Cardiovascular Disease Health Study Area: Women's Cancer Communities Map Icon Created with Sketch. For Caregivers Health Study Area: Fibrosis Health Study Area: AutoImmune Disease FAQs Health Study Area: Head and Neck Cancer Created with Sketch. For Clinicians Chevron Right Icon Gender Female Health Study Area: Breast Cancer Direction Arrow Icon Gender Both Right Arrow Icon LinkedIn Icon Green Check Icon Gender Male Health Study Area: Fibrosis For Patients Twitter Icon Email Icon Facebook Icon Health Study Area: Gastrointestinal Cancer Health Study Area: Head and Neck Cancer For Clinicians External Link Icon
Hledat Study Connect

Recruiting

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

Updated: 16 říjen, 2024   |   ClinicalTrials.gov

Tisk přehledného shrnutí

ZVAŽUJETE TOTO HODNOCENÍ?
Vytiskněte si tuto stránku a průvodce hodnocením, pomůže vám to při rozhovoru s lékařem.
Pomocí průvodce hodnocením se můžete pohybovat procesem účasti na klinickém hodnocení. Než se rozhodnete, zjistěte si, jaké jsou klíčové faktory, a připravte si otázky pro zdravotnický tým.

Podrobnosti o hodnocení

  • Phase 2

    Fáze

  • Pohlaví

  • 18+

    Věková skupina

  • 37

    Umístění

  • Recruiting

Možnosti léčby

Ramena studie
Přiřazená léčba
Experimental: Adagrasib 400mg BID
Drug: Adagrasib
Experimental: Adagrasib 600mg BID
Drug: Adagrasib

Klíčová kritéria způsobilosti

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.

Důrazně doporučujeme kontaktovat BMS a oznámit vedlejší účinky / nežádoucí příhody
Zde jsou definovány vedlejší účinky / nežádoucí příhody a další příhody, které by měly být hlášeny
Nahlásit vedlejší účinky / nežádoucí příhody nebo stížnosti na kvalitu produktu: lékařské informace

Máte otázky? Pošlete nám e-mail

Máte otázky?
Pošlete nám e-mail