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Study of LY3537982 in Cancer Patients With a Specific Genetic Mutation (KRAS G12C)

Clinicaltrials.gov ID

NCT04956640

Status

Recruiting

Study Type

Interventional, Phase 1

Sponsor

Eli Lilly and Company

Start Date

19 juillet 2021

Anticipated End Date

30 septembre 2025

Study Contact

Name: Patient Advocacy

Phone Number:855-569-6305

Email: clinicaltrials@loxooncology.com

About the Study

The purpose of this study is to find out whether the study drug, LY3537982, is safe and effective in cancer patients who have a specific genetic mutation (KRAS G12C). Patients must have already received or were not able to tolerate the standard of care, except for specific groups who have not had cancer treatment. The study will last up to approximately 4 years.

Conditions

  • Carcinoma, Non-Small-Cell Lung

  • Colorectal Neoplams

  • Endometrial Neoplasms

  • Ovarian Neoplasms

  • Pancreatic Neoplasms

  • Biliary Tract Neoplasms

Inclusion/Exclusion Criteria?

Primary, Secondary, Other Outcome Measures??

Locations in Canada

  • Cross Cancer Institute, Edmonton, Alberta, T6G 1Z2, Canada

  • Princess Margaret Hospital, Toronto, Ontario, M5G 2M9, Canada

About the Study

The purpose of this study is to find out whether the study drug, LY3537982, is safe and effective in cancer patients who have a specific genetic mutation (KRAS G12C). Patients must have already received or were not able to tolerate the standard of care, except for specific groups who have not had cancer treatment. The study will last up to approximately 4 years.

Conditions

  • Carcinoma, Non-Small-Cell Lung

  • Colorectal Neoplams

  • Endometrial Neoplasms

  • Ovarian Neoplasms

  • Pancreatic Neoplasms

  • Biliary Tract Neoplasms

Interventions

DRUG:

  • LY3537982

  • Abemaciclib

  • Pembrolizumab

  • LY3295668

  • Cetuximab

  • Pemetrexed

  • Cisplatin

  • Carboplatin

Locations in Canada

  • Cross Cancer Institute, Edmonton, Alberta, T6G 1Z2, Canada

  • Princess Margaret Hospital, Toronto, Ontario, M5G 2M9, Canada

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Le Collectif Canadien pour le cholangiocarcinome (C3) est financé par une subvention d'équipe révolutionnaire de la Société Canadienne du cancer en partenariat avec les Instituts de recherche en santé du Canada. Les fonds de la subvention pour le C3 sont gérés par l'Institut de recherche de l'Hôpital d'Ottawa, qui sert d'institut principal pour toutes les opérations collaboratives.

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