For Healthcare Professionals

A Phase 1/2, Study Evaluating the Safety, Tolerability, PK, and Efficacy of Sotorasib (AMG 510) in Subjects With Solid Tumors With a Specific KRAS Mutation (CodeBreaK 100)

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About the study

Evaluate the safety and tolerability of sotorasib in adult subjects with KRAS p.G12C mutant advanced solid tumors. Estimate the maximum tolerated dose (MTD) and/or a recommended phase 2 dose (RP2D) in adult subjects with KRAS p.G12C mutant advanced solid tumors.
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Who can take part

You may be eligible to participate in the study if you meet the following criteria:

INCLUSION CRITERIA

Inclusion Criteria:


  1. Men or women greater than or equal to 18 years old.
  2. Pathologically documented, locally-advanced or metastatic malignancy with, KRAS p.G12C mutation identified through molecular testing.

EXCLUSION CRITERIA

Exclusion Criteria


  1. Active brain metastases from non-brain tumors.
  2. Myocardial infarction within 6 months of study day 1.
  3. Gastrointestinal (GI) tract disease causing the inability to take oral medication.

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Study Locations

Enter your ZIP code/Postal code/PIN code to locate study sites near you:

How to Apply


Contact the study center to learn if this study is a good match for you.

Study’s details


Contition

KRAS p.G12C Mutant Advanced Solid Tumors

Age (in years)

18 - 100

Phase

Phase 1/Phase 2

Participants needed

713

Est. Completion Date

Nov 8, 2027

Treatment type

Interventional


Sponsor

Amgen

ClinicalTrials.gov identifier

NCT03600883

Study number

20170543

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