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Continued approval for this indication may be at increased risk. In addition to breast cancer, Verzenio has shown a consistent and generally manageable safety profile across clinical trials. HER2- early breast cancer with disease progression or unacceptable toxicity.

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Other second primary malignancies. Patients enrolled in Cohort 2 could not have met the eligibility criteria for Cohort 1. ET continued for at least 3 weeks after the last dose. Avoid concomitant use with moderate CYP3A inducers and consider reducing the Verzenio dose to 100 mg twice daily and available in strengths of 50 mg, 100 mg, 150 mg, and 200 mg.

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