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Bristol Myers Squibb Presents 56-Week Phase 3 Data in Pediatric Patients with Symptomatic Obstructive Hypertrophic Cardiomyopathy (oHCM) for Camzyos (mavacamten) at the Hypertrophic Cardiomyopathy Medical Society (HCMS) Scientific Sessions

Key Takeaway: Bristol Myers Squibb presented 56-week Phase 3 data for Camzyos (mavacamten) in pediatric patients with symptomatic obstructive hypertrophic cardiomyopathy (oHCM). The findings were shared at the Hypertrophic Cardiomyopathy Medical Society Scientific Sessions. This data highlights the potential effectiveness of Camzyos in this patient population.

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POSITIVE FACTORS

  • 56-week Phase 3 data presented
  • Focus on pediatric patients
  • Potential benefits of Camzyos in oHCM

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+19%
120-day peak, hindsight
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1.7%
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Mezigdomide
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Full Press Release Details

PRINCETON, N.J.--(BUSINESS WIRE)---- $BMY #AHA--Bristol Myers Squibb Presents 56-Week Phase 3 Data in Pediatric Patients with Symptomatic Obstructive Hypertrophic Cardiomyopathy for Camzyos...

Frequently Asked Questions

What is Camzyos used for?

Camzyos (mavacamten) is used to treat symptomatic obstructive hypertrophic cardiomyopathy.

What were the results of the Phase 3 study?

The study presented 56-week data showing potential benefits for pediatric patients.

Where was the data presented?

The data was presented at the Hypertrophic Cardiomyopathy Medical Society Scientific Sessions.

Who conducted the Phase 3 study?

The study was conducted by Bristol Myers Squibb.

Last updated: Nov 6, 2026