Drug

Mavacamten

As of the edition of 20 October 2026, Mavacamten is a small molecule: marketed, first approved in 2022 (US); acts on MYH7; US protection ends in 2036.

Sources: FDA Orange Book and Purple Book, other approval registers, ClinicalTrials.gov, ChEMBL.

The drug

Status
Marketed; latest approval 2025
Kind
Small molecule
Brand name
Camzyos
First approved
28 April 2022 (US)
Approvals on record
11 in 5 regions
Holder of the most recent approval
Bristol Myers Squibb
Registered trials
41, 1 stopped early
Disease areas
Heart and blood vessels; Infections

US protection

US protection ends in 2036.

The last listed US drug-substance patent ends in 2036. The application that gives this date is held by Bristol Myers Squibb.

This is the US only, and it is not the date generics or biosimilars can enter.

The exact date and the listings behind it

In the product

16 listings count towards this date. The exact date and each listing are in the product.

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Target

GeneProteinUniProt
MYH7Myosin-7P12883

Registered trials

PhaseTrialsCompletedActiveStopped early
Phase not stated184140
Phase 18800
Phase 24400
Phase 37511
Phase 44040
All trials41

Who has held its approvals

CompanyRoleYears
Bristol Myers SquibbOriginator, Applicant and Lead sponsor of trials2014 to now