Bristol-Myers, uniQure enter cardiovascular gene therapy deal
The deal will give BMS exclusive access to uniQure’s gene therapy technology platform for the development of new treatments. The companies will collaborate on up to ten targets,
The US Food and Drug Administration (FDA) has expanded the approved indication for Bristol Myers Squibb’s (BMS) Camzyos (mavacamten) to treat symptomatic obstructive hypertrophic cardiomyopathy (oHCM) in adults and paediatric patients weighing at least 30kg (66lb).
Initially, the Japanese firm will develop NBI-98854 in Japan for the chorea associated with Huntington’s disease (HD) and tardive dyskinesia. Complete commercial rights to NBI-98854 in North America,