Miraculins signs licensing agreement with Mount Sinai Hospital
Under the terms of the agreement, Miraculins will issue to Mount Sinai Hospital (MSH) 310,000 common shares from treasury, subject to a standard four-month and one day resale
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).
The milestone was triggered by Progenics’s initiation of a Phase I clinical trial with its prostate-specific membrane antigen (PSMA)-targeted antibody-drug conjugate (ADC) for patients with hormone-refractory prostate cancer.