US FDA approves expanded indication for Supernus’ Qelbree for ADHD
Qelbree now received approval for ADHD treatment in children starting at the age of six, adolescents as well as adults. Supernus Pharmaceuticals president and CEO Jack Khattar said:
The US Food and Drug Administration (FDA) has accepted Bristol Myers Squibb’s (BMS) supplemental new drug application (sNDA) for Camzyos (mavacamten) to treat adolescents aged 12 to under 18 years with symptomatic obstructive hypertrophic cardiomyopathy (oHCM).
An orally disintegrating tablet and a calcitonin gene-related peptide (CGRP) receptor antagonist, Vydrua got the marketing authorisation for acute treatment of migraine with or without aura, and prophylaxis