Eiger doses first patient in phase 2 LIMT HDV study
LIMT HDV is a 30-patient study designed to evaluate the safety, tolerability and efficacy of two dose levels of Lambda after 48 weeks of treatment. LIMT HDV is
The US Food and Drug Administration (FDA) has accepted for review the supplemental biologics license application (sBLA) for Sanofi and Regeneron’s Dupixent (dupilumab) to treat chronic spontaneous urticaria (CSU) in adults and children aged 12 and above, particularly for those whose condition persists despite H1 antihistamine treatment.
Follitropin delta is the first recombinant follicle stimulating hormone (FSH) derived from a human cell line. It has been developed for individualized dosing depending on a woman’s serum