Scenesse Reduces Phototoxic Reactions In EPP Patients: Clinuvel Pharma
Clinuvel Pharma claimed that it had to develop new study methodology along with EPP experts to be able to evaluate Scenesse, in this 12 month European and Australian
HAYA Therapeutics has secured fast track designation from the US Food and Drug Administration (FDA) for its investigational therapy, HTX-001, to treat symptomatic non-obstructive hypertrophic cardiomyopathy (nHCM).
Making use of HighRes dual NanoCell system, which includes two AmbiStore high-speed carousels of HighRes, Rigel is expected to perform cell-based, biochemical, and high-content screening assays against a
As per the terms of the agreement, OctoPlus is expected to perform process development and clinical manufacturing for The Medicines Company related to MDCO-216 (ApoA-I Milano/phospholipid complex). MDCO-216