Valeant, Kaken sign license deal to develop new chemical entity for psoriasis
If approved, KP-470 will represent a novel drug with an alternate mechanism of action in the topical treatment of the disease. Under the terms of the licensing agreement,
Teva Pharmaceutical has announced the US Food and Drug Administration (FDA) approval for Ponlimsi (denosumab-adet) as a biosimilar to Prolia, alongside the acceptance of its biosimilar candidate applications for Xolair (omalizumab) by both the agency and the European Medicines Agency (EMA).
Lusutrombopag (S-888711) is an investigational, once-daily, orally administered, small molecule thrombopoietin (TPO) receptor agonist. In the US, Shionogi is seeking FDA approval of lusutrombopag for the treatment of thrombocytopenia
The Alkindi patent, entitled "Treatment of Adrenal Insufficiency", is a pharmaceutical composition-of-matter patent protecting Alkindi's proprietary formulation as a treatment for adrenal insufficiency in paediatric and elderly adult