Taro’s Keveyis get FDA approval to treat primary hyperkalemic and hypokalemic periodic paralysis
Both are a group of rare hereditary disorders that cause episodes of muscle weakness or paralysis. The drug is the first to be approved by the FDA to
Axsome Therapeutics has received the US Food and Drug Administration (FDA) approval for Auvelity (dextromethorphan HBr and bupropion HCl) to treat agitation associated with dementia due to Alzheimer’s.
These autoimmune disorders include psoriasis, psoriatic arthritis, ankylosing spondylitis, rheumatoid arthritis and multiple sclerosis, as well as numerous orphan indications. The company intends to conduct this multiple ascending
B-701 is a new human monoclonal antibody specific for fibroblast growth factor receptor 3 (FGFR3) that is being developed to target FGFR3-positive tumors. The randomized, double-blinded, placebo-controlled, multicenter,