XTL Biopharmaceuticals amends licensing agreement with Presidio
Under the terms of the amended license agreement, XTL will receive an additional non-refundable payment of $2 million in return for reduction in future contingent payments. Under the
The US Food and Drug Administration (FDA) has granted rare paediatric disease designation to Vanda Pharmaceuticals’ VCA-894A, an investigational antisense oligonucleotide therapy for Charcot-Marie-Tooth disease, axonal, type 2S (CMT2S).
The Phase Ia single-center clinical trial evaluated the safety, tolerability, pharmacokinetic profile, and pharmacological activity of CR845 in a double-blind, randomized, placebo-controlled, single escalating intravenous dose study in
The patent covers, amongst others, compositions where the active ingredient is selected from mesalazine, budesonide, metformin, octylonium bromide, gabapentin, carbidopa, nimesulide, propionylcarnitine, isosorbide mono- and dinitrate, naproxen, ibuprofen,