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This recommendation follows the DSMB’s review of the safety data accumulated in the first eight (8) Alström syndrome patients that had received treatment with PBI-4050. The DSMB determined

NovaDerm, which recently received its orphan-drug designation from the FDA, is a regenerative cell therapy that has the potential to re-grow a patient’s own skin in a laboratory

BCD-085 is an innovative drug containing a humanized monoclonal anti-interleukin-17 (anti-IL17) antibody as an active ingredient. The primary objective of the international multicenter double-blind placebo-controlled study is to

RXi is a clinical-stage RNAi firm focused on the development of new therapeutics to solve significant unmet medical needs. As per the deal terms, RXi would issue stock

The aim of the study was to determine the safety and clinical benefit fexapotide can provide to men who were given a second injection of fexapotide for their

The trial showed SUTENT extended disease-free survival (DFS) by more than one year versus placebo in patients who were at high risk for recurrence after surgical resection of

Following the strategic partnership entered between the two companies in 2014 to combine resources and scientific expertise within dermatology development, the parties have now agreed to fully leverage

The sBLA is based on results from the Phase III RADIANCE study that demonstrated treatment with Lucentis provided superior visual acuity gains in people with mCNV compared to

Under the collaboration deal, Transgene will sponsor a phase 1/2 study to assess its therapeutic vaccine candidate TG4001 together with Merck and Pfizer's immunotherapy avelumab to treat human