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The phase 2 trial, dubbed Evolve, involved 14 patients ages 40 to 80 years who were undergoing percutaneous transluminal renal angioplasty and stenting. The study's endpoints were a change in

According to approval from the FDA’s Center for Biologics Evaluation and Research, the treatment can now be used among infants of six months or older. Before this approval,

CCH is marketed as XIAFLEX in the US and Xiapex in Europe. BioSpecifics' partner Endo International carried out the phase 2b trial, which enrolled 375 adult women with moderate or severe

The policy statement was informed by an FTC workshop held last year to examine how such drugs are marketed to consumers. The FTC also released its staff report

The financing from a single family office that is an existing investor includes the sale of a $1 million convertible note and up to $10 million in future equity

MEDI2070 is an IL-23 monoclonal antibody currently in a Phase IIb clinical trial for moderate-to-severe Crohn’s disease and ready for Phase II for ulcerative colitis, diseases that sit

Sirukumab is being co-developed by Janssen Biologics (Ireland) and GSK. The companies unveiled results from two pivotal phase 3 studies assessing subcutaneous (SC) sirukumab, a human anti-interleukin (IL)-6

APX001 has received orphan drug designation for four distinct indications: the treatment of invasive candidiasis, invasive aspergillosis, coccidioidomycosis, and rare mold infections caused by Scedosporium spp., Fusarium spp.,

har Pharmaceuticals focused on transforming IV-only drugs into oral drugs for existing and new indications using its proprietary technology EnhanceTM development platform. With this acquisition, Grünenthal has obtained