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As previously disclosed, in January 2016 Novartis informed GenVec that enrollment in the trial had been paused in accordance with criteria in the trial's protocol.  In April 2016,

The Bill & Melinda Gates Foundation led the financing with an $8M investment followed by $2M each from existing investors Merck, Lilly Asia Ventures and ARCH Venture Partners. The proceeds

The ULTRA study will evaluate the effects of ubenimex in patients with secondary lymphedema of the lower limb(s) who are optimized on physical therapies.  Physical therapies, such as

All Series A investors contributed to the financing extension, including Alexandria Venture Investments, Bay City Capital LLC, Lundbeckfond Ventures, New Enterprise Associates (NEA), and Pfizer Venture Investments. Together

The phase 1/2 clinical trial will evaluate the safety, tolerability, and efficacy of BMS’s Opdivo and Opdivo + Yervoy in conjunction with AbbVie’s Rova-T, a delta-like protein 3

Valeant has received a complete response letter (CRL) from the FDA for latanoprostene bunod (LBN) ophthalmic solution 0.024%, an intraocular pressure lowering single-agent eye drop for patients with

The Onivyde, which is also known as nal-IRI or MM-398, in combination with 5-fluorouracil (5-FU) and leucovorin (LV), has been recommended, for the treatment of metastatic adenocarcinoma of

The once-daily Truvada (emtricitabine 200 mg/tenofovir disoproxil 245 mg) in combination with safer sex practices is intended to lower the risk of sexually acquired HIV-1 infection among uninfected

At the same time, the FDA has granted Fast Track designation to the compound’s development program for the treatment of CDI. MCB3837 is the IV prodrug of MCB3681,