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BioWorld - Saturday, December 13, 2025
Home » Newsletters » BioWorld

BioWorld

June 18, 2014

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Galapagos investors get jittery on GLPG634 delay, GLPG974 failure

Galapagos NV gave its investors some wobbles during its R&D day in New York Tuesday, revealing that its first-in-class, free fatty acid receptor 2 (FFA2) inhibitor, GLPG974, failed to demonstrate clinical benefit in ulcerative colitis and that recruitment delays will push back top-line data from two phase IIb trials of selective JAK1 inhibitor GLPG634 in rheumatoid arthritis patients. Read More

The wait is over for crucial FDA guidance on social media use

That social media guidance drugmakers have been clamoring for over the past five years? It's finally here. Two draft guidances dealing with social media issues are scheduled for publication in Wednesday's Federal Register. Read More

Novartis ex-employee arrested, offices raided in Diovan scandal

TOKYO ­– The controversy in Japan surrounding Novartis Pharma KK's blood pressure drug Diovan (valsartan) grew more intense over the last week following the arrest of a former employee and a raid of the company's offices. Read More

EIB investing $102M in UCB R&D pipeline in risk-sharing model

LONDON – The European Investment Bank (EIB) is to put in €75 million (US$101.8 million) to directly fund six research programs at pharma company UCB SA, as part of a new "at-risk co-development funding" instrument under which the bank will invest €24 billion in R&D projects over the next seven years. Read More

Serenus Biotherapeutics looks to tap Africa's underdeveloped market

Sub-Saharan Africa's economic takeoff has carried a growing number of the region's 1.1 billion people ahead on a wave of innovation, bringing new advances in mobile commerce, bioagriculture and green energy. Innovative drugs from the West, however, have arrived much more slowly. Read More

Nice 'complement': True North series A inspires $22M for rare diseases

Ipierian Inc. spinout True North Therapeutics Inc. will use $22 million from its series A round to push TNT009, its lead candidate, through early stage studies in autoantibody-driven rare diseases mediated by the complement system. Read More

Silenseed seeks $36.4M IPO to develop RNAi-based cancer drugs

Silenseed Ltd. followed hot on the heels of Vascular Biogenics Ltd. (VBL) to become the fourth Israeli biotech this year to seek a listing on a U.S. exchange. Filing as an emerging growth company, Silenseed is seeking to raise up to $36.4 million in its initial public offering (IPO) and to list on Nasdaq as RNAI. Read More

Ablynx's nanobody approach successful in phase II TTP trial

LONDON – Ablynx NV's caplacizumab is in line to be the first drug for treating rare blood coagulation disorder acquired thrombotic thrombocytopenic purpura (TTP), after the company reported positive phase II results. Read More

Other news to note

Discovery Laboratories Inc., of Warrington, Pa. realized the final $1.9 million of a $2.4 million fast track SBIR grant from the National Heart, Lung, and Blood Institute. Read More

In the clinic

GW Pharmaceuticals plc, of London, said physician reported efficacy and safety data on 27 children and young adults with treatment-resistant epilepsy who have been treated with GW's investigational cannabidiol product candidate, Epidiolex, for a period of 12 weeks. Read More

Stock movers

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Pharma: Other news to note

Boehringer Ingelheim GmbH, of Ingelheim, Germany, and Eli Lilly and Co., of Indianapolis, said they resubmitted the new drug application for sodium glucose co-transporter-2 inhibitor empagliflozin for the treatment of adults with type 2 diabetes. Read More

Pharma: In the clinic

Takeda Pharmaceuticals Co. Ltd., of Osaka, Japan, and H. Lundbeck A/S, of Copenhagen, reported data from a head-to-head study of Brintellix (vortioxetine) vs. escitalopram in patients with well-treated major depressive disorder experiencing treatment-emergent sexual dysfunction. Read More

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