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Home » Newsletters » BioWorld

BioWorld

March 23, 2015

View Archived Issues

Aducanumab, AD still golden for Biogen Idec in updated phase I findings

It's increasingly difficult to generate a big move in shares of a big biotech, but Alzheimer's disease (AD) did the trick again for Biogen Idec Inc., which continued to report upbeat findings for aducanumab (BIIB037) at the 12th International Conference on Alzheimer's and Parkinson's Diseases and Related Neurological Disorders in Nice, France. Read More

Malin, Nordic Nanovector raise $415M in upsized Dublin, Oslo offering

DUBLIN – Investor appetite for European biotech shows no sign of relenting, as Malin Corp. plc and Nordic Nanovector ASA priced their respective IPOs Friday, which will take in $415 million in total. Read More

Lilly strikes $456M oncology deal with China's Innovent

Eli Lilly and Co. is tapping China's Innovent Biologics Inc. to develop and manufacture a strategic portfolio of potential cancer therapies in one of the largest biotech collaborations between a multinational and a domestic drugmaker in China to date. Read More

Court: BPCIA 'patent dance' merely an optional safe harbor

The patent dance laid out in the Biologics Price Competition and Innovation Act (BPCIA) is merely a temporary safe harbor that biosimilar sponsors may opt out of, a federal district judge ruled last week in denying Amgen Inc.'s request for a temporary injunction and partial summary judgment to halt the U.S. launch of Sandoz Inc.'s Zarxio, a biosimilar to Amgen's blockbuster Neupogen. Read More

Protein shake-up in PD: Anti-synuclein's phase I results boost Prothena

Unlike Alzheimer's disease (AD), which took much of the spotlight Friday, "there's not another gene to argue over" in Parkinson's disease (PD), said CEO Dale Schenk, commenting on Prothena Corp. plc's phase I success with PRX002, which takes aim at alpha-synuclein. Read More

No free lunch between mosquitoes and GMOs

Genetically modified foods have the dubious distinction of being the scientific topic with the widest opinion gap between scientists and the lay public. In a report on "Public and Scientists' Views about Science and Society," 88 percent of scientists, but only 37 percent of the general public, believed that genetically modified foods were generally safe to eat. Read More

Ascletis' triple therapy HCV drug nails phase II trial in Chinese patients

SHANGHAI – Upstart domestic biotech Ascletis Inc., with offices in the U.S. and China, is a step closer to realizing its dream of having the first effective hepatitis C virus (HCV) treatment on the market in China. Read More

'Most Promising Drugs of 2015' span gamut of companies, indications

An annual forecast of drugs expected to debut in the coming year and eventually reach blockbuster status suggests the biopharma industry is not only alive and well but also not solely reliant on compounds that target the narrower indications implicit in precision medicine efforts. Read More

Stock movers

Read More

Regulatory front

The FDA is terminating the Antiviral Drugs Advisory Committee, according to a notice published in the Federal Register. No reason was given for the termination, with the notice simply stating that the committee "is no longer needed and was terminated on Feb. 15, 2015." Read More

Financings

Tekmira Pharmaceuticals Corp., a Vancouver, British Columbia-based company developing a potentially curative regimen for chronic hepatitis B virus infection upsized its public offering to 7.5 million common shares from an earlier 6 million, priced at $20.25 per share, for gross proceeds of $151.9 million. Read More

Other news to note

Batu Biologics Inc., of San Diego, said the rationale and preclinical data for its immunotherapeutic product, Vallovax, was published in the Journal of Translational Medicine. Read More

In the clinic

Cerulean Pharma Inc., of Cambridge, Mass., reported that an ongoing phase Ib/II trial of its lead nanoparticle-drug conjugate, CRLX101, in combination with Avastin (bevacizumab, Roche AG) in relapsed renal cell carcinoma (RCC) achieved its primary endpoint of at least 50 percent of patients achieving four months of progression-free survival (PFS). Read More

Pharma: In the clinic

Boehringer Ingelheim GmbH, of Ingelheim, Germany, reported phase II data showing that BI 655066 resulted in nearly double the percentage of patients with moderate to severe plaque psoriasis achieving clear or almost clear skin after 12 weeks of treatment, compared to Stelara (ustekinumab, Johnson & Johnson) (77.1 percent vs. 40 percent). Read More

Bench Press: BioWorld looks at translational medicine

Scientists from the German Heinrich Heine University have shown that the over-the-counter cough syrup dextromethorphan improved the function of pancreatic beta cells in mice and humans with type II diabetes. Read More

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