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Home » Newsletters » BioWorld

BioWorld

Dec. 19, 2013

View Archived Issues

Clinic Roundup

California Stem Cell Inc., of Irvine, Calif., completed a Phase I trial of a cancer stem cell-based therapy, DC-TC in hepatocellular carcinoma. The trial, carried out in Shanghai, China, in accordance with international standards, was designed to determine safety in patients with Stage IV disease. Read More

Financings Roundup

Synthetic Biologics Inc., of Rockville, Md., said it closed a its underwritten public offering of 13.225 million shares of its common stock, including a fully exercised over-allotment option by the underwriters covering 1,725,000 shares, offered at a price of $1 per share. The gross proceeds were $13.2 million. Read More

Pharma: Clinic Roundup

Merck & Co. Inc., of Whitehouse Station, N.J., is collaborating with Glaxosmithkline plc, of London, to test Merck’s anti-PD-1 immunotherapy, MK-3475, with GSK’s oral kinase inhibitor, pazopanib, in advanced renal cell carcinoma. The companies began a Phase I/II trial evaluating safety and efficacy of the compound in treatment-naïve patients with the disease. Under the collaboration, the companies will study MK-3475 with pazopanib and other agents in the GSK portfolio in the future. Read More

Pharma: Other News to Note

Perrigo Co. plc, of Allegan, Mich., completed its acquisition of Elan Corp., of Dublin, in a cash and stock transaction worth $8.6 billion. Perrigo and Elan have been combined under a new company incorporated in Ireland called Perrigo Company plc. Shares of the company will trade on the NYSE and Tel Aviv Stock Exchange under the ticker symbol PRGO. Read More

Other News to Note

Taiwan Liposome Co. Ltd. (TLC), of Taipei, Taiwan, signed a collaboration agreement with Sandoz AG, an affiliate in the generics division of Novartis AG, of Basel, Switzerland, giving Sandoz responsibility for commercialization of Liposomal Amphotericin B in the European Union and the U.S. Read More

Narcolepsy-flu link gives clues to disorder’s origin

Researchers have gained new insights into the autoimmune roots of narcolepsy – findings that will allow both easier diagnosis of the disorder, and “a model to understand other autoimmune disorders,” Stanford University’s Emmanuel Mignot told BioWorld Today. Read More

Depomed snaps up Nautilus migraine drug for $48.7M

Depomed Inc. boosted its pain portfolio with the purchase of Nautilus Neurosciences Inc.’s migraine drug, Cambia (diclofenac potassium for oral solution) for $48.7 million. Nautilus is eligible for an additional $5 million payment based on achievement of sales milestones. Cambia is the only single agent non-steroidal anti-inflammatory specifically indicated for migraine, with $18 million in sales over the past 3 months. Read More

SEC proposes rule to make Regulation A a viable route

Biotech start-ups may soon be able to travel a repaved Regulation A route to raise up to $50 million. Read More

Onconova’s pancreatic bid fizzles; rigosertib still alive in MDS

Heading for the end of the year, investors probably were looking for positive pivotal data from Onconova Therapeutics Inc.’s rigosertib in myelodysplastic syndromes (MDS); instead, the Newtown, Pa.-based biotech said Wednesday it was calling it quits on the Phase II/III trial testing the drug in pancreatic cancer. Read More

HCV regimen wins in Phase III; Street’s ‘ION’ Gilead pricing

Ribavirin (RBV) could drop out of hepatitis C virus (HCV) therapy for genotype 1 (GT1) patients, as a result of Gilead Sciences Inc.’s triumph in the Phase III program known as ION, which tested the once-daily, fixed-dose combination of its approved nucleotide analog polymerase inhibitor Sovaldi (sofosbuvir) and the NS5A inhibitor ledipasvir, with and without RBV. Read More

Stock Movers

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