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BioWorld - Saturday, July 25, 2026
Home » Newsletters » BioWorld Asia

BioWorld Asia

May 2, 2012

View Archived Issues

Other News To Note

• Clinuvel Pharmaceuticals Ltd., of Melbourne, Australia, said two leading health insurers in Switzerland agreed to fully reimburse the cost of Scenesse (afamelanotide 16-mg implant) for erythropoietic protoporphyria, a rare disease characterized by severe phototoxicity. Read More

FDA Dings the Takeda/Furiex Type II Diabetes Combo

The FDA issued a complete response letter to Takeda Pharmaceutical Co. Ltd. last week regarding new drug applications for alogliptin and fixed-dose combinations of alogliptin and pioglitazone for Type II diabetes, products partnered with Furiex Pharmaceuticals Inc. Read More

ABPI: Cost Savings Shouldn't Trump Health Care Innovation

LONDON – The industry in the UK is hitting back at government cuts to the drugs bill, setting up a task force to liaise with National Health Service (NHS) payers and promote the use of innovative drugs. Read More

Seeking Greater Coordination, EMA Forms Another Committee

Faced with an increasingly complex system of committees, which threatens to undermine the coherence of pharmaceutical regulation in Europe, the European Medicines Agency (EMA) has come up with the perfect bureaucratic response: establish another committee. Read More

AstraZeneca's CEO Exits as Firm Enters Patent Cliff Free Fall

LONDON – AstraZeneca plc is expected to boost dealmaking and M&A activity after CEO David Brennan gave in to pressure from shareholders last week and agreed to resign his post. Read More

Study Suggests New Strategy to Treat Pancreatic Cancer

LONDON – The search for additional genes that play a role in the development of pancreatic cancer has uncovered a new tumor suppressor gene that has, until now, been overlooked. Read More

EUSA Swings Ideal Exit with $700M Acquisition by Jazz

The privately held UK specialty oncology firm EUSA Pharma Ltd. is to be acquired by Jazz Pharmaceuticals Inc. in a $700 million cash deal that is motivated by the early commercial success of EUSA's Erwinaze treatment for pediatric acute lymphoblastic leukemia (ALL), approved by the FDA in November 2011. Read More

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