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BioWorld - Friday, March 20, 2026
Home » Newsletters » BioWorld Asia

BioWorld Asia

Oct. 24, 2012

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Biotechnology Trust Reports Strong Investor Returns

LONDON – International Biotechnology Trust (IBT) reported strong returns for shareholders, driven by new drug approvals, high levels of merger and acquisition activity and the resilience of leading biotech companies in the current growth-stunting environment. Read More

Study: Cancer Cell Proteins Join Forces to Achieve Movement

LONDON – A protein that determines how well cells can move and spread could provide a new target for drug designers who want to prevent metastasis of cancer cells. Read More

Summit Moving Lead Drugs with Wellcome Trust Award

LONDON – Summit plc is making headway with its two lead programs, winning a £4 million (US$6.42 million) translation award from the Wellcome Trust for clinical trials of SMT19969, a narrow-spectrum antibiotic for treating Clostridium difficile infections, and starting Phase II development of SMT-C1100, a treatment for Duchenne's muscular dystrophy (DMD). Read More

French Consortium Investing $104M in Cell Therapy Facility

Aided by a generous dollop of government cash, a French consortium of biotechnology companies and academic medical centers is investing €80 million (US$104 million) to develop an industrial-scale facility for the production of cell therapy, including stem cell therapy. Read More

Covagen Inks $146M Fynomer Discovery Pact with Mitsubishi

Covagen AG signed its first drug discovery deal last week, a pact worth potentially up to €112.25 million (US$146 million) with Mitsubishi Tanabe Pharma Corp. that involves its Fynomer protein scaffold technology. Read More

OctoPlus Shares Surge After Dr. Reddy's $36M Buyout Bid

The management of Dutch drug delivery specialist OctoPlus NV agreed to a €27.4 million (US$35.8 million) cash offer from Indian generics firm Dr. Reddy's Laboratories Ltd. Read More

PAH Space Getting Hotter as Actelion Files Macitentan NDA

LONDON – There's a race to market for a new generation of pulmonary arterial hypertension (PAH) drugs with Actelion Ltd. announcing it has filed for FDA approval of Opsumit (macitentan) and Bayer Healthcare revealing positive Phase III data for riociguat and promising global filings in the first half of 2013. Read More

Other News To Note

• Chiesi Group, of Parma, Italy, said it completed a Phase I trial of inhaled PDE4 inhibitor CHF 6001 that showed the drug was well tolerated up to the highest doses administered, in single and multiple dose parts of the study. Read More

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