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Home » Newsletters » BioWorld Asia

BioWorld Asia

Sep. 18, 2013

View Archived Issues

Circassia Seeks Backers for Phase III Allergy Therapy Study

LONDON – Circassia Ltd. is looking for shareholders’ backing for a Phase III trial of its house dust mite allergy treatment after reporting positive results in a Phase II study, with subjects who received the most effective dose showing a significant reduction in symptoms of allergic rhinitis at one year. Read More

UK Parliament: Raise the Curtain on Clinical Trial Data

LONDON – UK Members of Parliament (MPs) added their voices to the clamor for greater transparency of clinical trial results, describing the current situation as “unacceptable” and calling for the publication of clinical study reports and moves to provide controlled access to patient-level data. Read More

Chiesi Pulls Trigger on Cornerstone Purchase

Cornerstone Therapeutics Inc.’s largest shareholder, Italian pharma Chiesi Farmaceutici SpA, sweetened its original bid to purchase the specialty pharma’s remaining shares, settling on $9.50 each in cash. Read More

TCM Compound for IBS, Crohn’s Moves into Phase III Testing

SHANGHAI – A joint venture between a Chinese and a Swiss company has launched Phase III trials for a botanical drug to treat inflammatory bowel disease. Read More

Zealand Falls as Sanofi Delays GLP-1 NDA; Combo Drug on Track

Shares of Zealand Pharma A/S dropped 15.4 percent last Thursday after lixisenatide partner Sanofi SA said it decided to withdraw its new drug application (NDA) for the once-daily glucagon-like peptide-1 (GLP-1) receptor agonist in Type II diabetes mellitus, with plans to resubmit in 2015 after completing a cardiovascular outcomes trial. Read More

Other News To Note

• Alcobra Ltd., of Tel Aviv, Israel, reported preclinical results showing significant improvement in cognitive and social functioning following treatment of MG01CI (sustained-release metadoxine) in a mouse model of Fragile X syndrome. Read More

Screening Study Delivers a New Target for Cystic Fibrosis

LONDON – The prospects for new drugs to treat cystic fibrosis have improved, following a project to screen thousands of genes to determine which of their protein products affects the function of a molecular sodium channel found on cell membranes. Read More

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