Indus Obtains FDA Approval For AIDS Molecule Trials
The US Food and Drug Administration (USFDA) has approved Indus Biotech to conduct clinical trails for its molecule, IND02, reported The Economic Times. The newly developed molecule is

The US Food and Drug Administration (USFDA) has approved Indus Biotech to conduct clinical trails for its molecule, IND02, reported The Economic Times. The newly developed molecule is

Solvay Pharmaceuticals has announced that new data demonstrate that Creon (pancrelipase) delayed-release capsules improves a key measure of fat absorption in adults with exocrine pancreatic insufficiency (EPI) due

Pharmaceutical design specialist Protomed has brought together key figures from the pharma, healthcare and pharmacy arenas to debate the future of medication management (22 October). Following recent news

SuperGen and GlaxoSmithKline have entered into a multi-year collaboration to discover and develop cancer therapeutics based on epigenetic targets. Under the terms of the deal, SuperGen will progress

NPS Pharmaceuticals has reported additional data from a phase 3 study supporting the efficacy of Gattex (teduglutide) in patients with parenteral nutrition (PN)-dependent short bowel syndrome (SBS). Data

Horizon Therapeutics has presented an analysis from two pivotal phase 3 trials (REDUCE-1 and REDUCE-2) evaluating its investigational compound HZT-501, a combination of ibuprofen with high-dose famotidine. The

The US Patent and Trademark Office (USPTO) has notified ExonHit of its intent to issue a re-examination certificate in connection with ExonHit’s US Patent n° 6881571 directed to

Pharmalink has been granted Japanese Patent No 4326696, for its product Nefecon. It is being developed to treat IgA nephropathy. Counterparts of the patent have been issued for

Merck KGaA has announced that group total revenues rose 2.7% in the third quarter to E1,944m from E1,893m in the year-ago quarter. The group’s operating result declined by

Ranbaxy Laboratories, an Indian major, has posted net sale of $356m for Q3, 2009, a de-growth of 18% over Q3, 2008. EBITDA was $45m, a margin of 13%