Adare Pharmaceuticals Oral Drug Delivery Technologies and Drug Development

Adare Pharmaceuticals has officially opened a new corporate headquarters at 1200 Lenox Drive in Lawrenceville, New Jersey.

Global specialty pharmaceutical company Adare Pharmaceuticals will present its company overview at the BIO International Convention in California.

Sanofi K.K has announced that Allegra dry syrup 5% has launched in Japan.

Aptalis has signed a definitive agreement to be acquired by Forest Laboratories, a leading, fully integrated, specialty pharmaceutical company, for $2.9bn in cash pending required reviews.

Aptalis Pharmaceutical Technologies, a business unit of Aptalis Pharma that focuses on developing patient-optimised oral products utilising its proprietary pharmaceutical technologies and development expertise, hasa announced its co-sponsorship of Controlled Release Society's Young Investigator Award.

Aptalis Pharmaceutical Technologies, a business unit of Aptalis Pharma that develops differentiated products utilizing its oral delivery technologies, today announces that Nigel Ray has been named as the company's Vice President of Global Licensing.

Aptalis Pharmaceutical Technologies has released two free white papers on Pharmaceutical Technology.

Aptalis Pharmaceutical Technologies, formerly Eurand Pharmaceutical Technologies, focused on developing differentiated oral products utilising its pharmaceutical technologies, today announced that the European Commission has granted marketing authorisation for a new pediatric indication of a new oral granule formulation of Gilead Sciences's Viread® (tenofovir disoproxil fumarate) for HIV-1 infected children aged two to six years of age, and for HIV-1 infected children above six years of age for whom a solid dosage form is not appropriate.

FDA approvals, revenue gain and organic business growth are just a few of the topics that Aptalis Pharma president John Fraher addresses during an on-air interview with PharmaVentures and PharmaTelevision CEO Fintan Walton. The interview, conducted during BIO 2012 in Boston, reflects Fraher's commentary regarding the integration of companies post Axcan Intermediate Holdings' acquisition of Eurand NV in 2011.

Aptalis Pharmaceutical Technologies has announced its co-sponsorship of the Controlled Release Society's Young Investigator Award and its participation in the 39th Annual Meeting & Exposition of the Controlled Release Society.

Aptalis Pharmaceutical Technologies has released two new free-to-download white papers on Pharmaceutical Technology.

Aptalis (previously known as Eurand, Inc.), Cephalon, a wholly-owned subsidiary of Teva Pharmaceuticals Industries Ltd, and Anesta AG prevailed in their appeal to the U.S. Court of Appeals for the Federal Circuit, which reversed a lower court's determination and held that two patents covering the AMRIX muscle relaxant (Cyclobenzaprine Hydrochloride Extended-Release Capsules) are valid.

Aptalis Pharma has announced that the US Food and Drug Administration (FDA) has approved a new drug application (NDA) for Gilead Sciences' Viread® (tenofovir disoproxil fumarate) oral powder in combination with other antiretroviral agents for the treatment of HIV-1 infection in pediatric patients ages 2-5.

Company strategy, portfolio development and emerging markets are just a few of the topics that John Fraher, president of Aptalis Pharma, is scheduled to address during an on-air interview with Fintan Walton, CEO, PharmaVentures and PharmaTelevision. The interview is available via on-demand at Pha

At a time when difficult to formulate molecules and a decline of new chemical entities (NCEs) for new therapies have resulted in pipeline gaps, weakened product portfolios and a challenging R&D environment, the need to create products that address unmet medical needs and marketable advantages

Steve Ellul, Eurand's director of licensing, will discuss aspects of the company's growth strategy during the session 'Understanding the Drivers for Strategic Decision-Making' at BioEurope Spring in Milan, Italy, on Monday 14 March from 9am to 10.30am local time. The panel of industry

Eurand, a global specialty pharmaceutical company, and Nycomed, a privately owned global pharmaceutical company, have announced an exclusive commercialization, license and supply agreement for Russia and the Commonwealth of Independent States (CIS), as well as Georgia and Mongolia. Financial term

Eurand, a global specialty pharmaceutical company, has conducted a webinar titled 'The $10 Billion Gap: Leveraging Taste-Masking Technologies to Meet Global Patient Needs', presented by Troy Harmon, vice president of business development, and Andrew Thompson, vice president of commercial operatio

Eurand, a global specialty pharmaceutical company, today reported revenues for the second quarter of 2010 of €32.9m ($40.5m), an increase of 8%, or 3% in constant currency, from the second quarter of 2009. For the six months ended 30 June 2010, revenues totaled €64m ($78.7m), up

Eurand Pharmaceuticals, a subsidiary of global specialty pharmaceutical company Eurand, today announced additional data from a post-hoc analysis of a Phase III clinical trial with ZENPEP® (pancrelipase) delayed-release capsules, an FDA-approved pancreatic enzyme product (PEP) for the treatme

Eurand, a global specialty pharmaceutical company, today announced the appointment of Jean-Louis Anspach as president, Eurand Pharmaceuticals, Inc. (EPI). Anspach is a 25-year veteran of the specialty pharmaceutical and chemical industries and was most recently executive vice president, marketing

Eurand, a global specialty pharmaceutical company, announced today the grant of US Patent No. 7,658,918, titled 'Stable digestive enzyme compositions', by the United States Patent and Trademark Office (USPTO). The patent will provide Eurand with coverage until at least 20 February 2028 on ZENPEP&

Eurand, a specialty pharmaceutical company that develops enhanced pharmaceutical and biopharmaceutical products based on its proprietary pharmaceutical technologies, announced today that the Dutch Medicines Evaluation Board (MEB) informed the company that the decentralized procedure (DCP) for reg

Eurand, a specialty pharmaceutical company that develops enhanced pharmaceutical and biopharmaceutical products based on its proprietary pharmaceutical technologies, today announced that the US Food and Drug Administration (FDA) has approved EUR-1048, to be marketed as GlaxoSmithKline's Lamictal&

Eurand, a specialty pharmaceutical company, today announced the initiation of the second of two Phase III clinical trials required for registration of its Pancreatic Enzyme Product (PEP), EUR-1008, in patients with Exocrine Pancreatic Insufficiency (EPI). EPI is a deficiency of digestive enzymes