Rexam has announced the decision to sell all three divisions of its Healthcare business: Pharmaceutical Devices, Prescription Retail Packaging and Closures & Containers. Montagu Private Equity has made an offer of $805 million for the Pharmaceutical Devices and Prescription Retail Packaging divisions, and Rexam says it is in talks to sell the Closures & Containers … [Read more...] about Rexam selling healthcare business, including OINDP manufacturing
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Chattem launches Nasacort Allergy 24HR nasal spray in US
Sanofi US consumer healthcare division Chattem has announced that Nasacort Allergy 24HR Nasal Spray is now available over the counter in the United States. The FDA approved the triamcinolone acetonide nasal spray as an OTC treatment for allergies in October 2013. Chattem CEO Zan Guerry commented, “Now that Nasacort Allergy 24HR is available over-the-counter, the … [Read more...] about Chattem launches Nasacort Allergy 24HR nasal spray in US
Mark Iwicki named President and CEO of Civitas
Civitas Therapeutics has announced that former Sunovion CEO Mark Iwicki will succeed Glenn Batchelder as President and Chief Executive Officer. Iwicki was most recently CEO of Blend Therapeutics. According to Civitas, which is developing inhaled drugs based on its proprietary ARCUS particle manufacturing and delivery platform, Batchelder will continue to serve on the … [Read more...] about Mark Iwicki named President and CEO of Civitas
Avanir submits NDA for dry powder intranasal sumatriptan
According to Avanir Pharmaceuticals, the company has submitted a 505(b)(2) New Drug Application (NDA) for its AVP-825 intranasal dry powder sumatriptan for the treatment of migraine to the FDA. Avanir acquired the North American license for the product from OptiNose in July 2013. The product uses OptiNose's delivery device, which uses the patient's breath to … [Read more...] about Avanir submits NDA for dry powder intranasal sumatriptan
Romania approves AirFluSal Forspiro
Romania has approved the 50 µg/500 µg dose version of Sandoz's AirFluSal Forspiro salmeterol/fluticasone DPI for the treatment of asthma and COPD, triggering a €1.5 million milestone payment to Vectura. The inhaler has also been approved recently by Denmark, Germany, Sweden, and Hungary. Read the Sandoz press release. … [Read more...] about Romania approves AirFluSal Forspiro
Copley Scientific launches new MDI testing products
Copley Scientific has announced the launch of its BAC 2000 breath actuated controller and BRS 1100 breathing simulator for the testing of MDIs with spacers and valved holding chambers in accordance with draft US Pharmacopoeia (USP) monograph . Together, the breath actuated controller and breathing simulator provide testing conditions representative of a range of … [Read more...] about Copley Scientific launches new MDI testing products
Phase 2 study of Prosonix drug-only glycopyrronium MDI produces positive results
Prosonix has announced that a Phase 2 clinical study of its PSX1002 glycopyrronium bromide MDI in 37 COPD patients demonstrated statistically significant improvement in lung function compared to placebo for a range of doses. PSX1002 is a drug-only suspension formulation created using Prosonix's proprietary particle engineering technology. The study also showed … [Read more...] about Phase 2 study of Prosonix drug-only glycopyrronium MDI produces positive results
Positive Phase 2b results for Evoke intranasal gastroparesis drug
Evoke Pharma has published a Phase 2b study demonstrating superior efficacy of intranasal metoclopramide compared to oral metoclopramide for the management of diabetic gastroparesis symptoms. The study appears in an upcoming issue of Neurogastroenterology & Motility and appears online ahead of publication. The six-week open-label, parallel design study involved 89 … [Read more...] about Positive Phase 2b results for Evoke intranasal gastroparesis drug
Spain moving toward Flutiform approval
Skyepharma has announced that Spain has completed a mutual recognition procedure regarding Flutiform fluticasone propionate/formoterol fumarate MDI for the treatment of asthma. The European Commission approved Flutiform in July 2012. The company also said that its European partner Mundipharma plans to launch the product in Spain after pricing and reimbursement have … [Read more...] about Spain moving toward Flutiform approval
Vivaldi and NIAID sign agreement on intranasal flu vaccine
Vivaldi Biosciences has signed an agreement with the NIH's National Institute of Allergy and Infectious Diseases (NIAID) for co-research and development of live attenuated influenza vaccine (LAIV) candidates against the H7N9 strain of influenza A. The company says that it and NIAID will work together to create LAIVs using H7N9 genes inserted into Vivaldi's master … [Read more...] about Vivaldi and NIAID sign agreement on intranasal flu vaccine