Press Room

Press Release / Jun 14, 2011

Hovione announces filing of patent for new powder inhaler

Hovione announced today the international filing of its latest patent covering a new, highly efficient dry powder inhaler (DPI), XCaps.

XCaps fills a void in the pulmonary inhalation market, as a device which combines high efficiency in powder dispersion with ease of use. Lung fractions in excess of 70% have been achieved, from a device which only requires two steps to inhalation and which only has two components plus a dust cover. This makes XCaps highly suited for inhalation applications where minimal training of patients is desirable and has the versatility to treat almost all pulmonary diseases, including asthma, COPD and infection. 

XCaps follows on the heels of another successful Hovione DPI, TwinCaps®, which was developed specifically for an influenza application and is licensed to Daiichi Sankyo and Biota for this application. Daiichi Sankyo launched Inavir® in the Japanese market in October 2010 and monthly sales in Japan of this TwinCaps®-delivered neuraminidase inhibitor since then have surpassed those of Roche’s Tamiflu® (1, 2).

Hovione is offering XCaps in optional conjunction with its drug product development program, allowing potential licensees to take their candidate drugs from the API stage all the way to the unit dose, under one roof. “We give our customers an edge in speed of development because we are perhaps the only independent company developing DPIs with expertise in every aspect of the inhaled drug development process”, said Peter Villax, Vice-President and co-inventor of the device.

Phil Nelson, Business Development Manager, said “Hovione has wide-ranging expertise in the field of inhalation products. With our core API process development and manufacturing expertise, we can manufacture pharmaceutical ingredients where the final crystallization step produces pulmonary delivery-friendly particles. Alternatively, we can use other particle formulation technologies, such as spray-drying and we are currently pioneering new particle technologies for stable, large dose delivery.” Hovione is currently executing inhaled drug development projects for 5 pharmaceutical companies, involving API process development, particle engineering, formulation and clinical supplies.
 

About Hovione

Hovione is an international company with over 50 years’ experience in Active Pharmaceutical Ingredient development and compliant manufacture. With four FDA inspected sites in the U.S., China, Ireland, and Portugal, the company focuses on the most demanding customers, in the most regulated markets. The company also offers integrated API, particle design and formulation development and manufacturing. In the inhalation area, Hovione is the only independent company offering such a broad range of services. 

More about XCaps at www.hovione.com 

Sources:
  1. https://www.biota.com.au/uploaded/154/1021733_76openbriefing-ceoonoutlo.pdf  
  2. FY2010 Consolidated Financial Overview, Chugai Pharmaceutical Co. Ltd., February 2, 2011
Contacts at Hovione

Phil Nelson, PhD
Business Development Manager
pnelson@hovione.com
+351 219 847 619

Isabel Pina
Corporate Communications
ipina@hovione.com
+351 21 982 9362

 

 

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Hovione is bringing momentum to the intranasal field after announcing that its lead single-use nasal dry powder device, developed in collaboration with Industrial Design Consultancy Ltd (IDC), is now available for commercial partnerships. The milestone marks the transition from prototype to a fully integrated intranasal drug delivery platform that spans Hovione’s end-to-end partnership capabilities–from API synthesis through advanced formulation and particle engineering to drug product manufacturing, including device supply and advanced analytical tools for nasal performance characterization. The platform’s single-use device is designed to be manufacturable at scale and to leverage existing advanced particle engineering and drug product manufacturing capabilities, a practical advantage that can shorten timelines to clinic and commercialization while reducing development risk and cost. The device’s patented mechanism supports targeted nasal deposition, including access to the upper olfactory region. This enables rapid systemic absorption and potential nose-to-brain delivery pathways that are increasingly important for CNS and emergency-use indications. Beyond the single-use format, Hovione and IDC are advancing a multi-dose variant to broaden applicability across dosing regimens and therapeutic areas. The collaboration is backed by an intellectual property portfolio and initial patent grants, positioning the platform as a turnkey option for pharma partners seeking a single integrated supplier for both drug substance and device. This development arrives as intranasal delivery gains traction for systemic, CNS and rapid-onset therapies. This is precisely the focus of the upcoming 4th Nasal Formulation & Delivery Summit, for which Hovione is a key sponsor. The annual summit unites formulation, delivery and product development leaders to tackle drug-device compatibility, translational preclinical models, and strategies for scalable, regulatory-ready intranasal programs. Hovione’s recent progress will be highly relevant to attendees looking to de-risk nose-to-brain and systemic intranasal programs. Read the full article at News-Medical.net    

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