Press Room

Press Release / Nov 03, 2010

Hovione Wins Flumethasone Patent Case

(Lisbon, Portugal and New York, NY)—Hovione and Dickstein Shapiro LLP are pleased to announce that the U.S. Patent and Trademark’s Board of Patent Appeals and Interferences has reconfirmed Hovione's patent claims to a method of making flumethasone and its 17-carboxyl androsten analogue, two key intermediates on the synthesis of fluticasone, an important corticosteroid used in asthma medications, reversing a rejection by the reexamination examiner. The inter parties reexamination appeal decision, which found in favor of each of the firm’s arguments, was issued on October 26, 2010.

“We are pleased that the board agreed with our demonstration that the method claimed in Hovione’s patent was not obvious, despite the attempt by a competitor to show otherwise,” said Edward Meilman, partner in Dickstein Shapiro’s Intellectual Property Practice. Mr. Meilman handled the reexamination proceeding on behalf of Portugal-based international pharmaceutical company, Hovione.

Reexamination is a procedure in which a patent is reconsidered in light of prior art not previously considered during the original patenting procedure. Competitors often use this procedure in an effort to eliminate the patent entirely or limit it to a procedure which can be avoided. U.S. Patent Office statistics indicate that about half of reexamined patents do not meet the statutory requirement that a patented invention be unobvious. The board here found that the determination that Hovione’s method was not obvious at the time the patent was first issued was not changed by new prior art.

A competitor filed for inter parties reexamination in April 2005 based on prior art which was not considered during the prosecution of the patent. The reexamination examiner used that new art to find the patent claims were obvious and should be cancelled. When the examiner could not be persuaded to change that viewpoint, Dickstein Shapiro appealed on behalf of Hovione. An oral argument, at which the competitor also presented arguments, was held in September 2010.

The patented method involves complex steroid chemistry—an area in which Hovione has led since the 1960s—and a primary issue on the appeal was whether a particular compound was inherently formed in the course of performing the same process as previously as the result of using a stereoisomer of the compound used by the art in one step. A stereoisomer is a compound which is identical to another compound except that one group in the molecule has a different orientation in space when the three dimensional configuration is considered. The examiner advanced several scientific reasons to show Hovione’s compound was inherently produced, and the firm countered with several scientific arguments that the examiner was wrong, including statements made by the competitor in its own patent which it had not brought to the attention of the U.S. Patent Office.

The appeals board accepted all of the firm’s arguments, found that inherency had not been established, and rejected the arguments advanced by the examiner and the competitor.

Guy Villax, Hovione Chief Executive, commented as follows, “This outcome is a victory. One of the authors of this patent was Ivan Villax, my father and founder of Hovione—so we’d fight this one in any case. Fluticasone is a product where we believe we will continue to have a central role going forward. Our company believes in picking winners and not letting go.”

Dickstein Shapiro’s nationally ranked Intellectual Property Practice has more than 80 attorneys who work with clients to develop strategies that capitalize on their intellectual property assets and achieve their business objectives. The firm is ranked by Chambers USA, Managing Intellectual Property and Intellectual Property Today magazines as a top firm for intellectual property work. Dickstein Shapiro has the experience, skill, and knowledge to successfully solve intellectual property problems for clients striving to succeed in this ever-changing, highly competitive arena.

About Dickstein Shapiro LLP 

Dickstein Shapiro LLP, founded in 1953, is internationally recognized for its work with clients, from start-ups to Fortune 500 corporations. Dickstein Shapiro provides strategic counsel and develops multidisciplinary legal solutions by leveraging its core strengths—litigation, regulatory, transactions, and advocacy—to successfully advance clients’ business interests.

About Hovione 

Hovione is an international company with 51 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. 
For more information about Hovione, please visit the Hovione site at www.hovione.com  or contact Corporate Communications, Isabel Pina, + 351 21 982 9362, e-mail: ipina@hovione.com.

 

 

 

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Developing drugs with poor water solubility remains a major challenge for pharmaceutical manufacturers, because solubility impacts bioavailability and effective drug delivery. The vast majority of small molecule drug candidates have low water solubility. For more than two decades, the most successful particle engineering technology to improve drug solubility and bioavailability has been spray drying with an amorphous solid dispersion (ASD) platform. Spray drying improves the solubility of oral drugs, inhalable particles, and excipients, and increases the stability of heat-sensitive drug products. Hovione, recognized globally for its industry-leading spray drying capabilities, has recently completed a $100 million investment cycle to enhance its operations in New Jersey. This initiative has successfully doubled Hovione’s spray-drying capacity in the US, strengthening its position in the industry. Hovione’s Expanded U.S. Site in East Windsor, NJ  The first phase of the expansion in East Windsor, NJ, delivers a new 31,000 square foot facility and houses two size-3 spray dryers (PSD-3). This additional capacity allows Hovione to meet increasing customer demand for ASD development and good manufacturing practice (GMP) commercial production. GMP operations are scheduled to commence in the second quarter of 2026.  Hovione has also acquired 15 acres of neighboring land, strategically positioning itself for future growth and evolving customer needs for U.S. manufacturing. The newly acquired greenfield site will provide future support for PSD-4–scale commercial production as well as continuous and batch tableting production. It will also be a hub for centralized logistics, enhanced quality control laboratories, and next-generation research and development facilities.  A Global CDMO with a Growing U.S. Footprint  Hovione has operated in New Jersey for more than two decades, establishing itself with a strong U.S. presence for the production of drug substances, intermediates, and finished drug products. A continued emphasis on an integrated service offering, including spray drying, supports delivering innovative medicines to patients more quickly.  The expansion of the East Windsor site addresses the rising demand for U.S. manufacturing and is an integral part of the company's ongoing global growth strategy, with facilities in Portugal, Ireland, and Macau. The company continues to bolster a cohesive network for drug development and commercial manufacturing unified by a corporate quality system and governance framework.  The integrated offering enhances development speed and eases technology transfers by unifying the team's technical skills, proprietary technologies, and digital platforms to efficiently produce drug substance to drug products at a single-site, through Hovione’s “one site, one partner” vision. Furthermore, Hovione’s strategic partnership model offers customers exclusive access to advanced technologies and resources while aiding in the optimization of their development programs and ensuring sustained value creation.  End-to-End Spray Drying and Particle Engineering: From Grams to Tons Hovione is a global leader in spray drying and particle engineering. Services included solubility enhancement and controlled-modified release via development and production of ASDs of both small and large molecules, supporting various modalities. ASD-HIPROS, Hovione’s proprietary spray drying screening platform, identifies optimal formulations that offer optimal performance and stability. By increasing production volume in the US, Hovione will meet customer demand for spray drying services:  Development services in the laboratory (1 g – 1 kg batches)  Pilot scale production (0.5 – 25 kg batches)  Small-scale production (5 – 200 kg batches)  Large-scale commercial manufacturing (50 – 300 kg batches) A Commitment to Sustainability  Hovione’s core values include a commitment to sustainability at all facilities. This commitment is reflected in a business strategy that focuses on improving the communities where the company operates. Hovione’s sustainability policy and strategy align with the UN Sustainable Development Goals and include adherence to science-based targets in line with the Paris Agreement to address climate change. Meeting these goals has required a dedication to process intensification and ensuring sustainability of manufacturing processes. This has been possible through strategic planning and commitments from senior management to ensure sustainability is addressed throughout the drug development life cycle.  Partner with a Technology-Leading CDMO for U.S. Manufacturing   As demand for poorly water-soluble drug formulations continues to rise in the U.S., expanding spray drying throughput is essential to meet the need for innovative therapeutics. With proven leadership in spray drying to manufacture ASDs, Hovione is able to support pharmaceutical companies by solving their solubility challenges efficiently and reliably.  Partnering with a CDMO that combines global leadership, advanced technologies, and the necessary manufacturing capacity in the U.S., drug developers can expedite time to market, ensure quality, and deliver innovative medicines to patients faster.  If your company is seeking access to the latest spray-drying capabilities, expanded U.S. manufacturing capacity, and an accelerated path to regulatory filing and commercialization, contact our team today.     

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Hovione is Expanding Spray Drying Capacity for U.S. Drug Manufacturing

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Aim to accelerate drug development and production with new technologies. By: Charlie Sternberg Hovione, an international integrated pharmaceutical development and manufacturing organization, and Microinnova Engineering, a leader in continuous process intensification, have partnered to advance the development of multi-purpose, plug-and-play modular equipment for flow chemistry. The companies will work together to test Microinnova’s modular manufacturing equipment, which is designed to offer greater flexibility, easier scalability, enhanced efficiency, and sustainable practices in active ingredient production, in an industrial setting. Together, the companies aim to accelerate process development, facilitate a seamless transition from lab to large-scale manufacturing, and ultimately reduce the time to market for pharmaceutical customers. “This collaboration with Microinnova underscores Hovione’s commitment to innovation in pharmaceutical manufacturing, with flow chemistry playing an important role in our long-term drug substance strategy,” said Dr. Jean-Luc Herbeaux, CEO of Hovione. “This partnership will allow us to shape and validate emerging continuous manufacturing technologies, which can potentially accelerate drug development and production.” Dr. Dirk Kirschneck, Founder and Strategic Director at Microinnova, added, “This partnership reflects our shared vision to deliver modular manufacturing technologies that support pharmaceutical innovation and manufacturing excellence. We are proud to join forces with Hovione to showcase the capabilities of our next-generation modular equipment in a dynamic CDMO environment, demonstrating its versatility for multi-purpose manufacturing.”   Read the full article on ContractPharma.com  

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