ROCKVILLE, Md., June 13, 2017 -- Sucampo Pharmaceuticals, Inc. (Sucampo) (Nasdaq:SCMP), a global biopharmaceutical company, today announced that the U.S. Patent and Trademark Office has issued a patent for VTS-270, a novel and well-characterized 2-hydroxypropyl-beta-cyclodextrin (HPβCD) product, under investigation as an intrathecally administered treatment for Niemann-Pick Disease Type C1 (NPC-1).
The patent, U.S. Patent No. 9,675,634, relates to proprietary cyclodextrin compositions with a specific fingerprint and purity profile that distinguish VTS-270 from other HPβCD products. The patent expires in 2036.
“We’re very pleased with the issuance of this patent, which protects the differentiated composition of VTS-270 and strengthens our intellectual property position,” said Peter Greenleaf, Chairman and Chief Executive Officer, Sucampo Pharmaceuticals. “The patent is further evidence of the profile of VTS-270, which we believe may provide a much-needed treatment for patients and families living with NPC-1.”
VTS-270, which is currently in a pivotal Phase 2b/3 trial, has been granted breakthrough therapy designation in the U.S. and orphan designation in both the U.S. and EU. Results from the pivotal trial are expected in mid-2018. NPC-1 is a rare, progressive and ultimately lethal genetic disorder affecting an estimated 2,000-3,000 patients globally. Effective treatment of NPC remains a high unmet need, with no approved products for patients in the U.S.
About Sucampo Pharmaceuticals, Inc.
Sucampo Pharmaceuticals, Inc. is a biopharmaceutical company focused on the development and commercialization of highly specialized medicines. Sucampo has a late-stage pipeline of product candidates in clinical development for orphan disease areas, including VTS-270, a 2-hydroxypropyl-beta-cyclodextrin product with a specific compositional fingerprint that has been granted orphan designation in the U.S. and Europe and is in a pivotal Phase 2b/3 clinical trial for the treatment of Niemann-Pick Disease Type C-1, a rare progressive genetic disorder. VTS-270 also has been granted breakthrough therapy designation in the U.S. Sucampo has an exclusive option for the North American rights to CPP1-x/sulindac, which is in Phase 3 development for the treatment of familial adenomatous polyposis and has been granted orphan drug designation in the U.S. The company has two marketed products – AMITIZA and RESCULA. For more information, please visit www.sucampo.com.
The Sucampo logo and the tagline, The Science of Innovation, AMITIZA and RESCULA are registered trademarks of Sucampo and its affiliates.
Follow us on Twitter (@Sucampo_Pharma). Follow us on LinkedIn (Sucampo Pharmaceuticals).
Twitter LinkedIn
Contact Sucampo Pharmaceuticals, Inc. Silvia Taylor Senior Vice President, Investor Relations and Corporate Affairs 1-240-223-3718 [email protected]


Abbott Laboratories Ordered to Pay $53 Million in Premature Infant Formula Lawsuit
U.S. Automakers Push Back Against EU Rules Blocking American Trucks from European Market
FedEx Pilots and Union Reach Tentative Agreement on 40% Pay Increase
Anthropic Fights Pentagon Blacklisting in Dual Federal Court Battles
Bendigo and Adelaide Bank Posts Strong Q3 Earnings, Announces AI-Driven Job Cuts
Alibaba Shares Slide as Jefferies Slashes Price Target Over AI Spending and Business Losses
LG Electronics Posts Record Q1 Revenue Amid Strong Demand and Cost Improvements
Tokyo Electric Power Attracts Major Investors Amid Billion-Dollar Restructuring Push
Apple's Foldable iPhone Faces Engineering Setbacks, Mass Production Timeline at Risk
Chalco Stock Surges as Q1 2025 Profit Forecast Jumps Up to 58%
China's AI Stocks Surge as Zhipu and MiniMax Hit Record Highs
BHP's Incoming CEO Visits China Amid Pricing Dispute with CMRG
Disney Plans to Cut 1,000 Jobs Amid Ongoing Restructuring Efforts
Bank of America Identifies Top Asia-Pacific Semiconductor Stocks Poised for AI-Driven Growth
Goldman Sachs, ANZ Cut Oil Forecasts Amid U.S.-Iran Ceasefire Hopes
Bill Ackman Eyes New Fund to Bet Against Market Complacency 



