Organization, Consolidation and Presentation of Financial Statements Disclosure [Text Block] | 1. Description of the Business Sucampo Pharmaceuticals, Inc., (Company) is a global biopharmaceutical company focused on developing, identifying, acquiring and bringing to market innovative medicines that meet unmet medical needs. The Company’s primary focus areas are medicines that treat gastrointestinal, ophthalmic, neurological, and oncology disorders. The Company currently generates revenue mainly from product royalties, upfront and milestone payments, product sales and reimbursements for development activities. The Company expects to continue to incur significant expenses for the next several years as it continues its research and development activities, seeks additional regulatory approvals and additional indications for approved products and other compounds, and seeks strategic opportunities for acquiring new products and product candidates. AMITIZA ® three October 2014, April 2006, May 2008 May 2013. may October 2015, October 2014, December 2020. January 2021, The Company has also partnered with Par Pharmaceuticals, Inc. (Par) and Dr. Reddy’s Laboratories, Ltd. (Dr. Reddy’s) in connection with the settlement of patent litigation in the U.S. related to the Company’s AMITIZA 8 24 8 24 January 1, 2021, January 1, 2021, 8 24 not six November 9, 2016, In Japan, AMITIZA is marketed under a license, commercialization and supply agreement (the Japan Mylan Agreement) that was transferred to Mylan, Inc. (Mylan) from Abbott Laboratories, Inc. (Abbott), as of February 2015, June 2012 November 2012. not In May 2015, $1.0 June 2015, $500,000 $1.5 June 2015, $1.5 In October 2014, April 2015, 2016. Before the execution of the Global Takeda Agreement, the Company retained full rights to develop and commercialize AMITIZA for the rest of the world’s markets outside of the U.S., Canada and Japan. In the U.K., the Company received approval in September 2012 fourth 2013. July 2014, January 2015, In Switzerland, AMITIZA was approved to treat CIC in 2009. 2012, first 2013. February 2014, first two nine July 2014, October 2015, In October 2015, June 2015. December 2015, 3 March 2016 May 2016. June 2015, July 2016. December 2015. May 2016, June 2016, 2017 In the U.S., the Company ceased marketing RESCULA (unoprostone isopropyl), an ophthalmology product, in the fourth 2014 no March 2015 May 2015, October 2015, The Company’s clinical development programs include the following: Lubiprostone Alternate Formulation The Company has been developing an alternate formulation of lubiprostone for both adult and pediatric patients who are unable to take or tolerate capsules and for naso-gastric tube fed patients. Takeda has agreed to fund 100% 3 second 2016 second 2017. Lubiprostone for Pediatric Functional Constipation A Phase 3 four first two one 2016, 6 17 first 12 December 2013 April 2016. second March 2014. November 2016, 3 6 17 July 28, 2017. 3 2018 3 6 6 70% 50% CPP 1 In January 2016, 1X/sulindac 3 no 3 310, 150 three On June 7, 2017, no 3 310, 1X/sulindac 2018. $4.5 second July 2017, three six June 30, 2017. VTS- 270 C1 1 On March 31, 2017, 270, April 3, 2017. 270 2 270 may 1, 270, 2b/3 1 no 2018. The Company accounted for the transaction as an asset acquisition and incurred an acquired in-process research and development charge of $186.6 no second 2017. $13.6 Basis of Presentation The accompanying unaudited Condensed Consolidated Financial Statements have been prepared in accordance with generally accepted accounting principles in the United States of America (GAAP) and the rules and regulations of the U.S. Securities and Exchange Commission (SEC) for interim financial information. Accordingly, they do not December 31, 2016 10 March 8, 2017. June 30, 2017 three six June 30, 2017 2016 not not may The Condensed Consolidated Financial Statements include the accounts of the Company and its wholly-owned subsidiaries: Sucampo AG (SAG) and Sucampo Acquisitions GmbH (SAQ) based in Zug, Switzerland and Vtesse Europe Ltd., based in the United Kingdom, through which the Company conducts certain of its worldwide and European operations; Sucampo Pharma, LLC (SPL) based in Tokyo, Japan, through which the Company conducts its Asian operations, manufacturing and certain development operations; and Sucampo Pharma Americas LLC (SPA) and Vtesse Inc., based in Rockville, Maryland, through which the Company conducts its North American operations. All inter-company balances and transactions have been eliminated. The preparation of financial statements in conformity with GAAP requires management to make estimates that affect the reported amounts of assets and liabilities at the date of the financial statements, disclosure of contingent assets and liabilities, and the reported amounts of revenue and expenses during the reporting period. Actual results could differ from those estimates. |