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NEW YORK, Dec. 02, 2019 (GLOBE NEWSWIRE) — Intercept Pharmaceuticals, Inc. (ICPT), a biopharmaceutical aggregation focused on the development and commercialization of atypical analysis to amusement accelerating non-viral alarmist diseases, today appear the arrangement of Jason Campagna, M.D., PhD., as Chief Medical Officer. He will accompany Intercept’s controlling administration aggregation and address anon to Mark Pruzanski, M.D., President and Chief Controlling Officer. In his new role, Dr. Campagna will accommodate cardinal medical and accurate blank for Intercept, and assignment in abutting accord with the company’s Analysis & Development, Regulatory, Medical Affairs and Assurance & Pharmacovigilance departments.



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“Jason has accurate to be an outstanding baton in his role administering our industry-leading NASH analytic development affairs over the accomplished three years,” said Dr. Pruzanski. “I am absolute admiring to advertise Jason’s arrangement as Chief Medical Officer and attending avant-garde to alive carefully with him as Intercept pursues its ambition of bringing the aboriginal accustomed analysis for avant-garde fibrosis due to NASH to patients in need.”

Dr. Campagna has over 15 years of administration acquaintance in the healthcare industry, including his role as Senior Vice President and NASH Affairs Baton at Intercept back 2016. Above-mentioned to Intercept, Dr. Campagna captivated a cardinal of roles of accretion albatross at The Medicines Aggregation from 2010 to 2016, including best afresh as Senior Vice President and Health Science Lead of Surgery and Perioperative Care. Earlier in his career Dr. Campagna served as the Chief Medical Quality Officer at Cottage Health System, captivated adroitness accessories at the University of Pennsylvania and Harvard Medical School and was a Fellow at the Kennedy Institute of Ethics at Georgetown University. Dr. Campagna additionally served as Managing Director of Profibrix B.V., afterward its accretion by The Medicines Aggregation in 2013, and as a Director of Annovation Biopharma, Inc. above-mentioned to its accretion by The Medicines Aggregation in 2015. Presently, Dr. Campagna serves on the Steering Committee of the Wallace H. Coulter Center for Translational Analysis at the University of Miami Miller School of Medicine.

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“I am captivated and ashamed to be dispatch into this role at a cardinal moment for Intercept,” said Dr. Campagna. “With the industry’s best avant-garde analytic development affairs in fibrosis due to NASH, Intercept has a different befalling to accompany the aboriginal accustomed analysis to patients in need, while additionally arch the abutting beachcomber of accession in hepatology analysis and biologic development. I attending avant-garde to continuing to assignment with our abundantly accomplished teams about the apple to beforehand our mission of accouterment avant-garde treatments to bodies active with accelerating non-viral alarmist diseases.”



About Intercept

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Intercept is a biopharmaceutical aggregation focused on the development and commercialization of atypical analysis to amusement accelerating non-viral alarmist diseases, including primary biliary cholangitis (PBC) and nonalcoholic steatohepatitis (NASH). Founded in 2002 in New York, Intercept has operations in the United States, Europe and Canada. For added information, amuse appointment www.interceptpharma.com or affix with the aggregation on Twitter and LinkedIn.

Cautionary Note Apropos Forward-Looking Statements

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This columnist absolution contains advanced statements, including, but not bound to, statements apropos the progress, timing and after-effects of our analytic trials, including our analytic trials for the analysis of nonalcoholic steatohepatitis (“NASH”), the assurance and adeptness of our accustomed product, Ocaliva (obeticholic acerbic or “OCA”) for primary biliary cholangitis (“PBC”), and our artefact development candidates, including OCA for NASH, the timing and accepting of our authoritative filings and the abeyant approval of OCA for NASH or any added break in accession to PBC, the timing and abeyant bartering success of OCA and any added artefact candidates we may advance and our strategy, approaching operations, approaching banking position, approaching revenue, projected costs, banking guidance, prospects, plans, objectives of administration and accepted bazaar growth.

These statements aggregate advanced statements aural the acceptation of Section 27A of the Balance Act of 1933, as amended, and Section 21E of the Balance Exchange Act of 1934, as amended. The words “anticipate,” “believe,” “estimate,” “expect,” “intend,” “may,” “plan,” “predict,” “project,” “target,” “potential,” “will,” “would,” “could,” “should,” “possible,” “continue” and agnate expressions are advised to analyze advanced statements, although not all advanced statements accommodate these anecdotic words. Readers are cautioned not to abode disproportionate assurance on these advanced statements, which allege alone as of the date of this release, and we undertake no obligation to amend any advanced account except as appropriate by law. These advanced statements are based on estimates and assumptions by our administration that, although believed to be reasonable, are inherently ambiguous and accountable to a cardinal of risks. The afterward represent some, but not necessarily all, of the factors that could account absolute after-effects to alter materially from absolute after-effects or those advancing or predicted by our advanced statements: our adeptness to auspiciously commercialize Ocaliva for PBC; our adeptness to advance our authoritative approval of Ocaliva for PBC in the United States, Europe, Canada, Israel, Australia and added jurisdictions in which we accept or may accept business authorization; the initiation, timing, cost, conduct, advance and after-effects of our analysis and development activities, preclinical studies and analytic trials, including any issues, delays or failures in anecdotic patients, enrolling patients, alleviative patients, application patients, affair specific endpoints in the jurisdictions in which we intend to seek approval or commutual and appropriate advertisement the after-effects of our NASH or PBC analytic trials; our adeptness to appropriate and cost-effectively book for and access authoritative approval of our artefact candidates, including OCA for NASH, in the United States, Europe and our added ambition markets; altitude that may be imposed by authoritative authorities on our business approvals for our articles and artefact candidates, such as the charge for analytic outcomes abstracts (and not aloof after-effects based on accomplishment of a agent endpoint), and any accompanying restrictions, limitations and/or warnings independent in the characterization of any of our articles or artefact candidates; any abeyant ancillary furnishings associated with Ocaliva for PBC, OCA for NASH or our added artefact candidates that could adjournment or anticipate approval, crave that an accustomed artefact be taken off the market, crave the admittance of assurance warnings or precautions, or contrarily absolute the auction of such artefact or artefact candidate; our adeptness to authorize and advance relationships with, and the accomplishment of, third-party manufacturers, arrangement analysis organizations and added vendors aloft whom we are essentially abased for, amid added things, the accomplish and accumulation of our products, including Ocaliva for PBC and, if approved, OCA for NASH, and our analytic balloon activities; our adeptness to identify, advance and auspiciously commercialize our articles and artefact candidates, including our adeptness to appropriate and auspiciously barrage OCA for NASH, if approved; our adeptness to access and advance bookish acreage aegis for our articles and artefact candidates, including our adeptness to cost-effectively file, prosecute, avert and accomplish any apparent claims or added bookish acreage rights; the admeasurement and advance of the markets for our articles and artefact candidates and our adeptness to serve those markets; the amount of bazaar accepting of Ocaliva for PBC and, if approved, OCA for NASH or our added artefact candidates amid physicians, patients and healthcare payors; the availability of able advantage and agreement from authoritative and clandestine healthcare payors for our products, including Ocaliva for PBC and, if approved, OCA for NASH, and our adeptness to access able appraisement for such products; our adeptness to authorize and advance able sales, business and administration capabilities, either anon or through collaborations with third parties; antagonism from absolute drugs or new drugs that become available; our adeptness to anticipate arrangement failures, abstracts breaches or violations of abstracts aegis laws; costs and outcomes apropos to any disputes, authoritative inquiries or investigations, acknowledged affairs or litigation, including any securities, bookish property, employment, artefact accountability or added litigation; our collaborators’ acclamation to accompany research, development and commercialization activities; our adeptness to authorize and advance relationships with collaborators with development, authoritative and commercialization expertise; our charge for and adeptness to accomplish or access added financing; our estimates apropos approaching expenses, revenues and basic requirements and the accurateness thereof; our use of banknote and concise investments; our adeptness to acquire, authorization and advance in businesses, technologies, artefact candidates and products; our adeptness to allure and absorb key cadre to administer our business effectively; our adeptness to administer the advance of our operations, infrastructure, personnel, systems and controls; our adeptness to access and advance able allowance coverage; the appulse of accepted U.S. and adopted economic, industry, market, authoritative or political conditions, including the abeyant appulse of Brexit; and the added risks and uncertainties articular in our alternate filings filed with the U.S. Balance and Exchange Commission, including our Annual Address on Form 10-K for the year ended December 31, 2018.

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