Last Updated: November 8, 2026

Incyte Corp Company Profile

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What is the competitive landscape for INCYTE CORP

INCYTE CORP has four approved drugs.

There are forty-one US patents protecting INCYTE CORP drugs.

Drugs and US Patents for Incyte Corp

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Incyte Corp JAKAFI XR ruxolitinib phosphate TABLET, EXTENDED RELEASE;ORAL 217180-002 May 1, 2026 RX Yes No 9,206,187 ⤷  Start Trial ⤷  Start Trial
Incyte Corp JAKAFI XR ruxolitinib phosphate TABLET, EXTENDED RELEASE;ORAL 217180-003 May 1, 2026 RX Yes No 11,576,864*PED ⤷  Start Trial Y ⤷  Start Trial
Incyte Corp JAKAFI XR ruxolitinib phosphate TABLET, EXTENDED RELEASE;ORAL 217180-001 May 1, 2026 RX Yes No 9,814,722 ⤷  Start Trial ⤷  Start Trial
Incyte Corp OPZELURA ruxolitinib phosphate CREAM;TOPICAL 215309-001 Sep 21, 2021 RX Yes Yes 9,974,790*PED ⤷  Start Trial Y ⤷  Start Trial
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Exclusivity Expiration
Paragraph IV (Patent) Challenges for INCYTE CORP drugs
Drugname Dosage Strength Tradename Submissiondate
➤ Subscribe Tablets 5 mg, 10 mg, 15 mg, 20 mg, and 25 mg ➤ Subscribe 2015-12-17

Supplementary Protection Certificates for Incyte Corp Drugs

Patent Number Supplementary Protection Certificate SPC Country SPC Expiration SPC Description
2861595 PA2021519 Lithuania ⤷  Start Trial PRODUCT NAME: PEMIGATINIBAS ARBA JO FARMACISKAI PRIIMTINA DRUSKA; REGISTRATION NO/DATE: EU/1/21/1535 20210326
2455382 CR 2017 00018 Denmark ⤷  Start Trial PRODUCT NAME: RUXOLITINIB ELLER ET FARMACEUTISK ACCEPTABELT SALT DERAF, HERUNDER RUXOLITINIB FOSFAT; REG. NO/DATE: EU/1/12/773/001-016/C(2015)1740 20150313
2455382 201740011 Slovenia ⤷  Start Trial PRODUCT NAME: RUXOLITINIB OR PHARMACEUTICALLY ACCEPTABLE SALT THEREOF; NATIONAL AUTHORISATION NUMBER: EU/1/12/773/001-016; DATE OF NATIONAL AUTHORISATION: 20150311; AUTHORITY FOR NATIONAL AUTHORISATION: EU
1966202 PA2013002,C1966202 Lithuania ⤷  Start Trial PRODUCT NAME: RUXOLITINIBUM; REGISTRATION NO/DATE: EU/1/12/773/001-EU/1/12/773/003, 2 00120823
>Patent Number >Supplementary Protection Certificate >SPC Country >SPC Expiration >SPC Description
Similar Applicant Names
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Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.