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Last Updated: May 23, 2024

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LYTGOBI Drug Patent Profile


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When do Lytgobi patents expire, and what generic alternatives are available?

Lytgobi is a drug marketed by Taiho Oncology and is included in one NDA. There are three patents protecting this drug.

This drug has sixty-nine patent family members in twenty-five countries.

The generic ingredient in LYTGOBI is futibatinib. One supplier is listed for this compound. Additional details are available on the futibatinib profile page.

DrugPatentWatch® Generic Entry Outlook for Lytgobi

Lytgobi will be eligible for patent challenges on September 30, 2026. This date may extended up to six months if a pediatric exclusivity extension is applied to the drug's patents.

By analyzing the patents and regulatory protections it appears that the earliest date for generic entry will be September 30, 2029. This may change due to patent challenges or generic licensing.

Indicators of Generic Entry

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Summary for LYTGOBI
International Patents:69
US Patents:3
Applicants:1
NDAs:1
Finished Product Suppliers / Packagers: 1
Raw Ingredient (Bulk) Api Vendors: 32
Patent Applications: 47
Drug Prices: Drug price information for LYTGOBI
What excipients (inactive ingredients) are in LYTGOBI?LYTGOBI excipients list
DailyMed Link:LYTGOBI at DailyMed
Drug patent expirations by year for LYTGOBI
Drug Prices for LYTGOBI

See drug prices for LYTGOBI

DrugPatentWatch® Estimated Loss of Exclusivity (LOE) Date for LYTGOBI
Generic Entry Date for LYTGOBI*:
Constraining patent/regulatory exclusivity:
TREATMENT OF ADULT PATIENTS WITH PREVIOUSLY TREATED, UNRESECTABLE, LOCALLY ADVANCED OR METASTATIC INTRAHEPATIC CHOLANGIOCARCINOMA HARBORING FIBROBLAST GROWTH FACTOR RECEPTOR 2 (FGFR2) GENE FUSIONS OR OTHER REARRANGEMENTS
NDA:
Dosage:
TABLET;ORAL

*The generic entry opportunity date is the latter of the last compound-claiming patent and the last regulatory exclusivity protection. Many factors can influence early or later generic entry. This date is provided as a rough estimate of generic entry potential and should not be used as an independent source.

US Patents and Regulatory Information for LYTGOBI

LYTGOBI is protected by three US patents and two FDA Regulatory Exclusivities.

Based on analysis by DrugPatentWatch, the earliest date for a generic version of LYTGOBI is ⤷  Sign Up.

This potential generic entry date is based on TREATMENT OF ADULT PATIENTS WITH PREVIOUSLY TREATED, UNRESECTABLE, LOCALLY ADVANCED OR METASTATIC INTRAHEPATIC CHOLANGIOCARCINOMA HARBORING FIBROBLAST GROWTH FACTOR RECEPTOR 2 (FGFR2) GENE FUSIONS OR OTHER REARRANGEMENTS.

Generics may enter earlier, or later, based on new patent filings, patent extensions, patent invalidation, early generic licensing, generic entry preferences, and other factors.

Patents protecting LYTGOBI


Patent Number: ⤷  Sign Up
Patent Expiration: ⤷  Sign Up


Patent Number: ⤷  Sign Up
Patent Expiration: ⤷  Sign Up


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Patent Expiration: ⤷  Sign Up
Patented Use: METHOD OF TREATING INTRAHEPATIC CHOLANGIOCARCINOMA

FDA Regulatory Exclusivity protecting LYTGOBI

NEW CHEMICAL ENTITY
Exclusivity Expiration: ⤷  Sign Up

TREATMENT OF ADULT PATIENTS WITH PREVIOUSLY TREATED, UNRESECTABLE, LOCALLY ADVANCED OR METASTATIC INTRAHEPATIC CHOLANGIOCARCINOMA HARBORING FIBROBLAST GROWTH FACTOR RECEPTOR 2 (FGFR2) GENE FUSIONS OR OTHER REARRANGEMENTS
Exclusivity Expiration: ⤷  Sign Up

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Taiho Oncology LYTGOBI futibatinib TABLET;ORAL 214801-001 Sep 30, 2022 RX Yes Yes ⤷  Sign Up ⤷  Sign Up Y Y ⤷  Sign Up
Taiho Oncology LYTGOBI futibatinib TABLET;ORAL 214801-001 Sep 30, 2022 RX Yes Yes ⤷  Sign Up ⤷  Sign Up ⤷  Sign Up
Taiho Oncology LYTGOBI futibatinib TABLET;ORAL 214801-001 Sep 30, 2022 RX Yes Yes ⤷  Sign Up ⤷  Sign Up Y ⤷  Sign Up
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Exclusivity Expiration

EU/EMA Drug Approvals for LYTGOBI

Company Drugname Inn Product Number / Indication Status Generic Biosimilar Orphan Marketing Authorisation Marketing Refusal
Taiho Pharma Netherlands B.V. Lytgobi futibatinib EMEA/H/C/005627
Lytgobi monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic cholangiocarcinoma with a fibroblast growth factor receptor 2 (FGFR2) fusion or rearrangement that have progressed after at least one prior line of systemic therapy.
Authorised no no no 2023-07-04
>Company >Drugname >Inn >Product Number / Indication >Status >Generic >Biosimilar >Orphan >Marketing Authorisation >Marketing Refusal

International Patents for LYTGOBI

See the table below for patents covering LYTGOBI around the world.

Country Patent Number Title Estimated Expiration
Russian Federation 2759746 ФАРМАЦЕВТИЧЕСКАЯ КОМПОЗИЦИЯ, ВКЛЮЧАЮЩАЯ АЛКИЛСУЛЬФАТ НАТРИЯ (PHARMACEUTICAL COMPOSITION INCLUDING SODIUM ALKYL SULPHATE) ⤷  Sign Up
South Korea 101917557 ⤷  Sign Up
Mexico 2017012568 CRISTAL DEL COMPUESTO ALQUINIL BENCENO 3,5-DISUSTITUIDO. (CRYSTAL OF 3,5-DISUBSTITUTED BENZENE ALKYNYL COMPOUND.) ⤷  Sign Up
>Country >Patent Number >Title >Estimated Expiration

Supplementary Protection Certificates for LYTGOBI

Patent Number Supplementary Protection Certificate SPC Country SPC Expiration SPC Description
2657233 CA 2023 00036 Denmark ⤷  Sign Up PRODUCT NAME: FUTIBATINIB ELLER ET SALT DERAF; REG. NO/DATE: EU/1/23/1741 20230706
2657233 2023C/548 Belgium ⤷  Sign Up PRODUCT NAME: FUTIBATINIB OF EEN ZOUT DAARVAN; AUTHORISATION NUMBER AND DATE: EU/1/23/1741 20230706
2657233 CR 2023 00036 Denmark ⤷  Sign Up PRODUCT NAME: FUTIBATINIB ELLER ET SALT DERAF; REG. NO/DATE: EU/1/23/1741 20230706
>Patent Number >Supplementary Protection Certificate >SPC Country >SPC Expiration >SPC Description

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