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Product profile · United States

LISRAYA

 ·  Patent Litigation & Settlement History ↓

IngredientBREPOCITINIB TOSYLATE
Application typeNDA
Application220106
Product001
Dosage formTABLET
RouteORAL
StrengthEQ 30MG BASE
Approval date2026-08-27
Marketing statusPrescription
Status event—
ApplicantPRIOVANT THERAP
Product source

Current GenericRadar decision

Year2035
SelectionDEEP_REVIEW
ReviewFINAL
Anchor typeTRUE_DS_PATENT
Anchor date2035-08-19
Patent anchor2035-08-19
Exclusivity anchor—
Protection date2043-07-30
First Final ANDA—
Status event—

POST_ANCHOR_TAIL: Issued claim 1 expressly covers brepocitinib tosylate Form A by XRPD peaks. It is a target-salt FTO tail, not an unrestricted TRUE_DS claim. Public adjusted date is recorded; even its 2041-06-08 unadjusted term exceeds the 2035 anchor. US12312358 free-base crystal is kept separate from target-salt coverage.

Patent estate

PatentEffective dateOfficial listingTRUE_DSDS gradeClaim classification / basisPTEPEDFamily
US111978672035-08-19CLAIM_REVIEW_NOT_EXACT_OB_LISTING —YNTRUE_DS
Brepocitinib chemical identity matches the compound claims. Original nonprovisional filing 2015-08-19 and zero PTA; later recovered compound grant US11197867 also has zero PTA. Psoriasis-only claims and fixed crystal claims are not full-scope anchors. New dermatomyositis applications remain applications, not issued rights.
———
US111978672035-08-19DS;DP ————
OB official listing only. TRUE_DS/DS-equivalent/claim scope/PTE-PED effective anchor remains unconfirmed.
———
US96635262035-08-19CLAIM_REVIEW_NOT_EXACT_OB_LISTING —YNTRUE_DS
Brepocitinib chemical identity matches the compound claims. Original nonprovisional filing 2015-08-19 and zero PTA; later recovered compound grant US11197867 also has zero PTA. Psoriasis-only claims and fixed crystal claims are not full-scope anchors. New dermatomyositis applications remain applications, not issued rights.
———
US96635262035-08-19DS;DP ————
OB official listing only. TRUE_DS/DS-equivalent/claim scope/PTE-PED effective anchor remains unconfirmed.
———
US126739552043-07-30CLAIM_REVIEW_NOT_EXACT_OB_LISTING —NNOTHER_CRYSTAL
Issued claim 1 expressly covers brepocitinib tosylate Form A by XRPD peaks. It is a target-salt FTO tail, not an unrestricted TRUE_DS claim. Public adjusted date is recorded; even its 2041-06-08 unadjusted term exceeds the 2035 anchor. US12312358 free-base crystal is kept separate from target-salt coverage.
———

Regulatory exclusivity

CodeStart dateEnd dateScopeEntire productAll indicationsFull coverage dateCombinationSource
NCE—2031-08-27————Source

2026-10-13 · NO_REGULATORY_EXCLUSIVITY_IDENTIFIED · Historical coverage: ANNUALS_AND_MONTHLY_REVIEWED

2026-10-10 · NO_RECORD_IN_CURRENT_SNAPSHOT · Historical coverage: NOT_COMPLETE

Generic approval evidence

Application / productEventFinal dateTentative dateApplicantAuthorized genericExact mappingSource
No generic approval facts are linked to this product.

Market Entry Information

API filings, authorized generics and linked regulatory milestones.

API Master Files & Certifications 0 records

Ingredient-level registrations from linked public manufacturer portfolios. A filing does not establish supply to this finished product. DMFs are not FDA approvals.

APIHolder / manufacturerHolder countryFiling typeNumberStatusFiled dateAvailable for referenceSourceLast verified
No master-file or certification records are linked through public manufacturer portfolios.

Authorized Generics 0 records

Authorized generics are shown separately from independent ANDA approvals.

Application / productApplicantEvent / status First marketed Product mappingSourceLast verified
No authorized-generic records are linked to this product.

Tentative ANDA Approvals 0 records

Tentative approval is not final approval. Historical tentative approvals remain visible after a linked final approval.

Application / productApplicantEvent / status Tentative date Follow-up final approvalProduct mappingSourceLast verified
No tentative-approval records are linked to this product.

Paragraph IV Challenges 0 records

Paragraph IV challenges below are sourced from legal records separately from FDA approvals. An ANDA filing, lawsuit or settlement does not establish final approval or commercial launch.

Application / productApplicantEvent / status Certification event date Product mappingSourceLast verified
No structured Paragraph IV certification events are linked in the available approval evidence.

Final ANDA Approvals 0 records

Approval dates do not establish commercial launch. Product mapping is shown for each linked record.

Application / productApplicantEvent / status Final approval date Product mappingSourceLast verified
No final-approval records are linked to this product.
Decision evidence (4)
TypeDateRoleBasisSource
PATENT2035-08-19CANONICAL_ANCHORBrepocitinib chemical identity matches the compound claims. Original nonprovisional filing 2015-08-19 and zero PTA; later recovered compound grant US11197867 also has zero PTA. Psoriasis-only claims and fixed crystal claims are not full-scope anchors. New dermatomyositis applications remain applications, not issued rights.Source
PATENT2035-08-19CANONICAL_ANCHORBrepocitinib chemical identity matches the compound claims. Original nonprovisional filing 2015-08-19 and zero PTA; later recovered compound grant US11197867 also has zero PTA. Psoriasis-only claims and fixed crystal claims are not full-scope anchors. New dermatomyositis applications remain applications, not issued rights.Source
PATENT2043-07-30FTO_TAILIssued claim 1 expressly covers brepocitinib tosylate Form A by XRPD peaks. It is a target-salt FTO tail, not an unrestricted TRUE_DS claim. Public adjusted date is recorded; even its 2041-06-08 unadjusted term exceeds the 2035 anchor. US12312358 free-base crystal is kept separate from target-salt coverage.Source
REGULATORY_STATUS2035-08-19CANONICAL_DECISIONPOST_ANCHOR_TAIL: Issued claim 1 expressly covers brepocitinib tosylate Form A by XRPD peaks. It is a target-salt FTO tail, not an unrestricted TRUE_DS claim. Public adjusted date is recorded; even its 2041-06-08 unadjusted term exceeds the 2035 anchor. US12312358 free-base crystal is kept separate from target-salt coverage.Source
Independent legal-event information

Litigation & Settlement History

Settlement launch rights generally apply only to the named parties and product scope. These records do not change GenericRadar patent/exclusivity anchors or current decisions.

No litigation or settlement record currently linked to this product.