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Product profile · United States

BIXLENVO

 ·  Patent Litigation & Settlement History ↓

IngredientBICTEGRAVIR SODIUM; LENACAPAVIR SODIUM
Application typeNDA
Application221104
Product001
Dosage formTABLET
RouteORAL
StrengthEQ 75MG BASE;EQ 50MG BASE
Approval date2026-08-27
Marketing statusPrescription
Status event—
ApplicantGILEAD SCIENCES INC
Product source

Current GenericRadar decision

Year2037
SelectionDEEP_REVIEW
ReviewFINAL
Anchor typeTRUE_DS_PATENT
Anchor date2037-08-17
Patent anchor2037-08-17
Exclusivity anchor—
Protection date2038-08-16
First Final ANDA—
Status event—

POST_ANCHOR_TAIL: Lenacapavir sodium crystalline Form I claims remain after the 2037 compound anchor. Crystal claims are retained for FTO without asserting that every commercial sample meets the XRPD limitations.

Patent estate

PatentEffective dateOfficial listingTRUE_DSDS gradeClaim classification / basisPTEPEDFamily
92169962033-12-19CLAIM_REVIEW_NOT_EXACT_OB_LISTING —YNTRUE_DS
Bictegravir component compound end precedes the selected lenacapavir anchor.
———
92169962033-12-19DS;DP ————
OB official listing only. TRUE_DS/DS-equivalent/claim scope/PTE-PED effective anchor remains unconfirmed.
———
97320922033-12-19CLAIM_REVIEW_NOT_EXACT_OB_LISTING —YNTRUE_DS
Bictegravir component compound end precedes the selected lenacapavir anchor.
———
97320922033-12-19DS;DP ————
OB official listing only. TRUE_DS/DS-equivalent/claim scope/PTE-PED effective anchor remains unconfirmed.
———
99510432034-02-28DS;DP;U U-4602———
OB official listing only. TRUE_DS/DS-equivalent/claim scope/PTE-PED effective anchor remains unconfirmed.
———
103850672035-06-19U U-4602———
OB official listing only. TRUE_DS/DS-equivalent/claim scope/PTE-PED effective anchor remains unconfirmed.
———
97083422035-06-19DS;DP ————
OB official listing only. TRUE_DS/DS-equivalent/claim scope/PTE-PED effective anchor remains unconfirmed.
———
100719852037-08-17CLAIM_REVIEW_NOT_EXACT_OB_LISTING —YNTRUE_DS
Lenacapavir unrestricted compound claim supplies the later component anchor. Bictegravir compound ends 2033-12-19. Sodium salt/crystal claims are not promoted automatically. Injectable-only claims and BIC/TAF/FTC tablet claims do not establish a two-component oral anchor. Active-moiety NCE ends 2027-12-22 and is earlier.
———
100719852037-08-17DS;DP ————
OB official listing only. TRUE_DS/DS-equivalent/claim scope/PTE-PED effective anchor remains unconfirmed.
———
106548272037-08-17U U-4602———
OB official listing only. TRUE_DS/DS-equivalent/claim scope/PTE-PED effective anchor remains unconfirmed.
———
112677992038-08-16CLAIM_REVIEW_NOT_EXACT_OB_LISTING —NNOTHER_CRYSTAL
Lenacapavir sodium crystalline Form I claims remain after the 2037 compound anchor. Crystal claims are retained for FTO without asserting that every commercial sample meets the XRPD limitations.
———
112677992038-08-16DS ————
OB official listing only. TRUE_DS/DS-equivalent/claim scope/PTE-PED effective anchor remains unconfirmed.
———

Regulatory exclusivity

CodeStart dateEnd dateScopeEntire productAll indicationsFull coverage dateCombinationSource
NCE—2027-12-22————Source
NP—2029-08-27————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 (5)
TypeDateRoleBasisSource
PATENT2033-12-19HISTORICAL_CONTEXTBictegravir component compound end precedes the selected lenacapavir anchor.Source
PATENT2033-12-19HISTORICAL_CONTEXTBictegravir component compound end precedes the selected lenacapavir anchor.Source
PATENT2037-08-17CANONICAL_ANCHORLenacapavir unrestricted compound claim supplies the later component anchor. Bictegravir compound ends 2033-12-19. Sodium salt/crystal claims are not promoted automatically. Injectable-only claims and BIC/TAF/FTC tablet claims do not establish a two-component oral anchor. Active-moiety NCE ends 2027-12-22 and is earlier.Source
PATENT2038-08-16FTO_TAILLenacapavir sodium crystalline Form I claims remain after the 2037 compound anchor. Crystal claims are retained for FTO without asserting that every commercial sample meets the XRPD limitations.Source
REGULATORY_STATUS2037-08-17CANONICAL_DECISIONPOST_ANCHOR_TAIL: Lenacapavir sodium crystalline Form I claims remain after the 2037 compound anchor. Crystal claims are retained for FTO without asserting that every commercial sample meets the XRPD limitations.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.