Market LIVE
Published markets; coverage varies by country
Product profile · United States

TRYNGOLZA (AUTOINJECTOR)

 ·  Patent Litigation & Settlement History ↓

IngredientOLEZARSEN SODIUM
Application typeNDA
Application218614
Product001
Dosage formSOLUTION
RouteSUBCUTANEOUS
StrengthEQ 80MG BASE/0.8ML (EQ 80MG BASE/0.8ML)
Approval date2024-12-19
Marketing statusPrescription
Status event—
ApplicantIONIS PHARMS INC
Product source

Current GenericRadar decision

Year2034
SelectionCANDIDATE
ReviewFINAL
Anchor typeTRUE_DS_PATENT
Anchor date2034-05-01
Patent anchor2034-05-01
Exclusivity anchor—
Protection date2034-05-01
First Final ANDA—
Status event—

US9163239 corrected c23/24; olezarsen sequence/GalNAc/MOE/PS compared;50/80mg separate.

Patent estate

PatentEffective dateOfficial listingTRUE_DSDS gradeClaim classification / basisPTEPEDFamily
91570822032-04-27U U-4050NYDS_EQUIVALENT
———
91570822032-04-27U U-4580NYDS_EQUIVALENT
———
95933332034-02-14U U-4050NNU
———
125096842034-05-01U U-4050NYDS_EQUIVALENT
———
125096842034-05-01U U-4580NYDS_EQUIVALENT
———
91272762034-05-01DS —YNTRUE_DS
———
91632392034-05-01DS —YNTRUE_DS
———
91815492034-05-01DS —YNTRUE_DS
———

Regulatory exclusivity

CodeStart dateEnd dateScopeEntire productAll indicationsFull coverage dateCombinationSource
I-992—2029-06-24————Source
ODE-515—2031-12-19————Source

2026-10-10 · CURRENT_SOURCE_RECORDS_FOUND · 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 (1)
TypeDateRoleBasisSource
ANNUAL_DECISION_RECHECK—ANCHOR_AND_TAILUS9163239 corrected c23/24; olezarsen sequence/GalNAc/MOE/PS compared;50/80mg separate.Source
Decision history
CurrentYearStatusReviewAnchorJudged
Y2034CANDIDATEFINAL2034-05-012026-10-17 20:32:21
N2034CANDIDATEFINAL2034-05-012026-10-15 23:00:04
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.