Gamifant Purple Book BLA 761107

BLA number
761107
Proprietary names
Gamifant
Proper names
emapalumab-lzsg
Applicant
Swedish Orphan Biovitrum AB (publ)
Center
CDER
First observed release
2020-05-01
Latest observed release
2026-06-01
Newest archive release
2026-06-01
FDA patent list
No patents listed in the captured FDA patent list; source updated 2025-06-11
Coverage
Present in newest release

Latest Known Product Presentations#

Product, Proprietary name, Proper name table
ProductProprietary nameProper nameLicense typeStrengthDosage formRoutePresentationMarketingLicensureApprovalPatent list provided
001Gamifantemapalumab-lzsg351(a)10MG/2ML (5MG/ML)InjectionIntravenousSingle-Dose VialRxLicensed2018-11-20
002Gamifantemapalumab-lzsg351(a)50MG/10ML (5MG/ML)InjectionIntravenousSingle-Dose VialRxLicensed2018-11-20
003Gamifantemapalumab-lzsg351(a)100MG/20ML (5MG/ML)InjectionIntravenousSingle-Dose VialRxLicensed2020-06-26
004Gamifantemapalumab-lzsg351(a)50MG/2ML (25MG/ML)InjectionIntravenousSingle-Dose VialRxLicensed2023-06-07
005Gamifantemapalumab-lzsg351(a)100MG/4ML (25MG/ML)InjectionIntravenousSingle-Dose VialRxLicensed2023-06-07
006Gamifantemapalumab-lzsg351(a)250MG/10ML (25MG/ML)InjectionIntravenousSingle-Dose VialRxLicensed2023-06-07

Published Patent List#

No patents for this BLA were listed in the FDA Purple Book patent list captured from the source updated 2025-06-11.

Official Monthly Change Events#

Release, Event, Product table
ReleaseEventProductNameLicense typeStatusApplicant
2025-07-01N004Gamifant351(a)RxSwedish Orphan Biovitrum AB (publ)
2025-07-01N005Gamifant351(a)RxSwedish Orphan Biovitrum AB (publ)
2025-07-01N006Gamifant351(a)RxSwedish Orphan Biovitrum AB (publ)
2020-08-01U001Gamifant351(a)RxSwedish Orphan Biovitrum AB (publ)
2020-08-01U002Gamifant351(a)RxSwedish Orphan Biovitrum AB (publ)
2020-08-01N003Gamifant351(a)RxSwedish Orphan Biovitrum AB (publ)
2020-05-01R001Gamifant351(a)RxNovimmune SA
2020-05-01R002Gamifant351(a)RxNovimmune SA

Observed Product State History#

Release, Product, Name table
ReleaseProductNameLicense typeMarketingLicensureApproval
2025-07-01004Gamifant351(a)RxLicensed2023-06-07
2025-07-01005Gamifant351(a)RxLicensed2023-06-07
2025-07-01006Gamifant351(a)RxLicensed2023-06-07
2020-08-01003Gamifant351(a)RxLicensed2020-06-26
2020-05-01001Gamifant351(a)RxLicensed2018-11-20
2020-05-01002Gamifant351(a)RxLicensed2018-11-20