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Last Updated: May 20, 2024

LUMASIRAN SODIUM - Generic Drug Details


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What are the generic sources for lumasiran sodium and what is the scope of patent protection?

Lumasiran sodium is the generic ingredient in one branded drug marketed by Alnylam Pharms Inc and is included in one NDA. There are fourteen patents protecting this compound. Additional information is available in the individual branded drug profile pages.

Lumasiran sodium has one hundred and sixty-nine patent family members in forty-two countries.

One supplier is listed for this compound.

Summary for LUMASIRAN SODIUM
International Patents:169
US Patents:14
Tradenames:1
Applicants:1
NDAs:1
Finished Product Suppliers / Packagers: 1
DailyMed Link:LUMASIRAN SODIUM at DailyMed
DrugPatentWatch® Estimated Loss of Exclusivity (LOE) Date for LUMASIRAN SODIUM
Generic Entry Date for LUMASIRAN SODIUM*:
Constraining patent/regulatory exclusivity:
Dosage:
SOLUTION;SUBCUTANEOUS

*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 LUMASIRAN SODIUM

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Alnylam Pharms Inc OXLUMO lumasiran sodium SOLUTION;SUBCUTANEOUS 214103-001 Nov 23, 2020 RX Yes Yes ⤷  Try a Trial ⤷  Try a Trial Y Y ⤷  Try a Trial
Alnylam Pharms Inc OXLUMO lumasiran sodium SOLUTION;SUBCUTANEOUS 214103-001 Nov 23, 2020 RX Yes Yes ⤷  Try a Trial ⤷  Try a Trial Y Y ⤷  Try a Trial
Alnylam Pharms Inc OXLUMO lumasiran sodium SOLUTION;SUBCUTANEOUS 214103-001 Nov 23, 2020 RX Yes Yes ⤷  Try a Trial ⤷  Try a Trial Y Y ⤷  Try a Trial
Alnylam Pharms Inc OXLUMO lumasiran sodium SOLUTION;SUBCUTANEOUS 214103-001 Nov 23, 2020 RX Yes Yes ⤷  Try a Trial ⤷  Try a Trial Y Y ⤷  Try a Trial
Alnylam Pharms Inc OXLUMO lumasiran sodium SOLUTION;SUBCUTANEOUS 214103-001 Nov 23, 2020 RX Yes Yes ⤷  Try a Trial ⤷  Try a Trial Y Y ⤷  Try a Trial
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Exclusivity Expiration

International Patents for LUMASIRAN SODIUM

Country Patent Number Title Estimated Expiration
Australia 2008340355 Targeting lipids ⤷  Try a Trial
Japan 2011505426 ⤷  Try a Trial
South Korea 20230113654 HAO1유전자 발현 억제용 조성물 및 방법 (HAO1 1 COMPOSITIONS AND METHODS FOR INHIBITION OF HAO1HYDROXYACID OXIDASE 1GLYCOLATE OXIDASE GENE EXPRESSION) ⤷  Try a Trial
Australia 2021269372 Compositions and methods for inhibition of hao1 (hydroxyacid oxidase 1 (glycolate oxidase)) gene expression ⤷  Try a Trial
Japan 6886818 ⤷  Try a Trial
>Country >Patent Number >Title >Estimated Expiration

Supplementary Protection Certificates for LUMASIRAN SODIUM

Patent Number Supplementary Protection Certificate SPC Country SPC Expiration SPC Description
3204015 2290011-2 Sweden ⤷  Try a Trial PRODUCT NAME: LUMASIRAN, OPTIONALLY IN THE FORM OF A SALT; REG. NO/DATE: EU/1/20/1496 20201123
3581654 301132 Netherlands ⤷  Try a Trial PRODUCT NAME: LUMASIRAN; REGISTRATION NO/DATE: EU/1/20/1496 20201123
3204015 2022C/509 Belgium ⤷  Try a Trial PRODUCT NAME: LUMASIRAN, INCLUSIEF ZOUTEN ERVAN; AUTHORISATION NUMBER AND DATE: EU/1/20/1496 20201123
3581654 C202130048 Spain ⤷  Try a Trial PRODUCT NAME: LUMASIRAN; NATIONAL AUTHORISATION NUMBER: EU/1/20/1496; DATE OF AUTHORISATION: 20201119; NUMBER OF FIRST AUTHORISATION IN EUROPEAN ECONOMIC AREA (EEA): EU/1/20/1496; DATE OF FIRST AUTHORISATION IN EEA: 20201119
3581654 LUC00218 Luxembourg ⤷  Try a Trial PRODUCT NAME: LUMASIRAN; AUTHORISATION NUMBER AND DATE: EU/1/20/1496 20201123
>Patent Number >Supplementary Protection Certificate >SPC Country >SPC Expiration >SPC Description

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