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Last Updated: November 15, 2024

pomalyst Drug Patent Profile


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Which patents cover Pomalyst, and what generic alternatives are available?

Pomalyst is a drug marketed by Bristol and is included in one NDA. There are four patents protecting this drug and one Paragraph IV challenge.

This drug has three hundred and fifty-seven patent family members in forty-eight countries.

The generic ingredient in POMALYST is pomalidomide. There are eleven drug master file entries for this compound. One supplier is listed for this compound. Additional details are available on the pomalidomide profile page.

DrugPatentWatch® Litigation and Generic Entry Outlook for Pomalyst

A generic version of pomalyst was approved as pomalidomide by APOTEX on June 11th, 2024.

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Drug patent expirations by year for pomalyst
Drug Prices for pomalyst

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Recent Clinical Trials for pomalyst

Identify potential brand extensions & 505(b)(2) entrants

SponsorPhase
MegalabsPhase 1
University of ChicagoPhase 2
Regeneron PharmaceuticalsPhase 3

See all pomalyst clinical trials

Pharmacology for pomalyst
Drug ClassThalidomide Analog
Paragraph IV (Patent) Challenges for POMALYST
Tradename Dosage Ingredient Strength NDA ANDAs Submitted Submissiondate
POMALYST Capsules pomalidomide 1 mg, 2 mg, 3 mg and 4 mg 204026 6 2017-02-08

US Patents and Regulatory Information for pomalyst

pomalyst is protected by four US patents and five FDA Regulatory Exclusivities.

Patents protecting pomalyst

Formulations of 4-amino-2-(2,6-dioxopiperidine-3-yl)isoindoline-1,3-dione
Patent Number: ⤷  Sign Up
Patent Expiration: ⤷  Sign Up

Methods for treating multiple myeloma using 4-(amino)-2-(2,6-dioxo(3-piperidyl))-isoindoline-1,3-dione
Patent Number: ⤷  Sign Up
Patent Expiration: ⤷  Sign Up

Formulations of 4-amino-2-(2,6-dioxopiperidine-3-yl)isoindoline-1,3-dione
Patent Number: ⤷  Sign Up
Patent Expiration: ⤷  Sign Up

Formulations of 4-amino-2-(2,6-dioxopiperidine-3-yl)isoindoline-1,3-dione
Patent Number: ⤷  Sign Up
Patent Expiration: ⤷  Sign Up

FDA Regulatory Exclusivity protecting pomalyst

ADDITIONAL CLINICAL TRIAL INFORMATION ADDED TO PEDIATRIC USE SUBSECTION
Exclusivity Expiration: ⤷  Sign Up

FOR THE TREATMENT OF KAPOSI SARCOMA (KS) IN ADULT PATIENTS WHO ARE HIV-NEGATIVE
Exclusivity Expiration: ⤷  Sign Up

INDICATED FOR THE TREATMENT OF ADULT PATIENTS WITH AIDS-RELATED KAPOSI SARCOMA (KS) AFTER FAILURE OF HIGHLY ACTIVE ANTIRETROVIRAL THERAPY (HAART)
Exclusivity Expiration: ⤷  Sign Up

PEDIATRIC EXCLUSIVITY
Exclusivity Expiration: ⤷  Sign Up

PEDIATRIC EXCLUSIVITY
Exclusivity Expiration: ⤷  Sign Up

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Bristol POMALYST pomalidomide CAPSULE;ORAL 204026-004 Feb 8, 2013 AB RX Yes Yes ⤷  Sign Up ⤷  Sign Up Y ⤷  Sign Up
Bristol POMALYST pomalidomide CAPSULE;ORAL 204026-003 Feb 8, 2013 AB RX Yes No ⤷  Sign Up ⤷  Sign Up ⤷  Sign Up
Bristol POMALYST pomalidomide CAPSULE;ORAL 204026-004 Feb 8, 2013 AB RX Yes Yes ⤷  Sign Up ⤷  Sign Up Y ⤷  Sign Up
Bristol POMALYST pomalidomide CAPSULE;ORAL 204026-003 Feb 8, 2013 AB RX Yes No ⤷  Sign Up ⤷  Sign Up ⤷  Sign Up
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Exclusivity Expiration

Expired US Patents for pomalyst

Applicant Tradename Generic Name Dosage NDA Approval Date Patent No. Patent Expiration
Bristol POMALYST pomalidomide CAPSULE;ORAL 204026-001 Feb 8, 2013 ⤷  Sign Up ⤷  Sign Up
Bristol POMALYST pomalidomide CAPSULE;ORAL 204026-002 Feb 8, 2013 ⤷  Sign Up ⤷  Sign Up
Bristol POMALYST pomalidomide CAPSULE;ORAL 204026-004 Feb 8, 2013 ⤷  Sign Up ⤷  Sign Up
Bristol POMALYST pomalidomide CAPSULE;ORAL 204026-002 Feb 8, 2013 ⤷  Sign Up ⤷  Sign Up
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >Patent No. >Patent Expiration

EU/EMA Drug Approvals for pomalyst

Company Drugname Inn Product Number / Indication Status Generic Biosimilar Orphan Marketing Authorisation Marketing Refusal
Bristol-Myers Squibb Pharma EEIG Imnovid (previously Pomalidomide Celgene) pomalidomide EMEA/H/C/002682
Imnovid in combination with bortezomib and dexamethasone is indicated in the treatment of adult patients with multiple myeloma who have received at least one prior treatment regimen including lenalidomide.Imnovid in combination with dexamethasone is indicated in the treatment of adult patients with relapsed and refractory multiple myeloma who have received at least two prior treatment regimens, including both lenalidomide and bortezomib, and have demonstrated disease progression on the last therapy.
Authorised no no no 2013-08-05
>Company >Drugname >Inn >Product Number / Indication >Status >Generic >Biosimilar >Orphan >Marketing Authorisation >Marketing Refusal

International Patents for pomalyst

See the table below for patents covering pomalyst around the world.

Country Patent Number Title Estimated Expiration
Japan 2013209407 POLYMORPHIC FORMS OF 3-(4-AMINO-1-OXO-1,3 DIHYDRO-ISOINDOL-2-YL)-PIPERIDINE-2,6-DIONE ⤷  Sign Up
South Korea 20060087543 POLYMORPHIC FORMS OF 3-(4-AMINO-1-OXO-1,3 DIHYDRO-ISOINDOL-2-YL)-PIPERIDINE-2,6-DIONE ⤷  Sign Up
Argentina 102756 FORMAS POLIMÓRFICAS DE 3-(4-AMINO-1-OXO-1,3-DIHIDRO-ISOINDOL-2-IL)-PIPERIDIN-2,6-DIONA Y COMPOSICIONES QUE LAS COMPRENDEN ⤷  Sign Up
Russian Federation 2010137395 СПОСОБЫ ПРИМЕНЕНИЯ 3-(4-АМИНО-1-ОКСО-1,3-ДИГИДРОИЗОИНДОЛ-2-ИЛ)ПИПЕРИДИН-2,6-ДИОНА ДЛЯ ЛЕЧЕНИЯ ОПРЕДЕЛЕННЫХ ТИПОВ ЛЕЙКОЗА ⤷  Sign Up
>Country >Patent Number >Title >Estimated Expiration

Supplementary Protection Certificates for pomalyst

Patent Number Supplementary Protection Certificate SPC Country SPC Expiration SPC Description
2105135 212 50002-2015 Slovakia ⤷  Sign Up PRODUCT NAME: POMALIDOMID; REGISTRATION NO/DATE: EU/1/13/850/001 - EU/1/13/850/004 20130808
2105135 1590004-6 Sweden ⤷  Sign Up PRODUCT NAME: POMALIDOMIDE AND PHARMACEUTICALLY ACCEPTABLE SALTS, SOLVATES, HYDRATES OR STEREOISOMERS THEREOF; REG. NO/DATE: EU/1/13/850 20130808
2105135 5/2015 Austria ⤷  Sign Up PRODUCT NAME: POMALIDOMID UND SEINE PHARMAZEUTISCH AKZEPTABLEN SALZE, SOLVATE, HYDRATE ODER STEREOISOMERE; REGISTRATION NO/DATE: EU/1/13/850 20130805
0925294 07C0056 France ⤷  Sign Up PRODUCT NAME: LENALIDOMIDE; REGISTRATION NO/DATE: EU/1/07/391/001-004 20070618
>Patent Number >Supplementary Protection Certificate >SPC Country >SPC Expiration >SPC Description

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