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Last Updated: November 21, 2019

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ELELYSO Drug Profile

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When do Elelyso patents expire, and when can generic versions of Elelyso launch?

Elelyso is a drug marketed by Pfizer and is included in one NDA. There are three patents protecting this drug.

This drug has seventy-eight patent family members in twenty-five countries.

The generic ingredient in ELELYSO is taliglucerase alfa. One supplier is listed for this compound. Additional details are available on the taliglucerase alfa profile page.

Summary for ELELYSO
International Patents:78
US Patents:3
Applicants:1
NDAs:1
Suppliers / Packagers: 1
Clinical Trials: 2
Drug Prices: Drug price information for ELELYSO
DailyMed Link:ELELYSO at DailyMed
Drug patent expirations by year for ELELYSO
Drug Prices for ELELYSO

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Generic Entry Opportunity Date for ELELYSO
Generic Entry Date for ELELYSO*:
Constraining patent/regulatory exclusivity:
NDA:
Dosage:
POWDER;IV (INFUSION)

*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.

Recent Clinical Trials for ELELYSO

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

SponsorPhase
Ari ZimranPhase 4
PfizerPhase 4

See all ELELYSO clinical trials

Pharmacology for ELELYSO

US Patents and Regulatory Information for ELELYSO

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Pfizer ELELYSO taliglucerase alfa POWDER;INTRAVENOUS 022458-001 May 1, 2012 RX Yes Yes   Start Trial   Start Trial Y Y   Start Trial
Pfizer ELELYSO taliglucerase alfa POWDER;INTRAVENOUS 022458-001 May 1, 2012 RX Yes Yes   Start Trial   Start Trial Y Y   Start Trial
Pfizer ELELYSO taliglucerase alfa POWDER;INTRAVENOUS 022458-001 May 1, 2012 RX Yes Yes   Start Trial   Start Trial   Start Trial
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Exclusivity Expiration

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