Last Updated: July 8, 2026

EVDI Drug Patent Profile


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

Evdi is a drug marketed by Apotex and is included in one NDA. There is one patent protecting this drug.

This drug has one patent family member in one country.

The generic ingredient in EVDI is trabectedin. There are four drug master file entries for this compound. Two suppliers are listed for this compound. Additional details are available on the trabectedin profile page.

DrugPatentWatch® Generic Entry Outlook for Evdi

By analyzing the patents and regulatory protections it appears that the earliest date for generic entry will be February 18, 2043. This may change due to patent challenges or generic licensing.

There is one tentative approval for the generic drug (trabectedin), which indicates the potential for near-term generic launch.

Indicators of Generic Entry

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Summary for EVDI
International Patents:1
US Patents:1
Applicants:1
NDAs:1
Finished Product Suppliers / Packagers: 1
What excipients (inactive ingredients) are in EVDI?EVDI excipients list
DailyMed Link:EVDI at DailyMed
DrugPatentWatch® Estimated Loss of Exclusivity (LOE) Date for EVDI
Generic Entry Date for EVDI*:
Constraining patent/regulatory exclusivity:
NDA:
Dosage:

SOLUTION;INTRAVENOUS

*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.

Pharmacology for EVDI
Drug ClassAlkylating Drug
Mechanism of ActionAlkylating Activity

US Patents and Regulatory Information for EVDI

EVDI is protected by one US patents.

Based on analysis by DrugPatentWatch, the earliest date for a generic version of EVDI is ⤷  Start Trial.

This potential generic entry date is based on patent ⤷  Start Trial.

Generics may enter earlier, or later, based on new patent filings, patent extensions, patent invalidation, early generic licensing, generic entry preferences, and other factors.

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Apotex EVDI trabectedin SOLUTION;INTRAVENOUS 220837-001 May 1, 2026 RX Yes Yes ⤷  Start Trial ⤷  Start Trial Y ⤷  Start 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 EVDI

When does loss-of-exclusivity occur for EVDI?

Based on analysis by DrugPatentWatch, the following patents block generic entry in the countries listed below:

European Patent Office

Patent: 15184
Patent: COMPOSITION DE TRABECTÉDINE (TRABECTEDIN COMPOSITION)
Estimated Expiration: ⤷  Start Trial

Generics may enter earlier, or later, based on new patent filings, patent extensions, patent invalidation, early generic licensing, generic entry preferences, and other factors.

See the table below for additional patents covering EVDI around the world.

Country Patent Number Title Estimated Expiration
European Patent Office 4215184 COMPOSITION DE TRABECTÉDINE (TRABECTEDIN COMPOSITION) ⤷  Start Trial
>Country >Patent Number >Title >Estimated Expiration

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Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.