Last Updated: July 14, 2026

VEPPANU Drug Patent Profile


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

Veppanu is a drug marketed by Arvinas Operations and is included in one NDA. There are three patents protecting this drug.

This drug has fifty-four patent family members in twenty-three countries.

The generic ingredient in VEPPANU is vepdegestrant. Two suppliers are listed for this compound. Additional details are available on the vepdegestrant profile page.

DrugPatentWatch® Generic Entry Outlook for Veppanu

Veppanu will be eligible for patent challenges on May 1, 2030. This date may extended up to six months if a pediatric exclusivity extension is applied to the drug's patents.

By analyzing the patents and regulatory protections it appears that the earliest date for generic entry will be May 1, 2031. This may change due to patent challenges or generic licensing.

Indicators of Generic Entry

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Summary for VEPPANU
International Patents:54
US Patents:3
Applicants:1
NDAs:1
Finished Product Suppliers / Packagers: 2
Patent Applications: 348
What excipients (inactive ingredients) are in VEPPANU?VEPPANU excipients list
DailyMed Link:VEPPANU at DailyMed
DrugPatentWatch® Estimated Loss of Exclusivity (LOE) Date for VEPPANU
Generic Entry Date for VEPPANU*:
Constraining patent/regulatory exclusivity:

NEW CHEMICAL ENTITY

NDA:
Dosage:

TABLET;ORAL

*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 VEPPANU

VEPPANU is protected by three US patents and one FDA Regulatory Exclusivity.

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

This potential generic entry date is based on NEW CHEMICAL ENTITY.

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
Arvinas Operations VEPPANU vepdegestrant TABLET;ORAL 219835-001 May 1, 2026 RX Yes No 11,597,720 ⤷  Start Trial Y Y ⤷  Start Trial
Arvinas Operations VEPPANU vepdegestrant TABLET;ORAL 219835-002 May 1, 2026 RX Yes Yes 10,647,698 ⤷  Start Trial Y Y ⤷  Start Trial
Arvinas Operations VEPPANU vepdegestrant TABLET;ORAL 219835-001 May 1, 2026 RX Yes No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
Arvinas Operations VEPPANU vepdegestrant TABLET;ORAL 219835-002 May 1, 2026 RX Yes Yes ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
Arvinas Operations VEPPANU vepdegestrant TABLET;ORAL 219835-001 May 1, 2026 RX Yes No 10,899,742 ⤷  Start Trial ⤷  Start Trial
Arvinas Operations VEPPANU vepdegestrant TABLET;ORAL 219835-001 May 1, 2026 RX Yes No 10,647,698 ⤷  Start Trial Y 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

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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.