Last Updated: April 23, 2026

SUNVOZERTINIB - Generic Drug Details


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

Sunvozertinib is the generic ingredient in one branded drug marketed by Dizal Jiangsu and is included in one NDA. There are three patents protecting this compound. Additional information is available in the individual branded drug profile pages.

Sunvozertinib has thirty patent family members in sixteen countries.

Summary for SUNVOZERTINIB
International Patents:30
US Patents:3
Tradenames:1
Applicants:1
NDAs:1
Clinical Trials: 10
Patent Litigation and PTAB cases: See patent lawsuits and PTAB cases for SUNVOZERTINIB
DailyMed Link:SUNVOZERTINIB at DailyMed
DrugPatentWatch® Estimated Loss of Exclusivity (LOE) Date for SUNVOZERTINIB
Generic Entry Date for SUNVOZERTINIB*:
Constraining patent/regulatory exclusivity:
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.

Recent Clinical Trials for SUNVOZERTINIB

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

SponsorPhase
Dizal (Jiangsu) Pharmaceutical Co., Ltd.PHASE3
Dizal (Jiangsu) Pharmaceutical Co., Ltd.PHASE1
Dizal (Jiangsu) Pharmaceutical Co., Ltd.PHASE2

See all SUNVOZERTINIB clinical trials

US Patents and Regulatory Information for SUNVOZERTINIB

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Dizal Jiangsu ZEGFROVY sunvozertinib TABLET;ORAL 219839-001 Jul 2, 2025 RX Yes No ⤷  Start Trial ⤷  Start Trial Y Y ⤷  Start Trial
Dizal Jiangsu ZEGFROVY sunvozertinib TABLET;ORAL 219839-002 Jul 2, 2025 RX Yes Yes ⤷  Start Trial ⤷  Start Trial Y Y ⤷  Start Trial
Dizal Jiangsu ZEGFROVY sunvozertinib TABLET;ORAL 219839-002 Jul 2, 2025 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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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.