Saturday, July 11, 2026

Drug profile · INN

sunvozertinib

sunvozertinib (ZEGFROVY) is an FDA-listed pharmaceutical active ingredient. Route of administration: oral. Current US regulatory status: approved.

FDA: approved NMPA: clinical trials
US status approved
Patents linked 0
Pipeline programs 5
News articles 0
Drug details — sunvozertinib
US status
approved
Class
Route
ORAL
Patents
0
Programs
5
Data quality
0.84

Quick answer

sunvozertinib (ZEGFROVY) is an FDA-listed pharmaceutical active ingredient. Route of administration: oral. Current US regulatory status: approved.

Key facts

INN sunvozertinib
Brand ZEGFROVY
Route ORAL
Formulation TABLET

Approval history

Authority Status Date
FDA approved
NMPA clinical trials

Pipeline programs

  1. Befotertinib combined Bevacizumab Phase 2 · Chinese Academy of · EGFR
  2. EGFR Antibody Phase 2 · First People's Hospital · Nasopharyngeal Cancinoma (NPC)
  3. Leuprorelin (GF) Phase 2 · Takeda · Uterine Fibroids
  4. Sunvozertinib Phase 2 · Chinese Academy of · Potentially Resectable EGFR Exon 20 Insertion Non-Small Cell
  5. Sunvozertinib, Sunvozertinib Phase 2 · Anaxis Pharma · Non-Small Cell Lung Cancer

Frequently asked questions

What is sunvozertinib?

sunvozertinib (ZEGFROVY) is an FDA-listed pharmaceutical active ingredient. Route of administration: oral. Current US regulatory status: approved.

What is the brand name for sunvozertinib?

ZEGFROVY is a marketed brand name for sunvozertinib. Check FDA Drugs@FDA for the current US label holder and prescribing information.

What is the US approval status of sunvozertinib?

sunvozertinib has approved status in the United States according to our Drugs@FDA-derived records. Verify on the official FDA label before clinical or commercial decisions.