Drug profile · INN
dacomitinib
VIZIMPRO
dacomitinib (VIZIMPRO) is a receptor protein-tyrosine kinase erbb-2 inhibitor. Route of administration: oral. Current US regulatory status: approved.
Drug details — dacomitinib
- US status
- approved
- Class
- Antineoplastic and immunomodulating agents (L01)
- Route
- ORAL
- Patents
- 0
- Programs
- 1
- Data quality
- 0.84
Quick answer
dacomitinib (VIZIMPRO) is a receptor protein-tyrosine kinase erbb-2 inhibitor. Route of administration: oral. Current US regulatory status: approved.
Key facts
Mechanism of action
Receptor protein-tyrosine kinase erbB-2 inhibitor
Primary target: Epidermal growth factor receptor
Approval history
| Authority | Status | Date |
|---|---|---|
| FDA | approved | — |
| EMA | approved | — |
| NMPA | clinical trials | — |
Pipeline programs
Related & competitor drugs
Frequently asked questions
What is dacomitinib?
dacomitinib (VIZIMPRO) is a receptor protein-tyrosine kinase erbb-2 inhibitor. Route of administration: oral. Current US regulatory status: approved.
What is the brand name for dacomitinib?
VIZIMPRO is a marketed brand name for dacomitinib. Check FDA Drugs@FDA for the current US label holder and prescribing information.
What is the US approval status of dacomitinib?
dacomitinib 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.