Wednesday, July 8, 2026

Drug profile · INN

amivantamab and hyaluronidase-lpuj

amivantamab and hyaluronidase-lpuj (RYBREVANT FASPRO) is an FDA-listed pharmaceutical active ingredient. Route of administration: single-use. Current US regulatory status: approved.

FDA: approved
US status approved
Patents linked 0
Pipeline programs 3
News articles 0
Drug details — amivantamab and hyaluronidase-lpuj
US status
approved
Class
Route
SINGLE-USE
Patents
0
Programs
3
Data quality
0.84

Quick answer

amivantamab and hyaluronidase-lpuj (RYBREVANT FASPRO) is an FDA-listed pharmaceutical active ingredient. Route of administration: single-use. Current US regulatory status: approved.

Key facts

INN amivantamab and hyaluronidase-lpuj
Brand RYBREVANT FASPRO
Route SINGLE-USE
Formulation INJECTION

Approval history

Authority Status Date
FDA approved

Pipeline programs

  1. DR200091 Phase 3 · Tour Hekla · Thrombotic episodes in superficial venous malformations in c
  2. IVA Phase 3 · Vertex Pharmaceuticals (Australia) · Cystic Fibrosis
  3. Quetiapine and placebo Approved · BRIGHT MINDS BIOSCIENCES · Bipolar Disorder

Frequently asked questions

What is amivantamab and hyaluronidase-lpuj?

amivantamab and hyaluronidase-lpuj (RYBREVANT FASPRO) is an FDA-listed pharmaceutical active ingredient. Route of administration: single-use. Current US regulatory status: approved.

What is the brand name for amivantamab and hyaluronidase-lpuj?

RYBREVANT FASPRO is a marketed brand name for amivantamab and hyaluronidase-lpuj. Check FDA Drugs@FDA for the current US label holder and prescribing information.

What is the US approval status of amivantamab and hyaluronidase-lpuj?

amivantamab and hyaluronidase-lpuj 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.