Wednesday, July 8, 2026

Drug profile · INN

eflapegrastim-xnst

eflapegrastim-xnst (ROLVEDON) is a granulocyte colony stimulating factor receptor agonist. Route of administration: subcutaneous. Current US regulatory status: approved.

FDA: approved
US status approved
Patents linked 0
Pipeline programs 0
News articles 0
Drug details — eflapegrastim-xnst
US status
approved
Class
Route
SUBCUTANEOUS
Patents
0
Programs
0
Data quality
0.84

Quick answer

eflapegrastim-xnst (ROLVEDON) is a granulocyte colony stimulating factor receptor agonist. Route of administration: subcutaneous. Current US regulatory status: approved.

Key facts

INN eflapegrastim-xnst
Brand ROLVEDON
Mechanism Granulocyte colony stimulating factor receptor agonist
Target Granulocyte colony-stimulating factor receptor
Route SUBCUTANEOUS
Formulation INJECTABLE

Mechanism of action

Granulocyte colony stimulating factor receptor agonist

Primary target: Granulocyte colony-stimulating factor receptor

Approval history

Authority Status Date
FDA approved

Related & competitor drugs

  1. filgrastim Antineoplastic and immunomodulating agents (L03)
  2. lipegfilgrastim Antineoplastic and immunomodulating agents (L03)
  3. pegfilgrastim-cbqv Granulocyte colony stimulating factor receptor agonist
  4. efbemalenograstim alfa-vuxw Granulocyte colony stimulating factor receptor agonist
  5. filgrastim-aafi Granulocyte colony stimulating factor receptor agonist
  6. filgrastim-ayow Granulocyte colony stimulating factor receptor agonist

Frequently asked questions

What is eflapegrastim-xnst?

eflapegrastim-xnst (ROLVEDON) is a granulocyte colony stimulating factor receptor agonist. Route of administration: subcutaneous. Current US regulatory status: approved.

What is the brand name for eflapegrastim-xnst?

ROLVEDON is a marketed brand name for eflapegrastim-xnst. Check FDA Drugs@FDA for the current US label holder and prescribing information.

What is the US approval status of eflapegrastim-xnst?

eflapegrastim-xnst 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.