Friday, July 10, 2026

Drug profile · INN

leuprolide mesylate

leuprolide mesylate (CAMCEVI KIT) is a gonadotropin-releasing hormone 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 — leuprolide mesylate
US status
approved
Class
Route
SUBCUTANEOUS
Patents
0
Programs
0
Data quality
0.84

Quick answer

leuprolide mesylate (CAMCEVI KIT) is a gonadotropin-releasing hormone receptor agonist. Route of administration: subcutaneous. Current US regulatory status: approved.

Key facts

INN leuprolide mesylate
Brand CAMCEVI KIT
Mechanism Gonadotropin-releasing hormone receptor agonist
Target Gonadotropin-releasing hormone receptor
Route SUBCUTANEOUS
Formulation EMULSION

Mechanism of action

Gonadotropin-releasing hormone receptor agonist

Primary target: Gonadotropin-releasing hormone receptor

Approval history

Authority Status Date
FDA approved

Related & competitor drugs

  1. cetrorelix acetate Gonadotropin-releasing hormone receptor antagonist
  2. elagolix Gonadotropin-releasing hormone receptor antagonist
  3. ganirelix acetate Gonadotropin-releasing hormone receptor antagonist
  4. leuprolide acetate Gonadotropin-releasing hormone receptor agonist
  5. abarelix Gonadotropin-releasing hormone receptor antagonist
  6. degarelix acetate Gonadotropin-releasing hormone receptor antagonist

Frequently asked questions

What is leuprolide mesylate?

leuprolide mesylate (CAMCEVI KIT) is a gonadotropin-releasing hormone receptor agonist. Route of administration: subcutaneous. Current US regulatory status: approved.

What is the brand name for leuprolide mesylate?

CAMCEVI KIT is a marketed brand name for leuprolide mesylate. Check FDA Drugs@FDA for the current US label holder and prescribing information.

What is the US approval status of leuprolide mesylate?

leuprolide mesylate 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.