Rhucin Approval Status beta

  • FDA approved: No
  • Brand name: Rhucin
  • Generic name: recombinant human C1 esterase inhibitor
  • Company: Pharming Group NV
  • Treatment for: Angioedema

Rhucin (recombinant human C1 esterase inhibitor) is a human protein currently in development for the treatment of patients with acute attacks of Hereditary Angioedema (HAE).

FDA Approval Status for Rhucin

Feb 28, 2011Santarus and Pharming Announce Receipt of FDA Refusal to File Letter for Rhucin Biologics License Application
Dec 28, 2010Pharming And Santarus Announce Submission Of Rhucin Biologics License Application to FDA
Jan 29, 2008Pharming Provides Update on Rhucin

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

Severe allergies and anaphylaxis: Learn how epinephrine can save a life. Watch Video