[Skip navigation]FDA Logo links to FDA home page
Center for Drug Evaluation and Research, U.S. Food and Drug AdministrationU.S. Food and Drug AdministrationCenter for Drug Evaluation and Research
  HHS Logo links to Department of Health and Human Services website

FDA Home Page | CDER Home Page | CDER Site Info | Contact CDER | What's New @ CDER

horizonal rule
CDER Home About CDER Drug Information Regulatory Guidance CDER Calendar Specific Audiences CDER Archives
 
Powered by Google
 

 Oprelvekin

Product Approval Information - Licensing Action


Proper name: Oprelvekin
Tradename: Neumega
Manufacturer: Genetics Institute, Inc, Andover, MA, License #1163
Indication for Use: Prevention of severe thrombocytopenia and the reduction of the need for platelet transfusions following myelosuppressive chemotherapy in patients with nonmyeloid malignancies who are at high risk of severe thrombocytopenia
Approval Date: 11/25/97
Type of submission: Biologics license application


Approval Letter - (PDF), (Text)

Reviews - (PDF)
    Clinical (54 pages)
    Clinical pharmacokinetic (17 pages)
    CMC 1 (4 pages)
    CMC 2 (3 pages)
    Pharmacology (56 pages)
    Statistical (33 pages)

Talk Paper


Last Updated: 3/5/2001

 

Back to Top     Back to Index

Updated: September 25, 2003

horizonal rule