Lupron Depot (leuprolide acetate for depot suspension)
Company: Abbott Laboratories
Approval Status: Approved January 1996
Treatment for: prostate cancer
Areas: Endocrinology; Nephrology/Urology; Oncology
Possible similar drugs: Lupron Depot; Lupron Depot
| General Information | Clinical Results | Side Effects | Mechanism of Action |
General Information
A three month, 22.5 mg dosage of Lupron Depot was approved as a treatment for advanced-stage prostate cancer.
Clinical Results
In clinical trials, the safety and efficacy of Lupron Depot (three month, 22.5 mg) were similar to that of the original daily subcutaneous injection and the monthly depot formulation.
Side Effects
The most common side effect reported was hot flashes (58.5%). Like other treatment options, it may also cause impotence.
Mechanism of Action
Lupron Depot (three month, 22.5 mg) works by shutting down the production of the hormone testosterone, which plays a significant role in the growth of prostate cancer. Decreasing the levels of testosterone in the body also alleviates the bone pain and urinary problems that may be associated with metastatic prostate cancer.
The FDA drug information shown here is licensed from Thomson CenterWatch. The information provided here is for general educational purposes only and does not constitute medical or pharmaceutical advice which should be sought from qualified medical and pharmaceutical advisers.
