Magazine article Drug Topics

New Drug for Enlarged Prostate to Hit Pharmacies Next Month

Magazine article Drug Topics

New Drug for Enlarged Prostate to Hit Pharmacies Next Month

Article excerpt

Rx CARE

Men with benign prostatic hyperplasia (BPH) will soon have a therapeutic option that will reduce the risk of acute urinary retention and the need for BPH-related surgery while improving the symptoms of BPH.

Last month, the Food & Drug Administration approved the supplemental New Drug Application for dutasteride (Avodart, GlaxoSmithKline) for the treatment of BPH in men with an enlarged prostate. Dutasteride will be available in pharmacies in December.

As stated in the package insert (PI), the serum prostate specific antigen (PSA) will decrease by 20% within the first month of dutasteride therapy. The PSA value will be reduced by approximately 50% after six months of treatment, said Roehrborn.

The recommended dosage of dutasteride is one 0.5-mg softgel capsule taken daily by mouth, with or without food. Dosage adjustment is not necessary in older patients or in those with renal impairment.

The FDA based its approval on the results of three multicenter studies involving 4,325 men age 50 years or older, who had a serum PSA value of >= 1.5 ng/ml but < 10.0 ng/ml, as described in the PL Those enrolled in the study had a diagnosis of BPH, based on their medical history and a physical examination. Study data indicated that treatment with dutasteride reduced the risk of acute urinary retention and BPH-related surgery, improved BPH-related symptoms, decreased prostate volume, and increased maximum urinary flow rates.

Dutasteride originally received FDA approval in November 2001. According to Veronica Grosshandler, product communications manager for GlaxoSmithKline, the company delayed its launch of the product until approval of the sNDA in order to indude the two-year treatment data in the PI. The manufacturer wanted to provide the additional data to help healthcare providers make better decisions about the use of dutasteride in appropriate patients, she explained.

Claus Roehrborn, M.D., professor and chairman, department of urology, University of Texas Southwestern Medical Center, said that dutasteride is the first and only compound to inhibit both the type 1 and type 2 isoforms of the 5-alpha-reductase enzyme, which converts testosterone to dihydrotestosterone (DHT). DHT is known to be the primary cause of prostate growth.

The PI states that dutasteride should be used with caution in men taking potent inhibitors of the cytochrome P-450 3A4 (CYP3A4) isoenzyme, including ritonavir (Norvir, Abbott), ketoconazole, verapamil, diltiazem, cimetidine, and ciprofloxacin (Cipro, Bayer). …

Search by... Author
Show... All Results Primary Sources Peer-reviewed

Oops!

An unknown error has occurred. Please click the button below to reload the page. If the problem persists, please try again in a little while.