Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Peptide containing doai
Patent
1997-08-07
2000-04-25
Goldberg, Jerome D.
Drug, bio-affecting and body treating compositions
Designated organic active ingredient containing
Peptide containing doai
A61K 3800
Patent
active
060544325
ABSTRACT:
A regime for therapeutic management of a benign prostatic hyperplasia and prostatic cancer employs Cetrorelix alone or in combination with .alpha.-reductase inhibitors or .alpha.-receptor blocking agents. The regimen reduces the volume of the prostate and avoids the side effects associated with testosterone levels being in a castration range Cetrorelix is administered at dosages between 0,5 mg/day and 20 mg/week or about 0.014 mg/kg body weight per day to 0,30 mg/kg body weight per week or at levels of about 25 to 120 mg of Cetrorelix per month or 0.376 mg kg to 1.71 mg/kg per month Cetrorelix can be administered with .alpha.-reductase inhibitors or .alpha.-receptor blocking agents.
REFERENCES:
B. Lunenfeld, "The Basic Science of GnRH Analogues", Advances in the Study of GnRH Analogues, vol. 2, Nov. 1990, pp. 25-35.
Gormley, GJ, Stoner, E, WO9216233, "Combinations of 5-alpha-reductase inhibitor and antiandrogen--e.g. finasteride and flutamide, for synergistic treatment of protstatic cancer", MERI Mar. 20, 1991.
EP401653A, Boehringer Mannheim GMBH, "Medical Use of Naftopidil--for treating Dysuria Associated With Prostatic Hypertrophy", BOEF Jul. 06, 1989.
Gonzalez-Barcena et al.,"Responses to the Antagonistic Analog of LH-RH (SB-75, Cetrorelix) in Patients With Benign Prostatic Hyperplasia and Prostatic Cancer", The Prostate 24, 1994, pp. 84-92.
Oesterling, "Endocrine Therapies for Symptomatic Benign Prostatic Hyperplasia", Supplement to Urology, vol. 43, No. 2, Feb. 1994, pp. 7-16.
Engel Jurgen
Rawert Jurgen
Reissmann Thomas
Riethmuller-Winzen Hilde
Asta Medica Aktiengesellschaft
Goldberg Jerome D.
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