Method of treating benign prostatic hyperlasia with antibiotics
Disclosed are methods of improving the symptoms of mammals suffering from BPH using compositions containing one or more antibiotics. The method includes, but is not limited to, administering at least one antibiotic in one or more courses of treatment by one or more administration routes selected from intramuscularly, orally, intravenously, intrathecally, intratumorally, intranasally, topically, and transdermally, either alone or with a carrier to a mammal in need thereof.
1. A method of improving the symptoms of mammals suffering from BPH comprising administering to the mammal a composition comprising a therapeutically effective amount of one or more antibiotics, wherein the antibiotics are administered by administration of a course of a fluoroquinolone antibiotic, a course of metronidazole, and an intramuscular injection of an antibiotic selected from imipenem, gentamicin, and cephalothin.
2. The method of claim 1 , wherein the fluoroquinolone antibiotic is selected from the group consisting of ciprofloxacin, gemifloxacin, fosfomycin, levofloxacin, moxifloxacin, norfloxacin, ofloxacin, and derivatives and salts of any of the foregoing.
3. The method of claim 2 , wherein the fluoroquinolone antibiotic is selected from ciprofloxacin and levofloxacin.
4. The method of claim 1 , further comprising improving the International Prostate Symptom Score (IPSS) by lowering the mean IPSS from baseline by from 5 to 7 points, within one year.
5. The method of claim 1 , further comprising improving the mean IPSS score, when compared to the mean improvement in mean IPSS from oral medications for BPH, by an amount within the range of from about 30% to about 150% during the first year.
6. The method of claim 1 , further comprising improving the mean IPSS score, when compared to a placebo control, by an amount within the range of from about 75% to about 500% during the first year.
7. The method of claim 1 , further comprising improving the International Prostate Symptom Score (IPSS) by lowering the mean IPSS from baseline by from 4 to 5 points, within 42 months.
8. The method of claim 1 , further comprising improving the mean IPSS score, when compared to the mean improvement in mean IPSS from oral medications for BPH, by an amount within the range of from about 0 % to about 200% within 42 months.
9. The method of claim 1 , further comprising improving the mean IPSS score, when compared to a placebo control, by an amount within the range of from about 75% to about 350% within 42 months.
10. The method of claim 1 , further comprising improving the urinary peak flow rate (Qmax) by increasing the maximum urinary flow by an amount within the range of from about 1.3 to about 3.0 ml/sec within the first year.
11. The method of claim 1 , further comprising improving the mean Qmax, when compared to a placebo control, by an amount within the range of from about 100% to about 325% during the first year.
12. The method of claim 1 , further comprising administration of Fexapotide Triflutate and a pharmaceutically acceptable carrier.
13. The method of claim 12 , wherein Fexapotide Triflutate is administered by a route selected from the group consisting of intramuscularly, orally, intravenously, intrathecally, intratumorally, intranasally, topically, and transdermally.
14. The method of claim 1 , further comprising administration of a pharmaceutically active agent selected from the group consisting of tamsulosin, finasteride, terazosin, doxazosin, prazosin, tadalafil, alfuzosin, silodosin, dutasteride, combinations of dutasteride and tamsulosin, and mixtures and combinations thereof.
15. The method of claim 12 , further comprising administration of a pharmaceutically active agent selected from the group consisting of tamsulosin, finasteride, terazosin, doxazosin, prazosin, tadalafil, alfuzosin, silodosin, dutasteride, combinations of dutasteride and tamsulosin, and mixtures and combinations thereof.