| Study summary: |
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Phase IIb/III, Randomized, Double-blind, Placebo Controlled
An Adaptive, phase 2b/3, Double-Blind, Randomized, Placebo controlled study to establish the dosage, efficacy, and safety of L-O-M® MCS in treating lower urinary tract symptoms suggestive of Benign Prostatic Hypeplasia.
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| Qualified participants must: |
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• Be male above 40 years of age
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Have a diagnosis of enlarged prostate with nocturia (urinating 2 or more times a night)
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| Participants may receive: |
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Medical care at no cost including:
- Study-related physical examination
- Laboratory blood analysis
- Investigational study drug to relieve enlarged prostate symptoms
Compensation for time & transportation
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