tamsulosin prolonged release
/ Generic mfg.
- LARVOL DELTA
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October 04, 2025
A Comparative Bioavailability Study of Tamsulosin 0.4 mg Prolonged-release Tablets Versus the Reference Drug Omnic Ocas®, Tamsulosin Hydrochloride 0.4 mg, Prolonged-release Film-coated Tablets, in Healthy Adult Male Subjects, Under Fasting Conditions
(clinicaltrials.gov)
- P1 | N=46 | Recruiting | Sponsor: Berlin-Chemie AG Menarini Group | Not yet recruiting ➔ Recruiting
Enrollment open
September 06, 2025
A Comparative Bioavailability Study of Tamsulosin 0.4 mg Prolonged-release Tablets Versus the Reference Drug Omnic Ocas®, Tamsulosin Hydrochloride 0.4 mg, Prolonged-release Film-coated Tablets, in Healthy Adult Male Subjects, Under Fasting Conditions
(clinicaltrials.gov)
- P1 | N=46 | Not yet recruiting | Sponsor: Berlin-Chemie AG Menarini Group
New P1 trial
August 28, 2025
A Comparative Bioavalability Study of Tamsulosin 0.4 mg Prolonged-release Tablets Versus the Reference Drug Omnic Ocas®, Tabsulosine 0.4 mg Tablets in Healthy Adult Male Subjects, at Steady State
(clinicaltrials.gov)
- P1 | N=33 | Active, not recruiting | Sponsor: Berlin-Chemie AG Menarini Group
New P1 trial
July 30, 2025
A Comparative Bioavailability Study of Tamsulosin 0.4 mg Prolonged-release Tablets Versus the Reference Drug Omnic Ocas®, Tamsulosin 0.4 mg Tablets, in Healthy Adult Male Subjects, Under Fed Conditions
(clinicaltrials.gov)
- P1 | N=46 | Recruiting | Sponsor: Berlin-Chemie AG Menarini Group
New P1 trial
August 09, 2025
A Comparative Bioavailability Study of Tamsulosin 0.4 mg Prolonged-release Tablets Versus the Reference Drug Omnic Ocas®, Tamsulosin 0.4 mg Tablets, in Healthy Adult Male Subjects, Under Fed Conditions
(clinicaltrials.gov)
- P1 | N=46 | Active, not recruiting | Sponsor: Berlin-Chemie AG Menarini Group | Recruiting ➔ Active, not recruiting
Enrollment closed
August 03, 2021
Antibiotic therapy effectiveness as an outcome predictor of complex treatment in chronic prostatitis/chronic pelvic pain syndrome.
(PubMed, Cent European J Urol)
- "All patients orally received: diclofenac sodium (100 mg/day, 2 weeks), modified release tamsulosin (0.4 mg/day, 1 month), and alcohol extract of Serenoa repens (320 mg/day, 6 months). For CP/CPPS, the history of antibiotic efficacy determines the prognosis of current treatment. The latent bacterial factor is assumed in 24.3-27% of cases of CP/CPPS."
Journal • CNS Disorders • Depression • Gynecology • Immunology • Inflammation • Mood Disorders • Musculoskeletal Pain • Pain • Psychiatry
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