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Efficacy and Safety of the DTT106 in the Treatment of Erectile Dysfunction Associated With Benign Prostatic Hyperplasia — AUSTRÁLIA  

Erectile Dysfunction Clinical Trial

Official title:
Phase III, Multicenter, Randomized, Double-blind Clinical Trial to Assess the Efficacy and Safety of the DTT106 in the Treatment of Erectile Dysfunction Associated With Benign Prostatic Hyperplasia

Clinical Trial Summary

The purpose of this study is to assess the safety and efficacy of the DTT106 in the treatment of erectile dysfunction associated with benign prostatic hyperplasia

Clinical Trial Description

After being informed about all risks and benefits and giving written informed consent, the subjects will undergo a 7-day screening to determine eligibility. After that, at visit 0 (V0), the subjects will be randomized to either the DTT106 or dutasteride + tamsulosin (0,5 mg + 0,4 mg). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06264414
Study type Interventional
Source EMS
Contact Cassiano Berto
Phone +551938877724
Email pesquisa.clinica@ncfarma.com.br
Status Not yet recruiting
Phase Phase 3
Start date February 2025
Completion date July 2027
View Details
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