Safety, Tolerability and Pharmacokinetics (PK) Evaluation of BZ371A, Topically Administered

This is an interventional supportive care trial for Erectile Dysfunction Following Radical Prostatectomy focused on measuring Erectile Dysfunction, Radical Prostatectomy, Prostate Cancer Read More

Inclusion Criteria:

• Men or women
• Body mass index > 19 and < 28.5 Kg/m2
• Is able to understand the Informed Consent Form (ICF)

Exclusion Criteria:

• Women in their menstrual period;
• Diseases that interfere with the absorption, distribution and excretion of drugs, such as history or presence of hepatic or renal diseases;
• Presence of active genital lesions or sexually transmitted disease (STD) (such as herpes, gonorrhea, candidiasis, Human Papillomavirus, and others) that impair analysis of local adverse effects on the genitalia;
• History of symptomatic hypotension, or diseases that increase the risk of symptomatic hypotension, such as patients with heart disease (including a history of angina and/or heart failure) and nephropathies;
• Findings on ECG and/or laboratory tests that, in the investigator's judgment, are considered the research volunteer's participation or may interfere with the analysis of the study of the study;
• Blood pressure (BP) outside the limits considered safe: systolic BP (SBP) 90 - 140 mmHg and diastolic BP diastolic BP (DBP) 60 - 90 mmHg, except for situations such as "white coat syndrome";
• Any disease or condition or physical finding that the investigator considers significant and that increases the risk
• Any disease or condition or physical finding that the investigator considers significant and that increases the risk of participation of the research volunteer or may interfere with the results.