Phase I Study of PSD502 (Lidocaine Prilocaine Spray) Applied to the Glans Penis up to Three Times a Day for 21 Days in Healthy Male Volunteers

Phase 1

Completed

• Conditions: Healthy

• Registration Number: NCT00483990
• Lead Sponsor: Plethora Solutions Ltd

Brief Summary

The main objective of the study is to determine the safety and tolerability of repeated application of PSD502 to the glans penis in healthy male volunteers

Detailed Description

This is a phase I, double-blind, stratified, parallel group, placebo-controlled repeat dose study in a minimum of 8 circumcised and 8 uncircumcised healthy male volunteers. Subjects will attend 2 study visits, of which 1 will be a Screening Visit (Visit 1) and the other, a consecutive 21-day treatment visit (Visit 2; Days 1-21) which commences no more than 14 days after the Screening visit. Subjects will reside in the phase I unit throughout the treatment period. The duration of each subject's participation in the study will be up to 5 weeks.

Subjects are stratified based on whether they are circumcised or uncircumcised and within each stratified group subjects are randomized to PSD502 (lidocaine prilocaine spray) or placebo in a 3:1 ratio.

Procedures during the 21 day treatment period include: visual examination of the glans penis, blood sample collection for pharmacokinetic analysis of lidocaine and prilocaine, swabbing of the glans penis for residual PSD502, vital signs and 12-lead ECG, adverse event enquiries and collection of concomitant medications. Subjects are discharged from the clinic on Day 21 following a safety evaluation.

Study Timeline

• Study Start: 2007-03
• Primary Completion: 2007-06
• Study Completion: 2007-06
• Study First Submitted: 2007-06-06
• Study First Submitted QC: 2007-06-07
• Study First Posted: 2007-06-08
• Status Verified: 2010-07
• Last Update Submitted: 2010-07-14
• Last Update Posted: 2010-07-15

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Male
• Target Recruitment: 16

Inclusion Criteria

• Willing and able to provide written informed consent
• Male, aged 18 years and over
• In generally good health in the opinion of the Investigator
• Willing and able to comply with all study procedures in the opinion of the Investigator

Exclusion Criteria

• History of a significant medical condition that would preclude further study participation, in the opinion of the Investigator.
• Currently taking, or has taken within the 2 weeks prior to the Screening Visit, any concomitant medication that could confound interpretation of the safety data PSD502
• Suffering from an STD, or is positive for hepatitis B, hepatitis C, or HIV infection.
• Safety testing abnormalities at the Screening Visit, in particular liver function tests, that are indicative of a medical condition and that would preclude further participation, in the opinion of the Investigator.
• Significant abnormality of the glans penis that would preclude interpretation of the examination of the glans, or that could be worsened by use of PSD502.
• History of alcohol or drug abuse within 1 year prior to the Screening visit.
• Known drug sensitivity to amide-type local anesthetics.
• Use of an investigational (non-registered drug within 30 days of the Screening Visit.
• Unlikely to understand or be able to comply with study procedures, for any reason, in the opinion of the Investigator.
• History of Glucose-6-Phosphate Dehydrogenase (G-6-PD)deficiency or use of medications that would increase susceptibility to methemoglobinemia (e.g. anti-malarial agents).
• Use of class 1 (e.g. mexiletine, tocainide) and III (e.g. amiodarone, sotaolol)anti-arrhythmic drugs.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Safety based on: -Examination of glans penis -AEs & SAEs -Reasons for withdrawals -Use of concomitant medications -Vital signs & ECG -Urinalysis, hematology & biochemistry -Residual PSD502 on swabs

Trial Locations

Locations (1)

PRA International - Clinical Pharmacology Center; 🇺🇸 Lenexa, Kansas, United States