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Clinical Trial Summary

This study is a continuation of previous studies done in healthy volunteers to prove the efficacy of delivering Testosterone, the male hormone, rapidly across intact skin in s series of doses from low to high in men with low-to-no natural testosterone production to measure their response to the varying doses. The results of this study will inform further studies which will be longer in length, as to the starting doses. The study will be conducted in London, U.K. at the Advanced Therapies Centre, The London Clinic.


Clinical Trial Description

48 Patients will be enrolled following 2 independent verifying blood tests of their diagnosis of Hypogonadism. there will be 4 cohorts of 12 subjects, each receiving doses of the trail materials, titrated by means of number of sprays applied. Doses will range from 10 to 70 mgs Testosterone. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT01894308
Study type Interventional
Source Transdermal Delivery Solutions Corp
Contact Shern L. Chew, M.D., Ph.D.
Phone 011-44-20 034 6227
Email sl.chew@thelondonclinic.co.uk
Status Not yet recruiting
Phase Phase 2
Start date June 2024
Completion date February 2025

See also
  Status Clinical Trial Phase
Enrolling by invitation NCT02733133 - Product Transference Study of Testagen™ TDS®-Testosterone Phase 2