Clinical Trials Logo

Clinical Trial Summary

This study is to observe efficacy and safety after T-Gel 1% treatment in delayed puberty adolescents. Subjects who complete this trial may enter a 3 month extension study (UMD-01-090E).


Clinical Trial Description

n/a


Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms

  • Constitutional Delay in Growth and Puberty (CDGP)
  • Hypogonadism
  • Primary or Secondary Hypogonadism

NCT number NCT00193661
Study type Interventional
Source Solvay Pharmaceuticals
Contact
Status Completed
Phase Phase 2
Start date August 2002
Completion date March 2007

See also
  Status Clinical Trial Phase
Completed NCT00193700 - Pharmacokinetic Evaluation of Testosterone Gel (1%) Phase 1