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Clinical Trial Summary

Measure and evaluate the level of testosterone in blood, and determine the safety and tolerability following daily applications of testosterone gel. Subjects who complete this trial may participate in the extension part (UMD-01-080E).


Clinical Trial Description

n/a


Study Design

Allocation: Non-Randomized, Endpoint Classification: Pharmacokinetics 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 NCT00193700
Study type Interventional
Source Solvay Pharmaceuticals
Contact
Status Completed
Phase Phase 1
Start date August 2002

See also
  Status Clinical Trial Phase
Completed NCT00193661 - Observation Study of T-Gel (1%) in Treatment of Adolescent Boys With Hypogonadism Phase 2