An Efficacy and Safety Study of ABT-SLV176 for the Treatment of Hypogonadal Men
| Status: | Completed |
|---|---|
| Conditions: | Endocrine |
| Therapuetic Areas: | Endocrinology |
| Healthy: | No |
| Age Range: | 18 - 80 |
| Updated: | 5/5/2014 |
| Start Date: | March 2014 |
| End Date: | June 2015 |
| Contact: | Leasia Hill |
| Email: | leasia.hill@abbvie.com |
| Phone: | 847-938-0907 |
A Multicenter, Open-Label, Efficacy and Safety Study of ABT-SLV176 for the Treatment of Hypogonadal Men
This is an open-study with a 26 week open label treatment period followed by an optional 26
week open label extension. The total treatment period will be 52 weeks.
week open label extension. The total treatment period will be 52 weeks.
Inclusion Criteria:
Low testosterone
Exclusion Criteria:
- Normal testosterone levels
- Elevated Prostatic Specific Antigen (PSA)
- History of breast or prostate cancer
We found this trial at
41
sites
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