drugset / Trial / NCT04467697
Ambulatory Blood Pressure Monitoring (ABPM) Extension Study of Oral Testosterone Undecanoate in Hypogonadal Men
NaSingle-groupOpen-labelTreatment
Summary
The purpose of this six-month treatment study is * to assess feasibility of a lower starting dose of SOV2012-F1 (daily dose of 400 mg \[200 mg with breakfast meal and 200mg with dinner meal\]) to titrate individual doses to further enhance efficacy and safety. * To examine the blood pressure (BP) effects of Marius's oral testosterone undecanoate formulation, SOV2012-F1, using 24-hour ambulatory blood pressure monitoring (ABPM).
Timeline
- Start
- 2018-09-18
- Primary completion
- 2020-05-01
- Completion
- 2020-05-01
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | SOV2012-F1 | Unknown | 100 mg | Oral |
| Subject | SOV2012-F1 | Unknown | 200 mg | Oral |
| Subject | SOV2012-F1 | Unknown | 400 mg | Oral |
| Subject | SOV2012-F1 | Unknown | 600 mg | Oral |
| Subject | SOV2012-F1 | Unknown | 800 mg | Oral |