drugset / Trial / NCT04467697

Ambulatory Blood Pressure Monitoring (ABPM) Extension Study of Oral Testosterone Undecanoate in Hypogonadal Men

NCT04467697 ↗

Phase 3 Completed 155 enrolled Marius Pharmaceuticals Syneos Health · collab
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

EvaluationDrugModalityDoseRoute
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

Indications