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Clinical trial

A Phase 1, Randomised, Open-label, 2-cohort, Cross-over Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of a Native Oral Testosterone Formulation (DITEST) in the Fed and Fasted State and Compared to Testosterone Undecanoate in Adult Men With Primary or Secondary Hypogonadism

NCT02966652 is registered in ClinicalTrials.gov with Neurocrine UK Limited as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
A Phase 1, Randomised, Open-label, 2-cohort, Cross-over Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of a Native Oral Testosterone Formulation (DITEST) in the Fed and Fasted State and Compared to Testosterone Undecanoate in Adult Men With Primary or Secondary Hypogonadism
Lead sponsor
Neurocrine UK Limited
Phase
Phase 1
Overall status
Completed
Start date
November 3, 2016
Completion date
October 4, 2018
Enrollment
25 (actual)
Sites
1

Conditions

As the registry lists them; a condition with its own page is linked.

male hypogonadism