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Clinical trial

A Phase 2b, 8-Week, Double-Blind, Placebo-Controlled, Parallel-Group Study to Evaluate the Effects of 3 Different Dose Levels of IX-01 on Intravaginal Ejaculatory Latency Time (IELT), Patient-Reported Outcomes, and Safety in Men With Lifelong Premature Ejaculation (PE)

NCT03055806 is registered in ClinicalTrials.gov with Ixchelsis Limited as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
A Phase 2b, 8-Week, Double-Blind, Placebo-Controlled, Parallel-Group Study to Evaluate the Effects of 3 Different Dose Levels of IX-01 on Intravaginal Ejaculatory Latency Time (IELT), Patient-Reported Outcomes, and Safety in Men With Lifelong Premature Ejaculation (PE)
Lead sponsor
Ixchelsis Limited
Phase
Phase 2
Overall status
Completed
Start date
February 28, 2017
Completion date
December 6, 2017
Enrollment
239 (actual)
Sites
29

Conditions

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