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Be Part of Research - Trial Details - A Study of Parenterally-administered Teverelix TFA in Healthy Male Volunteers

A Study of Parenterally-administered Teverelix TFA in Healthy Male Volunteers

Completed

Open to: MALE

Age: 40.0 - 70.0

Medical Conditions


This information is provided directly by researchers, and we recognise that it isn't always easy to understand. We are working with researchers to improve the accessibility of this information. In some summaries, you may come across links to external websites. These websites will have more information to help you better understand the study.


A Phase I, open-label, single centre study investigating the pharmacokinetics, safety and pharmacodynamics of a single dose of teverelix TFA, a gonadotrophin releasing hormone antagonist, via subcutaneous or intramuscular route of administration in healthy male volunteers

Start dates may differ between countries and research sites. The research team are responsible for keeping the information up-to-date.  

The recruitment start and end dates are as follows:

Nov 2018 Mar 2020

INTERVENTIONAL

Intervention Type : DRUG
Intervention Description : A single s.c. or i.m. injection of teverelix TFA administered on Day 1

Intervention Arm Group : 120 mg s.c.;60 mg s.c.;90 mg i.m.;90 mg s.c.;



You can take part if:



You may not be able to take part if:


This is in the inclusion criteria above


Below are the locations for where you can take part in the trial. Please note that not all sites may be open.

  • PAREXEL International Early Phase Clinical Unit (EPCU)
    London
    Middlesex
    HA1 3UJ


The study is sponsored by Antev Ltd.





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Read full details for Trial ID: NCT03781947
Last updated 16 March 2020

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