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Clinical trial

A Phase I, Mono-center, Placebo and Comparator Controlled, Single-blind, Randomized, Parallel Group, Clinical Study to Determine Multiple Dose Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of FSH-GEX(TM) Administered Subcutaneously in Healthy Pituitary-suppressed Female Volunteers

NCT01477073 is registered in ClinicalTrials.gov with Glycotope GmbH as lead sponsor.

NCT NCT01477073
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Registry record

As filed in ClinicalTrials.gov.

Title
A Phase I, Mono-center, Placebo and Comparator Controlled, Single-blind, Randomized, Parallel Group, Clinical Study to Determine Multiple Dose Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of FSH-GEX(TM) Administered Subcutaneously in Healthy Pituitary-suppressed Female Volunteers
Lead sponsor
Glycotope GmbH
Phase
Phase 1
Overall status
Completed
Start date
October 31, 2011
Completion date
May 31, 2012
Enrollment
57 (actual)
Sites
1

Conditions

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

female infertility