Status:

COMPLETED

Effects of Triptorelin Pamoate in Children With Precocious Puberty - Follow up Study

Lead Sponsor:

Ipsen

Conditions:

Precocious Puberty

Eligibility:

All Genders

Phase:

PHASE3

Brief Summary

The purpose of the protocol is to assess the efficacy of triptorelin 11.25 mg with respect to the proportion of children who maintain a regression or stabilisation of sexual maturity until the end of ...

Eligibility Criteria

Inclusion

  • The child must have completed study 2-54-52014-143
  • The child must have an effective response to 2 injections of triptorelin 11.25 mg according to investigator's evaluation with no significant treatment side effects

Exclusion

  • The patient has a known hypersensitivity to any of the test materials or related compounds
  • The patient is unable or unwilling to comply fully with the protocol

Key Trial Info

Start Date :

April 1 2008

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

January 1 2016

Estimated Enrollment :

35 Patients enrolled

Trial Details

Trial ID

NCT00909844

Start Date

April 1 2008

End Date

January 1 2016

Last Update

January 15 2019

Active Locations (10)

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Page 1 of 3 (10 locations)

1

Hôpital Hôtel Dieu (CHU)

Angers, France, 49033

2

Medical Centre

Bordeaux, France, 33000

3

Hôpital Flaubert

Le Havre, France, 76083

4

Hôpital Archet II

Nice, France, 06202

Effects of Triptorelin Pamoate in Children With Precocious Puberty - Follow up Study | DecenTrialz