Arimidex in McCune Albright Syndrome

NCT00055302 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2015-09-01

No results posted yet for this study

Summary

The primary objective of this study is to evaluate the safety and efficacy of anastrozole 1 mg given once daily in subjects with McCune-Albright Syndrome.

Conditions

  • McCune-Albright Syndrome

Interventions

DRUG

Arimidex 1 mg

Arimidex (anastrozole) 1mg once daily by mouth

Sponsors & Collaborators

Principal Investigators

  • AstraZeneca Arimidex Medical Science Director, MD · AstraZeneca

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Max Age
10 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2002-08-31
Primary Completion
2006-02-28
Completion
2015-08-31

Countries

  • France
  • Germany
  • Italy
  • United Kingdom

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00055302 on ClinicalTrials.gov