Arimidex in McCune Albright Syndrome
NCT00055302 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 40
Last updated 2015-09-01
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
- lead INDUSTRY
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
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