Viewing Study NCT01252069


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Study NCT ID: NCT01252069
Status: COMPLETED
Last Update Posted: 2016-01-13
First Post: 2010-11-30
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: PGL4001 Efficacy Assessment in Reduction of Symptoms Due to Uterine Leiomyomata (PEARLIII-extension Study)
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Study Design

Study Type: INTERVENTIONAL
Expanded Access Type Individual: None
Expanded Access Type Intermediate: None
Expanded Access Type Treatment: None
Patient Registry: None
Target Duration: None
Design Allocation:
Design Intervention Model:
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Bio Spec Retention: None
Bio Spec Description: None
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Design Primary Purpose:
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Phases:

Phases

Phase Brief Phase Text View
None PHASE3 View
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