PGL4001 Efficacy Assessment in Reduction of Symptoms Due to Uterine Leiomyomata (Q63835591)

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clinical trial
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English
PGL4001 Efficacy Assessment in Reduction of Symptoms Due to Uterine Leiomyomata
clinical trial

    Statements

    PEARLIII (English)
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    A Phase III, Multicentre, Clinical Study Investigating the Efficacy and Safety of 3-months Open-label Treatment With PGL4001, Followed by a Randomised, Double-blind Placebo Controlled Period of 10 Days Treatment With Progestin, in Subjects With Myomas and Heavy Uterine Bleeding. (English)
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    July 2010
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    November 2011
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    209
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    18 year
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    48 year
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