CLINICAL_TRIALS ClinicalTrials.gov record update

A Multi-Center, Placebo Controlled, Safety and Efficacy Study of the Selective Progesterone Receptor Modulator Proellex® (CDB-4124) in Anemic, Pre-Menopausal Women With Symptomatic Uterine Fibroids Requiring Hysterectomy

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Record identity and dates

Source: ClinicalTrials.gov
Source record ID: NCT00702702
Title field or adapter rule: protocolSection.identificationModule.officialTitle
Ingested At: 2026-04-28T10:35:38.574792+00:00
Published At: 2014-08-21T00:00:00+00:00
Record Updated At: 2014-08-21
Results Posted At: 2014-08-21
Timestamp Basis: source retrieval time was not retained by the feed adapter
Date limitation: source retrieval time was not retained by the feed adapter

protocolSection.conditionsModule.conditions: ["Uterine Fibroids", "Anemia"]
protocolSection.statusModule.lastUpdatePostDateStruct.date: "2014-08-21"
protocolSection.identificationModule.nctId: "NCT00702702"
protocolSection.identificationModule.officialTitle: "A Multi-Center, Placebo Controlled, Safety and Efficacy Study of the Selective Progesterone Receptor Modulator Proellex\u00ae (CDB-4124) in Anemic, Pre-Menopausal Women With Symptomatic Uterine Fibroids Requiring Hysterectomy"
protocolSection.statusModule.overallStatus: "TERMINATED"
protocolSection.designModule.phases: ["PHASE3"]
protocolSection.statusModule.resultsFirstPostDateStruct.date: "2014-08-21"

Intervention details are not present in the imported fields for this record. No drug-condition relationship is inferred from co-listing.

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