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CLINICAL_TRIALS ClinicalTrials.gov record update

A Two Dose, Dose Escalation Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Effect on Vasomotor Symptoms of Q-122 in Female Subjects With Breast Cancer and Receiving an Aromatase Inhibitor or Tamoxifen

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT04080297
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-28T10:37:48.235293+00:00
Published At
2020-02-28T00:00:00+00:00
Record Updated At
2020-02-28
Results Posted At
2020-02-28
Timestamp Basis
source retrieval time was not retained by the feed adapter
Date limitation
source retrieval time was not retained by the feed adapter

Fields recorded by this source

protocolSection.conditionsModule.conditions
["Vasomotor Symptoms (VMS)"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2020-02-28"
protocolSection.identificationModule.nctId
"NCT04080297"
protocolSection.identificationModule.officialTitle
"A Two Dose, Dose Escalation Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Effect on Vasomotor Symptoms of Q-122 in Female Subjects With Breast Cancer and Receiving an Aromatase Inhibitor or Tamoxifen"
protocolSection.statusModule.overallStatus
"COMPLETED"
protocolSection.designModule.phases
["PHASE1"]
protocolSection.statusModule.resultsFirstPostDateStruct.date
"2020-02-28"

Study condition terms

  • Vasomotor Symptoms (VMS) (protocolSection.conditionsModule.conditions)

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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