CLINICAL_TRIALS
ClinicalTrials.gov record update
A Phase I, Open-Label, Multicenter Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Efficacy of YF550 in Participants With Locally Advanced or Metastatic Solid Tumors.
This page presents selected fields from the linked source record. It does not add a medical interpretation.
Record identity and dates
- Source
- ClinicalTrials.gov
- Source record ID
- NCT07894874
- Title field or adapter rule
- {'original_value': 'A Phase I, Open-Label, Multicenter Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Efficacy of YF550 in Participants With Locally Advanced or Metastatic Solid Tumors.', 'source_field': 'protocolSection.identificationModule.officialTitle'}
- Ingested At
- 2026-10-31T23:27:30.203481+00:00
- Published At
- 2026-10-26T00:00:00+00:00
- Record Updated At
- 2026-10-26
- Source Retrieved At
- 2026-10-31T22:18:22.973355+00:00
- Timestamp Basis
- ClinicalTrials.gov API/RSS response retrieval timestamp recorded by Dossier adapter
- Date limitation
- ClinicalTrials.gov API/RSS response retrieval timestamp recorded by Dossier adapter
Fields recorded by this source
- protocolSection.conditionsModule.conditions
["Solid Tumor (Phase I)", "Ovarian Cancer", "NSCLC (Advanced Non-small Cell Lung Cancer)", "TNBC - Triple-Negative Breast Cancer"]- protocolSection.statusModule.lastUpdatePostDateStruct
{"date": "2026-10-26", "type": "ACTUAL"}- protocolSection.identificationModule.nctId
"NCT07894874"- protocolSection.identificationModule.officialTitle
"A Phase I, Open-Label, Multicenter Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Efficacy of YF550 in Participants With Locally Advanced or Metastatic Solid Tumors."- protocolSection.statusModule.overallStatus
"NOT_YET_RECRUITING"- protocolSection.designModule.phases
["PHASE1"]- protocolSection.statusModule.resultsFirstPostDateStruct
null
Study condition terms
Interventions recorded in this study
- {'armGroupLabels': ['single arm study'], 'description': 'YF550 will be administered orally once daily in 21-day cycles,Treatment continues until disease progression, unacceptable toxicity, withdrawal of consent, or no further clinical benefit.', 'name': 'YF550', 'type': 'DRUG'} (protocolSection.armsInterventionsModule.interventions[])
An intervention appearing in a study record does not establish an effect or an approved use.
Drug names recorded in this source
A recorded drug name is not by itself an indication or a condition-specific relationship.
This index keeps the source fields it imported; it may not contain the complete original record. Verify wording and context in the linked source.