CLINICAL_TRIALS
ClinicalTrials.gov record update
A Phase 2, Open-Label, Master Protocol Study to Evaluate Safety and Efficacy of Treatment Combinations With Telisotuzumab Adizutecan in Subjects With Pancreatobiliary Cancers (AndroMETa-118)
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
- NCT07769502
- Title field or adapter rule
- {'original_value': 'A Phase 2, Open-Label, Master Protocol Study to Evaluate Safety and Efficacy of Treatment Combinations With Telisotuzumab Adizutecan in Subjects With Pancreatobiliary Cancers (AndroMETa-118)', 'source_field': 'protocolSection.identificationModule.officialTitle'}
- Ingested At
- 2026-10-31T23:27:23.523101+00:00
- Published At
- 2026-10-13T00:00:00+00:00
- Record Updated At
- 2026-10-13
- Source Retrieved At
- 2026-10-31T22:17:52.415050+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
["Pancreatobiliary Cancers", "Pancreatic Ductal Adenocarcinoma"]- protocolSection.statusModule.lastUpdatePostDateStruct
{"date": "2026-10-13", "type": "ACTUAL"}- protocolSection.identificationModule.nctId
"NCT07769502"- protocolSection.identificationModule.officialTitle
"A Phase 2, Open-Label, Master Protocol Study to Evaluate Safety and Efficacy of Treatment Combinations With Telisotuzumab Adizutecan in Subjects With Pancreatobiliary Cancers (AndroMETa-118)"- protocolSection.statusModule.overallStatus
"RECRUITING"- protocolSection.designModule.phases
["PHASE2"]- protocolSection.statusModule.resultsFirstPostDateStruct
null
Study condition terms
Interventions recorded in this study
- {'armGroupLabels': ['SS1: Dose Escalation: Telisotuzumab Adizutecan + Gemcitabine', 'SS1:DoseOptimization:TelisotuzumabAdizutecan+Gemcitabine DoseA', 'SS1:DoseOptimization:TelisotuzumabAdizutecan+GemcitabineDoseB'], 'description': 'Intravenous (IV) Infusion', 'name': 'Telisotuzumab Adizutecan', 'type': 'DRUG'} (protocolSection.armsInterventionsModule.interventions[])
- {'armGroupLabels': ['SS1: Dose Escalation: Telisotuzumab Adizutecan + Gemcitabine', 'SS1: Dose Optimization: Standard of Care (SOC)', 'SS1:DoseOptimization:TelisotuzumabAdizutecan+Gemcitabine DoseA', 'SS1:DoseOptimization:TelisotuzumabAdizutecan+GemcitabineDoseB'], 'description': 'Intravenous (IV) Infusion', 'name': 'Gemcitabine', 'type': 'DRUG'} (protocolSection.armsInterventionsModule.interventions[])
- {'armGroupLabels': ['SS1: Dose Optimization: Standard of Care (SOC)'], 'description': 'Intravenous (IV) Infusion', 'name': 'Nab-Paclitaxel', '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.