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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.

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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

  • Pancreatobiliary Cancers (protocolSection.conditionsModule.conditions)
  • Pancreatic Ductal Adenocarcinoma (protocolSection.conditionsModule.conditions)

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

  • Telisotuzumab Adizutecan (protocolSection.armsInterventionsModule.interventions[].name)
  • Gemcitabine (protocolSection.armsInterventionsModule.interventions[].name)
  • Nab-Paclitaxel (protocolSection.armsInterventionsModule.interventions[].name)

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.