CLINICAL_TRIALS ClinicalTrials.gov record update

A Feasibility Phase I Study of Therapeutic Drug Monitoring-Based Atezolizumab Dosing

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Record identity and dates

Source: ClinicalTrials.gov
Source record ID: NCT06066138
Title field or adapter rule: {'original_value': 'A Feasibility Phase I Study of Therapeutic Drug Monitoring-Based Atezolizumab Dosing', 'source_field': 'protocolSection.identificationModule.officialTitle'}
Ingested At: 2026-10-31T23:27:36.718162+00:00
Published At: 2026-10-16T00:00:00+00:00
Record Updated At: 2026-10-16
Source Retrieved At: 2026-10-31T22:19:02.163121+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

protocolSection.conditionsModule.conditions: ["Locally Advanced Alveolar Soft Part Sarcoma", "Metastatic Alveolar Soft Part Sarcoma", "Locally Advanced Non Small Cell Lung Cancer", "Metastatic Non Small Cell Lung Cancer", "Locally Advanced Small Cell Lung Cancer", "Metastatic Small Cell Lung Cancer", "Locally Advanced Hepatocellular Carcinoma", "Metastatic Hepatocellular Carcinoma", "Locally Advanced Melanoma", "Metastatic Melanoma"]
protocolSection.statusModule.lastUpdatePostDateStruct: {"date": "2026-10-16", "type": "ACTUAL"}
protocolSection.identificationModule.nctId: "NCT06066138"
protocolSection.identificationModule.officialTitle: "A Feasibility Phase I Study of Therapeutic Drug Monitoring-Based Atezolizumab Dosing"
protocolSection.statusModule.overallStatus: "RECRUITING"
protocolSection.designModule.phases: ["PHASE1"]
protocolSection.statusModule.resultsFirstPostDateStruct: null

{'armGroupLabels': ['Arm 1'], 'description': 'Atezolizumab administered via IV at either 1,200 mg q3 weeks, or 1,680 mg q4 weeks for the first 2 doses followed by 840mg q2 weeks or q6 weeks.', 'name': 'Atezolizumab', 'type': 'DRUG'} (protocolSection.armsInterventionsModule.interventions[])

An intervention appearing in a study record does not establish an effect or an approved use.

A recorded drug name is not by itself an indication or a condition-specific relationship.

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