CLINICAL_TRIALS
ClinicalTrials.gov record update
A Phase II Randomized Study of Adjuvant Versus NeoAdjuvant Pembrolizumab (MK-3475) for Clinically Detectable Stage III-IV High-Risk Melanoma
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
- NCT03698019
- Title field or adapter rule
- {'original_value': 'A Phase II Randomized Study of Adjuvant Versus NeoAdjuvant Pembrolizumab (MK-3475) for Clinically Detectable Stage III-IV High-Risk Melanoma', 'source_field': 'protocolSection.identificationModule.officialTitle'}
- Ingested At
- 2026-10-31T23:27:29.757860+00:00
- Published At
- 2023-11-21T00:00:00+00:00
- Record Updated At
- 2026-10-26
- Results Posted At
- 2023-11-21
- Source Retrieved At
- 2026-10-31T22:18:13.198083+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
["Acral Lentiginous Melanoma", "Clinical Stage III Cutaneous Melanoma AJCC v8", "Clinical Stage IV Cutaneous Melanoma AJCC v8", "Mucosal Melanoma"]- protocolSection.statusModule.lastUpdatePostDateStruct
{"date": "2026-10-26", "type": "ACTUAL"}- protocolSection.identificationModule.nctId
"NCT03698019"- protocolSection.identificationModule.officialTitle
"A Phase II Randomized Study of Adjuvant Versus NeoAdjuvant Pembrolizumab (MK-3475) for Clinically Detectable Stage III-IV High-Risk Melanoma"- protocolSection.statusModule.overallStatus
"ACTIVE_NOT_RECRUITING"- protocolSection.designModule.phases
["PHASE2"]- protocolSection.statusModule.resultsFirstPostDateStruct
{"date": "2023-11-21", "type": "ACTUAL"}
Study condition terms
Interventions recorded in this study
- {'armGroupLabels': ['Arm I (adjuvant pembrolizumab)', 'Arm II (adjuvant and neoadjuvant pembrolizumab)'], 'description': 'Undergo collection of blood', 'name': 'Biospecimen Collection', 'type': 'PROCEDURE'} (protocolSection.armsInterventionsModule.interventions[])
- {'armGroupLabels': ['Arm I (adjuvant pembrolizumab)', 'Arm II (adjuvant and neoadjuvant pembrolizumab)'], 'description': 'Undergo CT', 'name': 'Computed Tomography', 'type': 'PROCEDURE'} (protocolSection.armsInterventionsModule.interventions[])
- {'armGroupLabels': ['Arm I (adjuvant pembrolizumab)', 'Arm II (adjuvant and neoadjuvant pembrolizumab)'], 'description': 'Undergo MRI', 'name': 'Magnetic Resonance Imaging', 'type': 'PROCEDURE'} (protocolSection.armsInterventionsModule.interventions[])
- {'armGroupLabels': ['Arm I (adjuvant pembrolizumab)', 'Arm II (adjuvant and neoadjuvant pembrolizumab)'], 'description': 'Given IV', 'name': 'Pembrolizumab', 'type': 'BIOLOGICAL'} (protocolSection.armsInterventionsModule.interventions[])
- {'armGroupLabels': ['Arm I (adjuvant pembrolizumab)', 'Arm II (adjuvant and neoadjuvant pembrolizumab)'], 'description': 'Undergo surgery', 'name': 'Therapeutic Conventional Surgery', 'type': 'PROCEDURE'} (protocolSection.armsInterventionsModule.interventions[])
An intervention appearing in a study record does not establish an effect or an approved use.
This index keeps the source fields it imported; it may not contain the complete original record. Verify wording and context in the linked source.