CLINICAL_TRIALS
ClinicalTrials.gov record update
Phase 1, First-in-Human, Multicenter, Open-Label Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Preliminary Antitumor Activity of KO-2806 When Administered as Monotherapy and in Combination Therapy in Adult Patients With Advanced 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
- NCT06026410
- Title field or adapter rule
- {'original_value': 'Phase 1, First-in-Human, Multicenter, Open-Label Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Preliminary Antitumor Activity of KO-2806 When Administered as Monotherapy and in Combination Therapy in Adult Patients With Advanced Solid Tumors', 'source_field': 'protocolSection.identificationModule.officialTitle'}
- Ingested At
- 2026-10-31T23:27:23.483734+00:00
- Published At
- 2026-10-14T00:00:00+00:00
- Record Updated At
- 2026-10-14
- 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
["Solid Tumors With HRAS Alterations", "Non Small Cell Lung Cancer (NSCLC)", "Colorectal Cancer (CRC)", "Pancreatic Ductal Adenocarcinoma (PDAC)", "Clear Cell Renal Cell Carcinoma (ccRCC)", "Renal Cell Carcinoma (Kidney Cancer)", "Non Clear Cell Renal Cell Carcinoma (nccRCC)"]- protocolSection.statusModule.lastUpdatePostDateStruct
{"date": "2026-10-14", "type": "ACTUAL"}- protocolSection.identificationModule.nctId
"NCT06026410"- protocolSection.identificationModule.officialTitle
"Phase 1, First-in-Human, Multicenter, Open-Label Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Preliminary Antitumor Activity of KO-2806 When Administered as Monotherapy and in Combination Therapy in Adult Patients With Advanced Solid Tumors"- protocolSection.statusModule.overallStatus
"RECRUITING"- protocolSection.designModule.phases
["PHASE1"]- protocolSection.statusModule.resultsFirstPostDateStruct
null
Study condition terms
Interventions recorded in this study
- {'armGroupLabels': ['Arm #1: RAS-altered advanced solid tumors, monotherapy (escalation phase)', 'Arm #2: Advanced or metastatic RCC, combination therapy (escalation phase)', 'Arm #3: Advanced or metastatic NSCLC, CRC, or PDAC, combination therapy (escalation phase)', 'Arm #4: Advanced or metastatic ccRCC, combination therapy (expansion phase)', 'Arm #6: Advanced or metastatic ccRCC, cabozantinib rollover to combination therapy (expansion phase)', 'Arm #7: Advanced or metastatic NSCLC, combination therapy (expansion phase)'], 'description': 'Oral administration', 'name': 'Darlifarnib', 'type': 'DRUG'} (protocolSection.armsInterventionsModule.interventions[])
- {'armGroupLabels': ['Arm #2: Advanced or metastatic RCC, combination therapy (escalation phase)', 'Arm #4: Advanced or metastatic ccRCC, combination therapy (expansion phase)', 'Arm #5: Advanced or metastatic ccRCC, monotherapy (expansion phase)', 'Arm #6: Advanced or metastatic ccRCC, cabozantinib rollover to combination therapy (expansion phase)'], 'description': 'Oral administration', 'name': 'Cabozantinib', 'type': 'DRUG'} (protocolSection.armsInterventionsModule.interventions[])
- {'armGroupLabels': ['Arm #3: Advanced or metastatic NSCLC, CRC, or PDAC, combination therapy (escalation phase)', 'Arm #7: Advanced or metastatic NSCLC, combination therapy (expansion phase)'], 'description': 'Oral administration', 'name': 'Adagrasib', '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.