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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

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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

  • Solid Tumors With HRAS Alterations (protocolSection.conditionsModule.conditions)
  • Non Small Cell Lung Cancer (NSCLC) (protocolSection.conditionsModule.conditions)
  • Colorectal Cancer (CRC) (protocolSection.conditionsModule.conditions)
  • Pancreatic Ductal Adenocarcinoma (PDAC) (protocolSection.conditionsModule.conditions)
  • Clear Cell Renal Cell Carcinoma (ccRCC) (protocolSection.conditionsModule.conditions)
  • Renal Cell Carcinoma (Kidney Cancer) (protocolSection.conditionsModule.conditions)
  • Non Clear Cell Renal Cell Carcinoma (nccRCC) (protocolSection.conditionsModule.conditions)

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

  • Darlifarnib (protocolSection.armsInterventionsModule.interventions[].name)
  • Cabozantinib (protocolSection.armsInterventionsModule.interventions[].name)
  • Adagrasib (protocolSection.armsInterventionsModule.interventions[].name)

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

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