For Healthcare Professionals

KO-2806 Monotherapy and Combination Therapies in Advanced Solid Tumors

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About the study

This first-in-human (FIH) dose-escalation and dose-validation/expansion study will assess KO-2806, a farnesyl transferase inhibitor (FTI), as a monotherapy and in combination, in adult patients with advanced solid tumors.
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Who can take part

You may be eligible to participate in the study if you meet the following criteria:

INCLUSION CRITERIA

Inclusion Criteria:


  1. At least 18 years of age.
  2. Histologically or cytologically confirmed advanced solid tumors

  1. Arm #1 (Monotherapy): HRAS-mutant and/or amplified tumors (any solid tumor type); HRAS overexpression (only for HNSCC tumors); KRAS and/or NRAS, and/or HRAS-mutant and/or amplified NSCLC or CRC; KRAS-mutant and/or amplified PDAC
  2. Arm #2 (Combination): Must have received at least 1 prior systemic therapy with IO-based treatment for locally advanced or metastatic RCC
  3. Arm #3 (Combination): Must have KRAS G12C-mutant locally advanced or metastatic NSCLC, CRC, or PDAC and have received at least 1 prior systemic therapy for advanced or metastatic disease
  4. Measurable disease by Response Evaluation Criteria in Solid Tumors (RECIST) v1.1.
  5. Karnofsky Performance Status of 70 or higher with no clinically significant deterioration over the previous 2 weeks.
  6. Acceptable liver, renal, endocrine, and hematologic function.
  7. * Other protocol-defined inclusion criteria may apply.


EXCLUSION CRITERIA

Exclusion Criteria:


  1. Ongoing treatment with certain anticancer agents.
  2. Prior treatment with an FTI or HRAS inhibitor.
  3. Major surgery, other than local procedures, within 28 days prior to Cycle 1 Day 1, without complete recovery.
  4. Spinal cord compression, leptomeningeal disease, or clinically active CNS metastases.
  5. Toxicity (excluding alopecia) from prior therapy that has not been completely resolved to baseline at the time of consent.
  6. Active or prior documented autoimmune or inflammatory disorders within the past 5 years prior to Cycle 1 Day 1 (with exceptions).
  7. Active, uncontrolled bacterial, viral, or fungal infections requiring systemic therapy.
  8. Inability to swallow, impairment of gastrointestinal (GI) function or GI disease that may significantly alter the absorption of the trial drugs.
  9. Inadequate cardiac and/or vascular function, including receipt of treatment for unstable angina, myocardial infarction, and/or cerebro-vascular attack within the prior 6 months, mean QTcF ≥470 ms, or Class II or greater congestive heart failure.
  10. Other invasive malignancy within 2 years.
  11. * Other protocol-defined exclusion criteria may apply.


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Study Locations

Enter your ZIP code/Postal code/PIN code to locate study sites near you:

How to Apply


Contact the study center to learn if this study is a good match for you.
Phone iconCall 617-588-3755Email iconEmail Study Center

Study Details


Contition

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)

Age

18+

Phase

PHASE1

Participants Needed

270

Est. Completion Date

Apr 30, 2027

Treatment Type

INTERVENTIONAL


Sponsor

Kura Oncology, Inc.

ClinicalTrials.gov NCT Identifier

NCT06026410

Study Number

KO-2806-001

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