Study of Onvansertib in Combination With FOLFIRI and Bevacizumab Versus FOLFIRI and Bevacizumab for Second Line Treatment of Metastatic Colorectal Cancer in Participants With a Kirsten Rat Sarcoma Virus Gene (KRAS) or Neuroblastoma-RAS (NRAS) Mutation

NCT ID: NCT05593328

Last Updated: 2025-01-10

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 23 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-03-17
• Study Completion Date: 2024-12-09

Brief Summary

The primary objective of this study is to assess the efficacy of 2 different doses of onvansertib in combination with a chemotherapy regimen of irinotecan, fluorouracil [5-FU], and leucovorin (FOLFIRI) and bevacizumab for treatment of confirmed metastatic and/or unresectable colorectal cancer (CRC) in participants with a kirsten rat sarcoma virus gene (KRAS) or neuroblastoma-RAS (NRAS) mutation who have progressed on an oxaliplatin/fluoropyrimidinebased regimen in the first-line setting.

Conditions

Colorectal Cancer; Metastatic Colorectal Cancer

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Onvansertib 20 mg + Standard of Care (SOC)

Participants will receive 20 mg of onvansertib on Days 1 to 5 and 15 to 19 of a 28-day treatment cycle and SOC (FOLFIRI + bevacizumab) on Days 1 and 15 of each 28-day cycle.

Group Type: EXPERIMENTAL

Onvansertib

Intervention Type: DRUG

Oral capsule

FOLFIRI

Intervention Type: DRUG

FOLFIRI (irinotecan + fluorouracil \[5-FU\] + leucovorin) as intravenous (IV) infusion

Bevacizumab

Intervention Type: DRUG

IV infusion

Onvansertib 30 mg + Standard of Care (SOC)

Participants will receive 30 mg of onvansertib on Days 1 to 5 and 15 to 19 of a 28-day treatment cycle and SOC (FOLFIRI + bevacizumab) on Days 1 and 15 of each 28-day cycle.

Group Type: EXPERIMENTAL

Onvansertib

Intervention Type: DRUG

Oral capsule

FOLFIRI

Intervention Type: DRUG

FOLFIRI (irinotecan + fluorouracil \[5-FU\] + leucovorin) as intravenous (IV) infusion

Bevacizumab

Intervention Type: DRUG

IV infusion

Standard of Care (SOC)

Participants will receive SOC (FOLFIRI + bevacizumab) on Days 1 and 15 of each 28-day cycle.

Group Type: ACTIVE_COMPARATOR

FOLFIRI

Intervention Type: DRUG

FOLFIRI (irinotecan + fluorouracil \[5-FU\] + leucovorin) as intravenous (IV) infusion

Bevacizumab

Intervention Type: DRUG

IV infusion

Interventions

Onvansertib

Oral capsule

Intervention Type: DRUG

FOLFIRI

FOLFIRI (irinotecan + fluorouracil \[5-FU\] + leucovorin) as intravenous (IV) infusion

Intervention Type: DRUG

Bevacizumab

IV infusion

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Histologically confirmed metastatic and/or unresectable colorectal cancer (CRC).

2. Documentation of a kirsten rat sarcoma virus gene (KRAS) or neuroblastoma-RAS (NRAS) mutation in exon 2, 3, or 4 in primary tumor or metastasis, assessed by a Clinical Laboratory Improvement Amendments (CLIA)-certified laboratory.

3. Age ≥ 18 years.

4. Participants with tumors that have progressed on an oxaliplatin/fluoropyrimidine--based regimen with or without bevacizumab.

1. Participants must have had systemic therapy within 180 days of the screening visit.

2. Participants must have, at any time previously, received oxaliplatin-based chemotherapy with or without bevacizumab (≥ 6 weeks in duration).

3. Participants who received oxaliplatin/fluoropyrimidine-based neoadjuvant, adjuvant, and/or fluoropyrimidine maintenance or adjuvant therapy and have disease recurrence or progression > 6 months from their last dose of oxaliplatin will be required to have received oxaliplatin/fluoropyrimidine-based therapy with or without bevacizumab as first-line treatment for metastatic disease.

4. Participants who received an oxaliplatin-based regimen in the first-line setting and discontinued oxaliplatin because of toxicity or who received oxaliplatin for maintenance therapy are eligible as long as progression occurred < 6 months after the last dose of oxaliplatin therapy for advanced metastatic disease. It is recommended that these participants be re-challenged (if feasible) with oxaliplatin/fluoropyrimidine therapy and subsequently progress prior to eligibility. Participants with oxaliplatin-related neuropathy or oxaliplatin infusion-related hypersensitivity that cannot be rechallenged with oxaliplatin are eligible.

5. Participants must not have received prior treatment with irinotecan.

6. FOLFIRI therapy is appropriate for the participant as determined by the Investigator.

7. Imaging computed tomography (CT) or magnetic resonance imaging (MRI) of chest/abdomen/pelvis or other scans as necessary to document all sites of disease performed within 28 days prior to the first dose of onvansertib. Only participants with measurable disease as defined per Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST v1.1) are eligible for enrollment. CT is the preferred imaging modality, but MRI is also accepted. All subsequent scans must consistently use the same imaging modality for comparison with the Screening scan throughout the study.

8. Must have acceptable organ function

9. Signed informed consent to provide blood sample(s) for specific correlative assays

Exclusion Criteria

1. Concomitant KRAS or NRAS and BRAF-V600 mutation or Microsatellite Instability High/Deficient Mismatch Repair (MSI-H/dMMR).

2. Anti-cancer chemotherapy or biologic therapy administered within 28 days prior to the first dose of study drug. The exception is a single dose of radiation up to 8 Gray (equal to 800 RAD) with palliative intent for pain control up to 14 days before enrollment, provided it is not the target lesion.

3. More than 1 prior chemotherapy regimen administered in the metastatic setting.

4. Major surgery within 6 weeks prior to enrollment.

5. Untreated or symptomatic brain metastasis.

6. Gastrointestinal (GI) disorder(s) that, in the opinion of the Investigator, would significantly impede the absorption of an oral agent (e.g., intestinal occlusion, active Crohn's disease, ulcerative colitis, extensive gastric and small intestine resection).

7. Unable or unwilling to swallow study drug.

8. Known hypersensitivity to fluoropyrimidine or leucovorin.

9. Known hypersensitivity to irinotecan.

10. Abnormal glucuronidation of bilirubin; known Gilbert's syndrome.

11. QT interval:

1. Fridericia's correction (QTcF) > 470 milliseconds. The QTcF should be calculated as the arithmetic mean of the QTcF on triplicate electrocardiograms (ECGs). In the case of potentially correctible causes of QT prolongation that are readily corrected (e.g., medications, hypokalemia), the triplicate ECG may be repeated once during Screening and that result may be used to determine eligibility.

2. Planned concomitant use of medications known to prolong the QT/QTc interval according to institutional guidelines.

3. Presence of risk factors for torsade de pointes, including family history of Long QT Syndrome or uncorrected hypokalemia.

12. Use of strong cytochrome P450 3A4 (CYP3A4) or cytochrome P450 2C19 (CYP2C19) inhibitors or strong CYP3A4 inducers. Participants currently receiving these agents who can be switched to alternate therapy are not excluded. Inhibitors should be stopped at least 1 week prior to the first dose of protocol therapy and inducers should be stopped at least 2 weeks prior to initiation of protocol therapy.

1. History of cardiac disease: Congestive heart failure (CHF) Class II or higher according to the New York Heart Association (NYHA); active coronary artery disease, myocardial infarction within 6 months prior to study entry; unevaluated new onset angina within 3 months or unstable angina (angina symptoms at rest) or cardiac arrhythmias requiring anti-arrhythmic therapy, with the exception of participants who have been receiving therapy and are deemed by the Investigator to have stable/controlled disease.

2. Current uncontrolled hypertension (systolic blood pressure >150 mmHg or diastolic blood pressure >90 mmHg despite optimal medical management) and prior history of hypertensive crisis or hypertensive encephalopathy.

3. History of arterial thrombotic or embolic events (within 6 months prior to study entry).

4. Significant vascular disease (eg, aortic aneurysm, aortic dissection, symptomatic peripheral vascular disease).

5. Evidence of bleeding diathesis or clinically significant coagulopathy.

6. Major surgical procedure (including open biopsy, significant traumatic injury, etc) within 28 days, or anticipation of the need for major surgical procedure during the study, and minor surgical procedure (excluding placement of a vascular access device) within 7 days prior to study enrollment.

7. Proteinuria at Screening as demonstrated by urinalysis with proteinuria ≥2+ (participants discovered to have ≥2+ proteinuria on dipstick urinalysis at baseline should undergo a 24-hour urine collection and must demonstrate ≤1 g of protein in 24 hours to be eligible).

8. Abdominal fistula, gastrointestinal perforation, peptic ulcer, or intra-abdominal abscess within the past 6 months.

9. Ongoing serious, non-healing wound, ulcer, or bone fracture

10. Known hypersensitivity to any component of bevacizumab

11. History of reversible posterior leukoencephalopathy syndrome

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Cardiff Oncology

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Mayo Clinic in Arizona - Phoenix Campus

Phoenix, Arizona, United States

Central Arkansas Radiation Therapy Institute - Cancer Center

Little Rock, Arkansas, United States

Pacific Cancer Medical Center

Anaheim, California, United States

Comprehensive Blood and Cancer Center - Bakersfield

Bakersfield, California, United States

Cancer and Blood Specialty Clinic

Los Alamitos, California, United States

Norris Comprehensive Cancer Center

Los Angeles, California, United States

UCI Health - Chao Family Comprehensive Cancer Center

Orange, California, United States

UCLA Health - Santa Monica Parkside Cancer Care

Santa Monica, California, United States

Torrance Memorial Physician Network - Cancer Care and Infusion Center

Torrance, California, United States

PIH Health

Whittier, California, United States

Mayo Clinic - Jacksonville

Jacksonville, Florida, United States

Memorial Hospital West

Pembroke Pines, Florida, United States

Cancer & Hematology Centers of Western Michigan - Lemmen-Holton Cancer Pavilion

Grand Rapids, Michigan, United States

Mayo Clinic - Rochester

Rochester, Minnesota, United States

Washington University School of Medicine Center for Advanced Medicine

St Louis, Missouri, United States

Nebraska Cancer Specialists - Midwest Cancer Center - Legacy

Omaha, Nebraska, United States

Englewood Health

Englewood, New Jersey, United States

San Juan Oncology Associates

Farmington, New Mexico, United States

Manhattan Hematology Oncology Associates

New York, New York, United States

Gabrail Cancer and Research Center

Canton, Ohio, United States

Trihealth Kenwood

Cincinnati, Ohio, United States

University Hospitals Cleveland Medical Center

Cleveland, Ohio, United States

West Cancer Center - East Campus

Germantown, Tennessee, United States

University of Texas MD Anderson Cancer Center

Houston, Texas, United States

Utah Cancer Specialists

Salt Lake City, Utah, United States

University of Virginia School of Medicine

Charlottesville, Virginia, United States

Inova Schar Cancer Institute

Fairfax, Virginia, United States

Countries

United States

Other Identifiers

CRDF-003

Identifier Type: -

Identifier Source: org_study_id