View updated information about our visitor policy  »
Book an appointment at our COVID-19 Assessment Centre »

Cancer trials
Hospital  >  Care Programs  >  Odette Cancer Program  >  Clinical trials
Share:  
|

Trial details

A Randomized, Multicenter, Parallel-Group, Phase III Study to Compare the Efficacy of Arfolitixorin versus Leucovorin in Combination with 5-Fluorouracil, Oxaliplatin, and Bevacizumab in Patients with Advanced Colorectal Cancer

To find out more about this trial and your cancer treatment options, please speak with your doctor.

Trial short name: AGENT

Official title: A Randomized, Multicenter, Parallel-Group, Phase III Study to Compare the Efficacy of Arfolitixorin versus Leucovorin in Combination with 5-Fluorouracil, Oxaliplatin, and Bevacizumab in Patients with Advanced Colorectal Cancer

Principal Investigator: Dr. Michael Raphael

Cancer type: Gastrointestinal
Cancer location: Colorectal
Disease stage: Advanced Cancer
Trial phase: Phase 3
Intervention: Drug: Arfolitixorin, Drug: Leucovorin

Registration #: NCT03750786

Trial description:
The purpose of this study is to look at the effectiveness of the drug Arfolitixorin in combination with additional drugs (5-fluorouracil, oxaliplatin, and bevacizumab) in patients with colorectal cancer. Patients with advanced / metastatic colorectal cancer who meet certain criteria may be able to participate. There will be two groups of patients participating in this study; one group will receive Arfolitixorin in combination with additional drugs, while the other group will receive the drug Leucovorin in combination with additional drugs (standard of care). The doctor and study staff will not know which group a patient is in; patients will be randomized to receive one treatment or the other.

Inclusion Criteria: Colorectal adenocarcinoma verified by biopsy. Availability of biopsy material, from the primary tumor or metastasis, allowing for analysis of tumor gene expression. Non-resectable metastatic CRC planned for first line therapy with 5-FU, oxaliplatin, and bevacizumab. Evaluable disease with at least one measurable lesion of metastatic disease (≥10 mm in longest diameter on axial image on CT-scan or alternatively MRI with <5 mm reconstruction interval) obtained within 28 days of randomization. Life expectancy of more than 4 months. ECOG performance status 0 or 1. Hemoglobin (Hb) > 100 g/L, Absolute neutrophil count (ANC) > 1.5x109/L. Thrombocytes > 100x109/L. Creatinine clearance > 50 mL/min, Total bilirubin < 1.5 x ULN, AST and ALT < 3 x ULN (and < 5 x ULN in case of liver metastases). Male or female ≥18 years of age. Female patients of childbearing potential must have a negative urine pregnancy test and use adequate contraceptive measures . Male patients must use adequate contraceptive measures . Voluntarily signed informed consent before performance of any study related procedure not part of normal medical care, with the understanding that consent may be withdrawn by the patient at any time without prejudice to future medical care. Exclusion Criteria: Malignant tumors other than colorectal adenocarcinomas (current or within the previous five years), with the exception for curatively treated non-melanoma skin cancer or in situ carcinoma of the cervix. Less than 6 months between randomization and completion of the last anti-cancer treatment (chemotherapy/radiotherapy/immunotherapy/surgery, etc.). (NB: Rectal cancer treatment shorter than 8 weeks of chemo/radiation therapy is allowed.) Confirmation of progressive disease within 6 months after completion of prior anti cancer treatment. Indication for any metastatic Colo-rectal Cancer (mCRC) surgery or anti-cancer treatment other than study treatment. Prior treatment with arfolitixorin. Indication for treatment with a 5-FU analogue, or 5-FU for a condition other than mCRC. Known Dihydropyrimidine Dehydrogenase Deficiency (DPD) deficiency. Known or suspected central nervous system (CNS) metastases. Unresolved bowel obstruction, uncontrolled Crohn's disease, or ulcerative colitis. History of cardiac disease with a New York Heart Association Class II or greater, congestive heart failure, myocardial infarction, or unstable angina at any time during the 6 months prior to randomization, or serious arrhythmias requiring medication for treatment. Current CTCAE ≥ grade 3 diarrhea. Current chronic infection or uncontrolled serious illness causing immunodeficiency. Known or suspected hypersensitivity or intolerance to arfolitixorin, LV, 5-FU, oxaliplatin, or bevacizumab. Breastfeeding patients. Patient who received investigational drugs in other clinical trials within 28 days, or 5 half-lives of the investigational drug, prior to randomization. Patient with serious medical or psychiatric illness likely to interfere with participation in this clinical study. Ongoing drug or alcohol abuse, as deemed by the Investigator. Any condition that, in the opinion of the Investigator, could compromise the patient's safety or adherence to the study protocol. Involvement, or related to people involved in the planning or conduct of the study (applies to both Isofol Medical AB (publ) staff and staff at the study site)