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Completed

NCT Number: NCT03556956

Masitinib in Combination With FOLFIRI in Third or Fourth Line of Treatment of Patients With Metastatic Colorectal Cancer

A prospective, multicentre, open-label, randomized, phase 2-3 study to compare the efficacy and safety of masitinib in combination with FOLFIRI (irinotecan, 5-fluorouracil and folinic acid) versus Best Supportive Care, in third or fourth line treatment of patients with metastatic colorectal cancer

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2 / Phase 3

Primary location

University Hospital Olomouc, Olomouc, Czechia

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About this study

The objective is to compare the efficacy and safety of masitinib in combination with FOLFIRI (irinotecan, 5-fluorouracil and folinic acid) versus Best Supportive Care in third or fourth line treatment of patients with metastatic colorectal cancer.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patient with non-resectable metastatic colorectal cancer with histological or cytological documentation of adenocarcinoma of the colon or rectum.
  • Patient in third line or fourth line of treatment for metastatic colorectal cancer.
  • Patient with measurable lesions according to RECIST criteria (version 1.1).
  • Patient with ECOG equal to or less than 2.
  • Patient with adequate organ function
  • Other inclusion criteria may also apply

Exclusion criteria

  • Prior treatment with masitinib, or any other tyrosine kinase inhibitor for the treatment of malignancy, except regorafenib.
  • More than 3 prior chemotherapy regimens for metastatic colorectal cancer.
  • Pregnant, intent to be pregnant, or nursing female patient
  • Patient with any chronic inflammatory bowel disease
  • Patient treated for a cancer other than colorectal cancer within five years before enrollment, with the exception of basal cell carcinoma or cervical cancer in situ.
  • Other exclusion criteria may also apply

Treatment and study plan

Masitinib

Drug

Tyrosine kinase inhibitor

Other names: AB1010

Primary outcomes

  1. Overall survival

    Time frame: From day of randomization to death, assessed for a maximum of 60 months

    Overall survival (0S) is defined as time in months from the randomization date to the date of death due to any cause. If a patient is not known to have died, then OS will be censored at the date of last known date patient alive.

Secondary outcomes

  1. Survival rates

    Time frame: Every 24 weeks, assessed up to 60 months

    Survival rate, defined as the proportion of patients alive at each time point, estimated with Kaplan-Meier distribution

  2. Progression Free Survival (PFS)

    Time frame: From day of randomization to disease progression or death, whichever came first, assessed up to 60 months

    Progression Free Survival (PFS) is defined as the time from the randomization date until the date of earliest evidence of disease progression or death, for participants who progressed or died before subsequent cancer therapy. Disease progression will be assessed by the investigator on CT scan according to RECIST 1.1 criteria.

Sponsors and collaborators

Lead sponsor

AB Science

Industry

Registry information

Official study title

Masitinib in Combination With FOLFIRI Versus Masitinib Alone, Versus Best Supportive Care, in Third or Fourth Line of Treatment of Patients With Metastatic Colorectal Cancer

Important dates

Study start
2015
Primary completion
2020
Study completion
2020
First posted
Jun 14, 2018
Registry last updated
Dec 8, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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