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OpenTrials
Completed

NCT Number: NCT01449162

Masitinib in Treatment of Patients With Severe Persistent Asthma Treated With Oral Corticosteroids

The study objective is to compare the efficacy and the safety of masitinib at 6 mg/kg/day versus placebo in the treatment of patients with Severe Persistent Asthma treated with oral corticosteroids.

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Key information

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Dr. Georgi Stranski University Hospital, Pleven, Bulgaria

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About this study

Masitinib is a selective tyrosine kinase inhibitor. It is known that activation of inflammatory cells, such as mast cells, and fibrous tissue remodeling are associated with c-Kit, Lyn and PDGFR kinase signaling pathways; all key targets of masitinib. The objective of this study is to compare the efficacy and safety of masitinib at 6 mg/kg/day versus matched placebo in severe persistent asthma patients that is uncontrolled with oral corticosteroids. The primary outcome measure will be severe asthma exacerbation rate over duration of the treatment.

Who can participate

Healthy volunteers accepted: No

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

Main inclusion criteria:

  • Patient with severe asthma and already treated with oral corticosteroids at a minimal daily dose of 7.5 mg prednisone or equivalent for at least 3 months prior to screening visit
  • Patient treated with oral corticosteroids during at least one period of 21 days, from 1 year prior to screening to 3 months before screening
  • Patient with no significant change in the regular asthma medication, no severe asthma exacerbation for at least 4 weeks prior to screening visit
  • Non-smoker patient for at least 1 year and with a prior tobacco consumption < 10 packs/year

Main exclusion criteria:

  • Patient with active lung disease other than asthma (e.g. chronic bronchitis)
  • Female patient who is pregnant or lactating
  • Asthmatic patient still exposed to allergens or to triggering factors influencing asthma control
  • Patient with history of acute infectious sinusitis or respiratory tract infection within 4 weeks prior to screening visit

Treatment and study plan

Masitinib

Drug

6 mg/kg/day

Other names: AB1010

Placebo

Drug

Other names: Placebo Oral Tablet

Primary outcomes

  1. Severe asthma exacerbation rate

    Time frame: Duration of patient treatment exposure, assessed until withdrawal from study, study completion date, or for a maximum of 60 months

    The number of severe asthma exacerbations over time frame of outcome measure

Secondary outcomes

  1. Asthma exacerbation rate

    Time frame: Duration of patient treatment exposure, assessed until withdrawal from study, study completion date, or for a maximum of 60 months

    The number of asthma exacerbations over time frame of outcome measure

  2. ACQ Score

    Time frame: 36 weeks

    Asthma Control Questionnaire (ACQ) Score

Sponsors and collaborators

Lead sponsor

AB Science

Industry

Registry information

Official study title

A Prospective, Multicenter, Randomised, Double-blind, Placebo-controlled, 2-parallel Groups, Phase 3 Study to Compare the Efficacy and the Safety of Masitinib at 6 mg/kg/Day Versus Placebo in the Treatment of Patients With Severe Persistent Asthma Treated With Oral Corticosteroids

Important dates

Study start
2011
Primary completion
2019
Study completion
2019
First posted
Oct 10, 2011
Registry last updated
Feb 10, 2021

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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