Masitinib in Patients With Mastocytosis With Handicap and Bearing the D816V Mutation
Primary Purpose
Mastocytosis
Status
Completed
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
masitinib
Sponsored by
About this trial
This is an interventional treatment trial for Mastocytosis focused on measuring mastocytosis, D816V, handicaps
Eligibility Criteria
Inclusion Criteria:
Patients with one of the following documented mastocytosis:
- Smouldering systemic mastocytosis
- Indolent systemic mastocytosis with organomegaly
- Indolent Systemic Mastocytosis having 2 infiltrated organs (skin and bone-marrow)
- Any mastocytosis with in the last 6 months at least 3 anaphylactic shocks or syncops requiring either use of adrenaline or medical assistance
- Cutaneous Mastocytosis (CM)
Skin biopsy-documented mastocytosis and evaluable disease based upon:
- Histological criteria: typical infiltrates of mast cells in a multifocal or diffuse pattern in skin biopsy
- Clinical criteria: typical skin lesions (maculopapular, urticaria pigmentosa, mastocytoma)
- Missing data (c-kit molecular analysis not done) or documented presence of an activating point mutation in the phosphotransferase domain of c-kit such as D816V c-kit mutation in at least one infiltrated organ (bone marrow or skin)
Refractory to at least one of the symptomatic treatments such as:
- Anti H1
- Anti H2
- Proton pump inhibitor
- Osteoclast inhibitor
- Cromoglycate Sodium
- Antileukotriene
- Other therapies used for the symptomatic care
Handicap defined as at least one of the following handicaps:
- pruritus score ≥ 6
- number of flushes per week ≥ 7
- number of stools per day ≥ 4 ,
- number of mictions per day ≥ 8 ,
- QLQ-C30 score ≥ 60,
- Hamilton score ≥ 10
Exclusion Criteria:
Patients with one of the following mastocytosis:
- Systemic Mastocytosis with an Associated clonal Hematologic Non Mast cell lineage Disease (SM-AHNMD)
- Mast cell leukemia (MCL)
- Aggressive systemic mastocytosis (ASM)
- Patient with a major surgery within 2 weeks prior to study entry
No vulnerable population will be included in this study
- Life expectancy < 6 months.
- Patient is < 5 years free of malignancy, except treated basal cell skin cancer or cervical carcinoma in situ.
- Patient with grade III/IV cardiac problems as defined by the New York Heart Association Criteria. (i.e., congestive heart failure, myocardial infarction within 6 months of study)
- Patient has a severe and/or uncontrolled medical disease.
- Patient has a known diagnosis of human immunodeficiency virus (HIV) infection
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
masitinib 3 mg/kg/day
masitinib 6 mg/kg/day
Arm Description
masitinib 3 mg/kg/day
masitinib 6 mg/kg/day
Outcomes
Primary Outcome Measures
efficacy on handicaps
Pruritus score at week 12 Number of flushes per week at week 12 Hamilton score at week 12 Fatigue Impact scale at week 12
Secondary Outcome Measures
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01266369
Brief Title
Masitinib in Patients With Mastocytosis With Handicap and Bearing the D816V Mutation
Official Title
A 12-week With Possible Extension, Prospective, Multicenter, Randomized, Open-label, 2-parallel Group, Phase IIa Study to Compare Efficacy and Safety of AB1010 at 3 or 6 mg/kg/Day in Treatment of Patients With Mastocytosis With Handicap and Bearing Activating Point Mutations in the Phosphotransferase Domain of c-Kit Such as the Main Mutation Asp-816-Val (D816V)
Study Type
Interventional
2. Study Status
Record Verification Date
December 2018
Overall Recruitment Status
Completed
Study Start Date
February 2007 (undefined)
Primary Completion Date
November 2007 (Actual)
Study Completion Date
May 2010 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
AB Science
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The objective is to compare efficacy and safety of AB1010 at 3 or 6 mg/kg/day in treatment of patients with mastocytosis with handicap and bearing activating point mutations in the phosphotransferase domain of c-Kit such as the main mutation Asp-816-Val (D816V).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Mastocytosis
Keywords
mastocytosis, D816V, handicaps
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
21 (Actual)
8. Arms, Groups, and Interventions
Arm Title
masitinib 3 mg/kg/day
Arm Type
Experimental
Arm Description
masitinib 3 mg/kg/day
Arm Title
masitinib 6 mg/kg/day
Arm Type
Experimental
Arm Description
masitinib 6 mg/kg/day
Intervention Type
Drug
Intervention Name(s)
masitinib
Primary Outcome Measure Information:
Title
efficacy on handicaps
Description
Pruritus score at week 12 Number of flushes per week at week 12 Hamilton score at week 12 Fatigue Impact scale at week 12
Time Frame
week 12
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients with one of the following documented mastocytosis:
Smouldering systemic mastocytosis
Indolent systemic mastocytosis with organomegaly
Indolent Systemic Mastocytosis having 2 infiltrated organs (skin and bone-marrow)
Any mastocytosis with in the last 6 months at least 3 anaphylactic shocks or syncops requiring either use of adrenaline or medical assistance
Cutaneous Mastocytosis (CM)
Skin biopsy-documented mastocytosis and evaluable disease based upon:
Histological criteria: typical infiltrates of mast cells in a multifocal or diffuse pattern in skin biopsy
Clinical criteria: typical skin lesions (maculopapular, urticaria pigmentosa, mastocytoma)
Missing data (c-kit molecular analysis not done) or documented presence of an activating point mutation in the phosphotransferase domain of c-kit such as D816V c-kit mutation in at least one infiltrated organ (bone marrow or skin)
Refractory to at least one of the symptomatic treatments such as:
Anti H1
Anti H2
Proton pump inhibitor
Osteoclast inhibitor
Cromoglycate Sodium
Antileukotriene
Other therapies used for the symptomatic care
Handicap defined as at least one of the following handicaps:
pruritus score ≥ 6
number of flushes per week ≥ 7
number of stools per day ≥ 4 ,
number of mictions per day ≥ 8 ,
QLQ-C30 score ≥ 60,
Hamilton score ≥ 10
Exclusion Criteria:
Patients with one of the following mastocytosis:
Systemic Mastocytosis with an Associated clonal Hematologic Non Mast cell lineage Disease (SM-AHNMD)
Mast cell leukemia (MCL)
Aggressive systemic mastocytosis (ASM)
Patient with a major surgery within 2 weeks prior to study entry
No vulnerable population will be included in this study
Life expectancy < 6 months.
Patient is < 5 years free of malignancy, except treated basal cell skin cancer or cervical carcinoma in situ.
Patient with grade III/IV cardiac problems as defined by the New York Heart Association Criteria. (i.e., congestive heart failure, myocardial infarction within 6 months of study)
Patient has a severe and/or uncontrolled medical disease.
Patient has a known diagnosis of human immunodeficiency virus (HIV) infection
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Olivier Lortholary, MD, PhD
Organizational Affiliation
Necker Hospital, Paris, France
Official's Role
Principal Investigator
12. IPD Sharing Statement
Learn more about this trial
Masitinib in Patients With Mastocytosis With Handicap and Bearing the D816V Mutation
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