Efficacy of AB1010 in Patients With Systemic Indolent Mastocytosis

NCT00831974 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 23

Last updated 2018-12-11

No results posted yet for this study

Summary

This is a 12 weeks study aimed at assessing the safety and efficacy of 2 doses of AB1010 in patients suffering from indolent systemic mastocytosis with handicap.

Conditions

  • Mastocytosis

Interventions

DRUG

masitinib (AB1010)

3 mg/kg/day

DRUG

masitinib (AB1010)

6 mg/kg/day

Sponsors & Collaborators

  • AB Science

    lead INDUSTRY

Principal Investigators

  • Olivier Lortholary, MD, PhD · Hôpital Necker, Paris, France

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2004-10-31
Primary Completion
2007-02-28

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00831974 on ClinicalTrials.gov