Safety Study of Flavocoxid in Duchenne Muscular Dystrophy

NCT ID: NCT01335295

Last Updated: 2014-02-03

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 20 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2011-03-31
• Study Completion Date: 2013-12-31

Brief Summary

Objective of this study is to evaluate safety and tolerability of flavocoxid administered at the daily oral dose of 500 or 1000 mg/die for one year in DMD patients, alone or in association with steroids (deflazacort on alternate days) started at least one year before. The investigators will also perform a multidimensional clinical evaluation covering functional and muscle strength and quality of life (QoL)assessments.

Conditions

Duchenne Muscular Dystrophy

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Blinding Strategy: NONE

Interventions

Flavocoxid

Flavocoxid capsules TTD 500 mg/die or 1000 mg/die for 1 year

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• clinical diagnosis of DMD, confirmed by muscle biopsy and molecular analysis by MPLA;
• range of age between 4 -16 years;
• unaided ambulation for at least 75 meters, unassisted during the Screening 6MWT. Other personal assistance or use of assistive devices for ambulation (eg, short leg braces, long leg braces or walkers) is not permitted.
• follow-up of at least 1 year before baseline with the selected motor outcome measures;
• patients able to perform evaluation tests;
• patient legally authorized representative (LAR) able to understand and give the informed consent;
• absence of contra-indications to the use of flavocoxid (see below);
• written informed consent signed by LAR.

Exclusion Criteria

• treatment with other drugs analogue, similar or interacting with flavocoxid or immunosuppressive therapy (other than corticosteroids) within 3 months prior to start of study treatment;
• exposure to another investigational drug or supplements within 2 months prior to start of study treatment;
• presence of cognitive impairment that could influence the performance of the evaluation tests;
• history of major surgical procedure within 30 days prior to start of study treatment;
• expectation of major surgical procedure (eg, scoliosis surgery) during the 12-month treatment period of the study;
• ongoing participation in any other therapeutic clinical study;
• expectation of recruitment in the forthcoming exon-51 trial;
• requirement for daytime ventilator assistance;
• presence of liver-diseases or assumption of any hepatotoxic agent;
• screening laboratory values out of the laboratory ranges if clinically meaningful;
• prior or ongoing medical condition (eg, concomitant illness, psychiatric condition, behavioral disorder, alcoholism, drug abuse), medical history, physical findings, ECG findings, or laboratory abnormality that, in the investigator's opinion, could adversely affect the safety of the subject, makes it unlikely that the course of treatment or follow-up would be completed, or could impair the assessment of study results.

• Minimum Eligible Age: 4 Years
• Maximum Eligible Age: 16 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: No

Sponsors

University of Messina

OTHER

Sponsor Role: lead

Responsible Party

Giuseppe Vita

full professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Giuseppe Vita, MD

Role: PRINCIPAL_INVESTIGATOR

Department of Neuroscience, University of Messina

Locations

Department of Neuroscience, Psychiatry and Anestesiology, Policlinico of Messina

Messina, ME, Italy

Countries

Italy

Other Identifiers

DMD-2011

Identifier Type: -

Identifier Source: org_study_id