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Hypertrophic Cardiomyopathy Symptom Release by BX1514M

Phase 2
Completed
Conditions
Hypertrophic Cardiomyopathy
Interventions
Drug: Placebo
Drug: Treatment BX1514M
Other: Walk distance test
Other: Exercise echocardiography
Registration Number
NCT02590809
Lead Sponsor
University Hospital, Bordeaux
Brief Summary

Hypertrophic cardiomyopathy (HCM) is the most frequent genetic cardiac disease characterized by an asymmetric hypertrophic. In two third of patients, an obstruction to blood ejection is observed within the left ventricle which is named left ventricular outflow tract obstruction (LVOTO). This phenomenon can occur at rest or during exercise and is associated with symptoms such as dyspnea, dizziness or chest pain that can significantly limit day life adaptation. To now, medical or interventional treatments such as betablocacker, calcium blockers or septal alcoholisation or surgery present with a limited efficiency. Recent studies from investigators group revealed new concepts about the role of venous return to the LVOTO. Therefore the investigators hypothesis that BX1514M generating a venous vascular constriction, could improve symptoms of HCM patients by reducing LVOTO.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
38
Inclusion Criteria
  • Patients with a typical or atypical hypertrophic cardiomyopathy (HCM) confirmed by imaging modalities (echo and MRI) and/or genetic tests or a relative history of HCM
  • Left ventricular obstruction during exercise on treadmill (above 50 mmHg)
  • Positive response to leg lifting test (obstruction reduction above 20 mmHg) at rest or in early recovery phase
  • Daily symptoms as shortness of breath during exercise (NYHA2-3), non coronary chest pain, dizziness
  • Correct ultrasound windows quality
  • Sinus rhythm
  • Optimal medical treatment
  • For women, pregnancy test or contraception
  • Written consent form obtained
Exclusion Criteria
  • Previous treatment by BX1514M
  • Extra-cardiac pathology with life expectancy below than 1 year
  • No capability of consent form written
  • Pregnancy women
  • Secondary hypertension hypertrophy, secondary valvular disease hypertrophy
  • Permanent atrial fibrillation
  • Severe ventricular arrhythmia without Implantable Cardioverter Defibrillator (ICD)
  • Severe coronary disease
  • Severe non stabilized hypertension
  • Severe cardiopathy (ejection fraction below 40% or demonstrated elevated end diastolic pressure or pulmonary pressure above 60 mmHg)
  • Bradycardia
  • Narrow angle glaucoma
  • Vascular prethrombotic diseases
  • Vascular spams
  • Thyrotoxicosis
  • Pheochromocytoma
  • Severe renal failure (<30ml/mn)
  • Patients at risk of urinary retention secondary to prostatic severe disease
  • Raynaud's disease
  • Non selective Monoamine Oxidase Inhibitors (MAOIs), iproniazid, nialamide or ephedrine, methylphenidate, phenylephrine, pseudoephedrine or digitalic
  • Procedures modifying the peripheral venous return
  • Participation to other research protocol

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Placebo groupPlacebo20 patients
Treatment groupWalk distance test20 patients
Treatment groupExercise echocardiography20 patients
Treatment groupTreatment BX1514M20 patients
Placebo groupWalk distance test20 patients
Placebo groupExercise echocardiography20 patients
Primary Outcome Measures
NameTimeMethod
Change from baseline at day 15 of covered distance during the 6 minutes walk distance test (6MWT)Day 15

In meters

Secondary Outcome Measures
NameTimeMethod
Covered distance during the 6 minutes walk distance test (6MWT)Day 30

In meters

Exercise echocardiography with measures of blood pressures in the rest and in the effortDay 1, day 15, day 30

Trial Locations

Locations (1)

CHU de Bordeaux

🇫🇷

Bordeaux, France

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