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Hypertrophic Cardiomyopathy Symptom Release by BX1514M

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02590809
Acronym
Light-CARMIDO
Enrollment
38
Registered
2015-10-29
Start date
2015-10-07
Completion date
2016-07-06
Last updated
2026-05-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hypertrophic Cardiomyopathy

Keywords

Left ventricular obstruction

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.

Interventions

DRUGTreatment BX1514M

X mg x 3 /day of BX1514M for 15 days. Dosage will be then adapted, depending on symptoms release and walk distance test results for another 15 days period.

DRUGPlacebo

Placebo will be given for 30 days

OTHERWalk distance test

Walk distance test during 6 minutes

Sponsors

University Hospital, Bordeaux
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline at day 15 of covered distance during the 6 minutes walk distance test (6MWT)Day 15In meters

Secondary

MeasureTime frameDescription
Covered distance during the 6 minutes walk distance test (6MWT)Day 30In meters
Exercise echocardiography with measures of blood pressures in the rest and in the effortDay 1, day 15, day 30

Countries

France

Contacts

PRINCIPAL_INVESTIGATORStéphane LAFITTE, Pr

University Hospital, Bordeaux

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 15, 2026