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Clinical Trial of a MEK Inhibitor for RASopathy-Associated Severe Infantile Hypertrophic Cardiomyopathy: Baby MERIT

ConditionsHCMNoonan Syndrome and Other RasopathyHeart Failure (Pediatric)
Trial statusNot yet recruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age28-6
SponsorCarelon Research

About this trial

This project seeks to perform a Phase 3 clinical trial to test whether an FDA-approved cancer drug called trametinib is effective in treating young infants with genetic conditions called RASopathies and a severe, life-threatening heart problem called hypertrophic cardiomyopathy. The purpose of this research is to demonstrate that trametinib is effective in preventing these sick babies from dying, receiving a heart transplant or undergoing heart surgery to remove extra heart muscle over a one-year period. In addition, the investigators will determine how often this heart problem comes back when the trametinib treatment is stopped.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Molecular genetic diagnosis of a RASopathy signaling through the RAS/MAPK pathway as identified by molecular assays performed in a Clinical Laboratory Improvements of 1988 (CLIA) or similarly certified laboratories. Qualifying genotypes will included variants in any gene causing Noonan, Costello or cardiofaciocutaneous syndrome curated as pathogenic or likely pathogenic and consistent with the genetic mechanism (i.e., one allele in genes acting in an autosomal dominant manner and two alleles in trans for the autosomal recessive form of LZTR1-related Noonan syndrome).

Diagnosis of HCM, as defined by LV and interventricular septal wall thickness with a z-score > 2 by echocardiography

Age ≥ 28 days and ≤ 6 months

Ross classification of HF of III or IV

Disqualifiers

PTPN11 pathogenic/likely pathogenic variants causing NSML

Prior treatment with a MEK inhibitor

Requiring treatment with strong inhibitors of CYP2C19 and CYP3A4, strong inducers of CYP3A4, and substrates of CYP2C9 with a narrow therapeutic index

Platelet count < 50,000/µL

Trial design

Design model

Single group

Treatments tested in this trial

  • Trametinib

    Drug

    Participants will begin 0.025 mg/kg of oral trametinib once daily for up to 12 months. Dose will be adjusted for weight at each study visit. A 12-month surveillance phase follows cessation of treatment. If the participant experiences a RAS-HCM relapse during the surveillance phase, they will restart oral trametinib once daily for up to 12 additional months.

Treatment groups

25 Participants
are divided into 1 treatment group
Group A: TreatmentExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Time to first occurrence of death, heart transplantation, or LV septal myectomy to relieve LV outflow tract obstruction

This is a composite time-to-event outcome. An event is defined as the first occurrence of any of the following: death, heart transplantation, or LV septal myectomy to relieve LV outflow tract obstruction. For participants experiencing more than one component event, only the first event contributes to the primary endpoint. Participants who do not experience any component event are censored according to the prespecified analysis rules. The treatment arms will be compared using Kaplan-Meier methods and the log-rank test.

Time frame
From qualifying hospital admission through 12 months after the qualifying hospital admission

Secondary outcomes

1

Time from qualifying hospital admission to death

Time-to-event outcome defined as the time from the qualifying hospital admission to death from any cause. Participants who do not experience death during the assessment period will be censored according to the prespecified analysis rules. Treatment arms will be compared using Kaplan-Meier methods and the log-rank test.

Time frame
From qualifying hospital admission through 12 months after the qualifying hospital admission
2

Change from baseline in LV posterior wall thickness z-score at 12 months

Change in LV posterior wall z-score from baseline to 12 months. The change is calculated as the 12-month LV posterior wall z-score minus the baseline LV posterior wall z-score. Treatment groups will be compared using ANCOVA with treatment group as a fixed factor and baseline z-score as a covariate. All measurements and z-scores performed centrally at the Boston Children's Hospital Echocardiography Core Lab.

Time frame
Baseline and 12 months after qualifying hospital admission
3

Ross class at 12 months

Ross class is an ordinal measure with 4 categories (Class I-IV), with higher classes indicating greater severity of heart failure symptoms. Ross class at 12 months will be compared between the treatment arms using an ordinal regression model adjusted for baseline Ross class.

Time frame
12 months after qualifying hospital admission
4

Change from baseline in log-transformed BNP at 12 months

Change in log-transformed BNP from baseline to 12 months. The change is calculated as the 12-month value minus the baseline value. Treatment groups will be compared using ANCOVA with treatment group as a fixed factor and baseline log-transformed BNP/NT-proBN as a covariate.

Time frame
Baseline and 12 months after qualifying hospital admission

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Carelon Research

Lead sponsor

National Heart, Lung, and Blood Institute (NHLBI)

Collaborator

Source ClinicalTrials.gov

This trial is not recruiting at the moment. You can still explore other options: