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Study to Evaluate Pharmacokinetics, Safety, and Tolerability of Subcutaneous Injections of Elamipretide in Pediatric Subjects With Barth Syndrome (SPIBA-101)

3. november 2026 oppdatert av: Stealth BioTherapeutics Inc.

A Phase 1 Open-Label Trial to Evaluate the Pharmacokinetics, Safety, and Tolerability of Subcutaneous Injections of Elamipretide in Pediatric Subjects With Genetically Confirmed Barth Syndrome

This Phase 1, open-label trial will enroll approximately 6 subjects who have BTHS weighing between 7 and 30 kg. Subjects will receive a weight-based dose of elamipretide daily via SC injection for 4 weeks. PK samples will be collected on Day 1 and at week 4 to determine PK profile in BTHS patients weighing between 7 and 30kg.

Studieoversikt

Status

Har ikke rekruttert ennå

Forhold

Intervensjon / Behandling

Detaljert beskrivelse

In this Phase 1, open-label trial to evaluate the PK, safety, and tolerability of elamipretide, approximately 6 pediatric subjects with genetically confirmed BTHS weighing between 7 and 30 kg will be enrolled to receive daily dosing via SC injection for 4 weeks.

To characterize the PK of elamipretide, PK sampling will be conducted at Day 1 and Week 4. The study is intended to characterize PK and safety across a broader range of body weights that haven't been studied in prior trials.

Studietype

Intervensjonell

Registrering (Antatt)

6

Fase

  • Fase 1

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Barn
  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Mann

Beskrivelse

Inclusion Criteria:

  1. Willing and able to provide signed informed consent form (ICF) prior to participation in any trial-related procedures. If applicable, informed consent in writing from parent(s) or legally-acceptable representative(s) and, informed assent from subject (if age appropriate according to local requirements) should be provided.
  2. Agrees to adhere to the trial requirements for the length of the trial.
  3. Must have genetically confirmed Barth Syndrome (pathogenic variant in the TAZ gene)
  4. Male aged ≥ 1 year and weighing between 7 and 30 kg at time of the Baseline Visit
  5. For subjects with a medical history of cardiomyopathy, must be on a stable regimen (unchanged and constant) of background heart failure medications for at least 3 months prior to the Screening Visit.
  6. Able to administer IMP or have an appropriate designee who can administer the IMP (i.e., a capable family member or a caregiver).

Exclusion Criteria:

  1. History of solid organ transplant, except successful cardiac transplantation >12 months prior to Screening, if, in the opinion of the Investigator, there is no evidence of organ rejection and post-transplant pharmacotherapy, the subject is stable, and participation in the trial does not pose additional safety risk.
  2. Current placement on the waiting list for heart transplantation.
  3. Hospitalization for heart failure within 6 months prior to the Screening/Baseline Visit
  4. Any disease or medical condition that in the opinion of the Investigator would prevent the subject from successfully participating in the trial and reliably completing the assessments or might confound trial results.
  5. eGFR of < 30 mL/min at the Screening Visit (for purposes of Screening, eGFR can be confirmed locally at the clinical site. Historical values within 3 months prior to Screening can be accepted).
  6. Active malignancy or any other cancer from which the subject has been cancer-free for < 2 years. Localized squamous or non-invasive basal cell skin carcinomas are allowed, if appropriately treated prior to Screening/Baseline.
  7. Participation in other investigational drug or device clinical trials within 30 days or 5 half-lives (whichever is longer) of Screening/Baseline; or is currently enrolled in a non-interventional clinical trial that, in the opinion of the Investigator, may be potentially confounding to the results of the current trial. NOTE: Subjects currently treated with elamipretide through an EAP are eligible to participate in the SPIBA-101 study.
  8. History of allergic reaction to the IMP or any of its components.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: N/A
  • Intervensjonsmodell: Enkeltgruppeoppdrag
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Elamipretide

SC injection daily

SC injection daily

Andre navn:
  • FORZINITY

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Maximum plasma concentration of elamipretide and its metabolites
Tidsramme: 24 hours

Characterization of the maximum plasma concentration (Cmax) of elamipretide and its metabolites utilizing population PK modeling.

24 hours
Area under the plasma concentration time curve from 0 to 24 hours
Tidsramme: 24 hours

Characterization of the area under the plasma concentration time curve from 0 to 24 hours of elamipretide and its metabolites (AUC0-24) utilizing population PK modeling.

24 hours

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Safety Assessments: Adverse Events and Serious Adverse Events
Tidsramme: 4 weeks

The incidence and severity of adverse events (AEs) and serious adverse events (SAEs) coded to system organ class and preferred term using the Medical Dictionary for Regulatory Activities (MedDRA) from baseline through 4 weeks. Report the # of subjects with adverse events and incidence and severity of such adverse events (AEs)

4 weeks
Change from baseline of Clinical Hematology
Tidsramme: 4 Weeks

Change from baseline in clinical hematology utilizing descriptive statistics of change relative to baseline and shift tables to show number of subjects who are low, normal, high at baseline verses week 4.

4 Weeks
Change in Clinical Chemistry from Baseline
Tidsramme: 4 weeks

Change from baseline in Clinical Chemistry utilizing descriptive statistics of change relative to baseline and shift tables to show number of subjects who are low, normal, high at baseline verses week 4.

4 weeks
Change in 12 Lead Electrocardiogram ECG QT Interval from Baseline
Tidsramme: 4 weeks

Change in findings of 12 Lead Electrocardiogram ECG QT Interval from baseline

4 weeks
Change in 12 Lead Electrocardiogram ECG heart rate from Baseline
Tidsramme: 4 weeks

Change in 12 Lead Electrocardiogram ECG heart Rate from Baseline

4 weeks
Change in Vital Signs from Baseline: Temperature
Tidsramme: 4 weeks

Change in temperature measure (Fahrenheit or Celsius) from baseline to week 4

4 weeks
Change in Vital Signs from Baseline: Respiratory Rate
Tidsramme: 4 weeks

Change in respiratory rate (breaths per minute) from baseline to week 4

4 weeks
Change in Vital Signs from Baseline: Blood Pressure
Tidsramme: 4 weeks

Change in resting (5 minutes) Blood Pressure (mm Hg) from baseline to week 4

4 weeks
Change in Vital Signs from Baseline: heart rate
Tidsramme: 4 weeks

Change in Heart Rate (beats per minute) from baseline to week 4

4 weeks

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

1. november 2026

Primær fullføring (Antatt)

1. mai 2027

Studiet fullført (Antatt)

1. juni 2027

Datoer for studieregistrering

Først innsendt

23. oktober 2026

Først innsendt som oppfylte QC-kriteriene

3. november 2026

Først lagt ut (Faktiske)

10. november 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

10. november 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

3. november 2026

Sist bekreftet

1. november 2026

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

UBESLUTTE

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Ja

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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