- ICH GCP
- Registr klinických studií v USA
- Klinická studie NCT07927972
Study to Evaluate Pharmacokinetics, Safety, and Tolerability of Subcutaneous Injections of Elamipretide in Pediatric Subjects With Barth Syndrome (SPIBA-101)
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.
Přehled studie
Detailní popis
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.
Typ studie
Zápis (Odhadovaný)
Fáze
- Fáze 1
Kontakty a umístění
Studijní kontakt
- Jméno: Rekha Sathyanarayana
- Telefonní číslo: 617-762-2579
- E-mail: rekha.sathyanarayana@stealthbt.com
Kritéria účasti
Kritéria způsobilosti
Věk způsobilý ke studiu
- Dítě
- Dospělý
- Starší dospělý
Přijímá zdravé dobrovolníky
Pohlaví způsobilá ke studiu
Popis
Inclusion Criteria:
- 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.
- Agrees to adhere to the trial requirements for the length of the trial.
- Must have genetically confirmed Barth Syndrome (pathogenic variant in the TAZ gene)
- Male aged ≥ 1 year and weighing between 7 and 30 kg at time of the Baseline Visit
- 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.
- 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:
- 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.
- Current placement on the waiting list for heart transplantation.
- Hospitalization for heart failure within 6 months prior to the Screening/Baseline Visit
- 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.
- 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).
- 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.
- 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.
- History of allergic reaction to the IMP or any of its components.
Studijní plán
Jak je studie koncipována?
Detaily designu
- Primární účel: Léčba
- Přidělení: N/A
- Intervenční model: Přiřazení jedné skupiny
- Maskování: Žádné (otevřený štítek)
Zbraně a zásahy
Skupina účastníků / Arm |
Intervence / Léčba |
|---|---|
|
Experimentální: Elamipretide
SC injection daily |
SC injection daily
Ostatní jména:
|
Co je měření studie?
Primární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
|
Maximum plasma concentration of elamipretide and its metabolites
Časové okno: 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
Časové okno: 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
|
Sekundární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
|
Safety Assessments: Adverse Events and Serious Adverse Events
Časové okno: 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
Časové okno: 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
Časové okno: 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
Časové okno: 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
Časové okno: 4 weeks
|
Change in 12 Lead Electrocardiogram ECG heart Rate from Baseline |
4 weeks
|
|
Change in Vital Signs from Baseline: Temperature
Časové okno: 4 weeks
|
Change in temperature measure (Fahrenheit or Celsius) from baseline to week 4 |
4 weeks
|
|
Change in Vital Signs from Baseline: Respiratory Rate
Časové okno: 4 weeks
|
Change in respiratory rate (breaths per minute) from baseline to week 4 |
4 weeks
|
|
Change in Vital Signs from Baseline: Blood Pressure
Časové okno: 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
Časové okno: 4 weeks
|
Change in Heart Rate (beats per minute) from baseline to week 4 |
4 weeks
|
Spolupracovníci a vyšetřovatelé
Sponzor
Termíny studijních záznamů
Hlavní termíny studia
Začátek studia (Odhadovaný)
Primární dokončení (Odhadovaný)
Dokončení studie (Odhadovaný)
Termíny zápisu do studia
První předloženo
První předloženo, které splnilo kritéria kontroly kvality
První zveřejněno (Aktuální)
Aktualizace studijních záznamů
Poslední zveřejněná aktualizace (Aktuální)
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
Naposledy ověřeno
Více informací
Termíny související s touto studií
Klíčová slova
Další relevantní podmínky MeSH
- Kardiovaskulární choroby
- Srdeční choroba
- Metabolismus, vrozené chyby
- Genetické choroby, vrozené
- Metabolické choroby
- Vrozené vady
- Kardiovaskulární abnormality
- Srdeční vady, vrozené
- Abnormality, vícenásobné
- Poruchy metabolismu lipidů
- Genetická onemocnění, vázaná na X
- Metabolismus lipidů, vrozené chyby
- Vrozené, dědičné a neonatální nemoci a abnormality
- Nutriční a metabolické nemoci
- Barthův syndrom
- arginyl-2,'6'-dimethyltyrosyl-lysyl-fenylalaninamid
Další identifikační čísla studie
- SPIBA-101
Plán pro data jednotlivých účastníků (IPD)
Plánujete sdílet data jednotlivých účastníků (IPD)?
Informace o lécích a zařízeních, studijní dokumenty
Studuje lékový produkt regulovaný americkým FDA
Studuje produkt zařízení regulovaný americkým úřadem FDA
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