- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving 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.
Studieoversikt
Status
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
Registrering (Antatt)
Fase
- Fase 1
Kontakter og plasseringer
Studiekontakt
- Navn: Rekha Sathyanarayana
- Telefonnummer: 617-762-2579
- E-post: rekha.sathyanarayana@stealthbt.com
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
- Barn
- Voksen
- Eldre voksen
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
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.
Studieplan
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:
|
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
Sponsor
Studierekorddatoer
Studer hoveddatoer
Studiestart (Antatt)
Primær fullføring (Antatt)
Studiet fullført (Antatt)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Faktiske)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
- Kardiovaskulære sykdommer
- Hjertesykdommer
- Metabolisme, medfødte feil
- Genetiske sykdommer, medfødte
- Metabolske sykdommer
- Medfødte abnormiteter
- Kardiovaskulære abnormiteter
- Hjertefeil, medfødt
- Abnormiteter, flere
- Lipidmetabolismeforstyrrelser
- Genetiske sykdommer, X-linked
- Lipidmetabolisme, medfødte feil
- Medfødte, arvelige og neonatale sykdommer og abnormiteter
- Ernæringsmessige og metabolske sykdommer
- Barth syndrom
- arginyl-2,'6'-dimetyltyrosyl-lysyl-fenylalaninamid
Andre studie-ID-numre
- SPIBA-101
Plan for individuelle deltakerdata (IPD)
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