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.
調査の概要
詳細な説明
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.
研究の種類
入学 (推定)
段階
- フェーズ 1
連絡先と場所
研究連絡先
- 名前:Rekha Sathyanarayana
- 電話番号:617-762-2579
- メール:rekha.sathyanarayana@stealthbt.com
参加基準
適格基準
就学可能な年齢
- 子
- 大人
- 高齢者
健康ボランティアの受け入れ
受講資格のある性別
説明
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.
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:なし
- 介入モデル:単一グループの割り当て
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的:Elamipretide
SC injection daily |
SC injection daily
他の名前:
|
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Maximum plasma concentration of elamipretide and its metabolites
時間枠: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
時間枠: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
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Safety Assessments: Adverse Events and Serious Adverse Events
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠:4 weeks
|
Change in 12 Lead Electrocardiogram ECG heart Rate from Baseline |
4 weeks
|
|
Change in Vital Signs from Baseline: Temperature
時間枠:4 weeks
|
Change in temperature measure (Fahrenheit or Celsius) from baseline to week 4 |
4 weeks
|
|
Change in Vital Signs from Baseline: Respiratory Rate
時間枠:4 weeks
|
Change in respiratory rate (breaths per minute) from baseline to week 4 |
4 weeks
|
|
Change in Vital Signs from Baseline: Blood Pressure
時間枠: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
時間枠:4 weeks
|
Change in Heart Rate (beats per minute) from baseline to week 4 |
4 weeks
|
協力者と研究者
研究記録日
主要日程の研究
研究開始 (推定)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
その他の研究ID番号
- SPIBA-101
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
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