Study of CMP-002 in Participants With SYNGAP1-Related Disorder (ASCEND)
A Double-blind, Randomized, Controlled, Multiple Ascending Dose Study of Intrathecally Administered CMP-002 in Participants With SYNGAP1-Related Disorder
The primary purpose of the study is to evaluate the safety, tolerability, and pharmacokinetics of CMP-002 in participants with SYNGAP1-related disorder.
調査の概要
詳細な説明
ASCEND is a global, Phase 1/2, multicenter, randomized, double-blind (Sponsor-open), controlled, multiple-ascending dose (MAD) study to assess the safety, tolerability, and pharmacokinetics, of CMP-002 in participants with SYNGAP1-related disorder (SRD). The study consists of a Baseline Period in which participants will undergo screening assessments to establish the baseline for clinical study assessments. The Baseline Period is followed by a Treatment Period consisting of 3 planned dose level cohorts wherein each participant will receive 3 doses of CMP-002 administered intrathecally (IT) or a control procedure on Days 1, 29, and 85. Each dose level cohort includes a minimum of 8 participants randomized in a 3:1 ratio (CMP-002: control). Following the completion of Dose 3, participants will be followed for an additional 24 weeks in the Follow-up Period.
研究の種類
入学 (推定)
段階
- フェーズ2
- フェーズ 1
連絡先と場所
研究連絡先
- 名前:CAMP4 Therapeutics Clinical Trials Information
- 電話番号:617-651-8867
- メール:medinfo@camp4tx.com
研究場所
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-
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Buenos Aires、アルゼンチン
- Hospital Alemán
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-
参加基準
適格基準
就学可能な年齢
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:
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Written informed consent and/or assent, according to local guidelines
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Participant is ≥2 and <18 years of age at the time of informed consent/assent
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Participants must have a clinical diagnosis of a SYNGAP1-related disorder. For entry into the treatment period, genetic confirmation (specifically, of protein truncating mutations in SYNGAP1 exons 5-19) is required. The following mutations in SYNGAP1 exons 5-19 are acceptable:
- Frameshift mutations
- Nonsense mutations
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Ability to comply with the protocol and trial procedures detailed in the Schedule of Assessments (SoA)
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Participant has phenotype consistent with haploinsufficiency
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Participants must be taking at least one maintenance ASM, have not made changes to ASMs dose or frequency for 6 weeks prior to entering the Baseline Period, and not be planning to change their anti-seizure regimen throughout the study
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For entry into Treatment Period: All maintenance ASMs and interventions for seizures, as well as any cannabinoid-based products, must have been stable (weight-related adjustments are allowed) during the Baseline Period
Exclusion Criteria:
- Participant has an exon 1-4, non-truncating mutation, missense mutations, and microdeletions that include the SYNGAP1 gene
- Participant's prior genetic test indicates a pathogenic or likely pathogenic variant in a gene other than SYNGAP1 (the pathogenic or likely pathogenic variant must be homozygous in cases of known recessive disease)
- Participant's genetic test indicates SYNGAP1 variant of unknown significance (VUS), mosaicism or additional genetic diagnoses
- Participant has a history of central nervous system (CNS) disease (other than epilepsy or SRD), including history of bacterial or viral meningitis or brain malformation
- History of intolerance of IT administration, including intolerance to lumbar puncture
- For entry into the Treatment Period: Participant has a spinal deformity or other condition that may alter the free flow of CSF or has an implanted CSF drainage shunt. Note: Participants with scoliosis or spinal rods are not excluded if, in the judgement of the Investigator, lumbar puncture can be performed and there is free flow of CSF.
- Participant has laboratory results outside of the normal ranges at screening and judged as clinically relevant by the Investigator for liver function (including GGT, alanine aminotransferase, aspartate aminotransferase, alkaline phosphatase), kidney function (creatinine, urea), and platelets
- Positive viral serology test results for HIV type 1 or 2 antibodies, hepatitis B surface antigen or hepatitis C virus (HCV) antibody
- Participant has participated in any other interventional clinical study of an investigational gene therapy, or participant is currently participating in or has participated in a clinical study involving an investigational medicinal product within 2 months (or 5 half-lives, whichever is longer) prior to Screening
- Participant is currently using or plans to use unapproved or experimental medicinal products or cannabinoid or cannabidiol or supplemental products, including acetyl-leucine related products
- Participant is using anticoagulants and antiplatelet agents; and is unwilling or unable to discontinue use per standard of care prior to and after the lumbar puncture dosing Day 1
- Participant has any other symptomatology of SRD disease or any disease or disorder, including a clinically significant unstable medical condition, CNS disease (other than epilepsy), or brain malformation, which in the opinion of the Investigator, may either put the participant at risk because of participation in the study including consideration of sedation procedures, may influence the results of the study, or may affect the participant's ability to participate in the study.
- Participant has known hypersensitivity to the excipients of the investigational medicinal product.
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:ランダム化
- 介入モデル:並列代入
- マスキング:4倍
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的:CMP-002 Multiple Ascending Dose (MAD)
Participants will be administered CMP-002 on Days 1, 29, and 85, and will be followed for 24 weeks after the last dose. Three dose levels will be evaluated. |
CMP-002 is an antisense oligonucleotide that will be administered by IT injection. |
|
偽コンパレータ:Sham-prick
Participants will receive the sham-prick procedure on Days 1, 29, and 85, and will be followed for 24 weeks after the last procedure. |
The sham-prick procedure involves no injection/puncture or penetration of the dura, but only a skin prick with a needle. |
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 |
時間枠 |
|---|---|
|
Safety and tolerability of multiple doses of CMP-002: incidence of adverse events and changes from baseline in clinical laboratory results
時間枠:Screening to Week 36
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Screening to Week 36
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二次結果の測定
結果測定 |
時間枠 |
|---|---|
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CSF concentrations of the active drug substance of CMP-002 after multiple doses
時間枠:Day 1 to Week 36
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Day 1 to Week 36
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Plasma PK of the active drug substance of CMP-002 after multiple doses: Cmax
時間枠:Day 1 to Day 85
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Day 1 to Day 85
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Plasma PK of the active drug substance of CMP-002 after multiple doses: AUC(0-24h)
時間枠:Day 1 to Day 85
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Day 1 to Day 85
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Urine PK of the active drug substance of CMP-002: Cmax
時間枠:Day 1
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Day 1
|
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Urine PK of the active drug substance of CMP-002: AUC(0-24hr)
時間枠:Day 1
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Day 1
|
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
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
米国FDA規制機器製品の研究
米国で製造され、米国から輸出された製品。
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