- ICH GCP
- Registr klinických studií v USA
- Klinická studie NCT07740512
Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of PLX-200 in Pediatric Patients (Master Protocol)
28. července 2026 aktualizováno: Polaryx Therapeutics, Inc.
An Open-Label, Multicenter, Phase 2 Study to Evaluate Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of PLX-200 in Pediatric Patients With Lysosomal Storage Disorders (SOTERIA)
The purpose of this study is to evaluate the safety, tolerability and clinical activity of PLX-200 in pediatric patients with lysosomal storage disorders.
Přehled studie
Postavení
Zatím nenabíráme
Intervence / Léčba
Detailní popis
This is an open-label, proof-of-concept, Phase 2 basket trial evaluating the safety, tolerability, and clinical activity of PLX-200 in pediatric participants with lysosomal storage disorders (LSDs) including CLN2, CLN3, Sandhoff disease, and Krabbe disease.
Participants will receive PLX-200 oral solution twice daily (BID) for approximately 101 weeks, comprising of a 5-week Titration Period and 96-week Maintenance Period.
Clinical activity will be evaluated using synthetic control comparisons.
Dosing strategies and study durations for all other indications will be defined in their respective ISAs.
Typ studie
Intervenční
Zápis (Odhadovaný)
24
Fáze
- Fáze 2
Kontakty a umístění
Tato část poskytuje kontaktní údaje pro ty, kteří studii provádějí, a informace o tom, kde se tato studie provádí.
Studijní kontakt
- Jméno: Minsu Kang, PhD
- Telefonní číslo: 217-779-7736
- E-mail: minsukang@polaryx.com
Kritéria účasti
Výzkumníci hledají lidi, kteří odpovídají určitému popisu, kterému se říká kritéria způsobilosti. Některé příklady těchto kritérií jsou celkový zdravotní stav osoby nebo předchozí léčba.
Kritéria způsobilosti
Věk způsobilý ke studiu
- Dítě
Přijímá zdravé dobrovolníky
Ne
Popis
Inclusion Criteria:
- Male or female participants aged 2 to 15 years at the time of informed consent. Any deviations must be approved in advance by the Medical Monitor and Sponsor.
Genetically confirmed diagnosis of one of the four LSDs included in this study: CLN2, CLN3, Sandhoff disease or Krabbe disease. Diagnosis must be supported by all of the following:
- Age of symptom onset consistent with the targeted subtype,
- Relevant clinical manifestations, and
- Documented genotype at Screening or prior to enrollment. If no genotype is available at Screening, blood samples will be collected for genetic analysis as part of study procedures.
- Written informed consent must be obtained from the participant's parent(s) or legal guardian(s). Assent must also be obtained from the participant, when applicable, in accordance with local regulations and the participant's developmental status.
- Parent(s) or legal guardian(s) must demonstrate willingness and ability to comply with the protocol, including adherence to all required baseline, treatment, and follow-up assessments.
Exclusion Criteria:
- The participant has a known inherited neurologic disease other than the targeted lysosomal storage disorder subtype.
- The participant has a neurological illness unrelated to the study indication that may independently cause cognitive or motor decline.
- The participant requires ventilatory support, except for noninvasive support during sleep (e.g., Continuous Positive Airway Pressure [CPAP], Bilevel Positive Airway Pressure [BiPAP]).
- The participant has moderate or severe hepatic dysfunction, defined as alanine aminotransferase (ALT), aspartate aminotransferase (AST), or total bilirubin greater than 3 times the upper limit of normal (ULN), except in cases of Gilbert syndrome. The participant has a diagnosis of primary biliary cirrhosis.
- The participant has clinically significant anemia
- The participant has a body surface area (BSA)-adjusted eGFR <90 mL/min/1.73m2 at Screening or baseline.
- The participant has a history or current diagnosis of gallbladder disease (e.g., cholelithiasis or cholecystitis).
- The participant has a known hypersensitivity to gemfibrozil or any component of the study drug.
The participant is currently using, or is expected to require during the study, any of the following medications which are contraindicated with PLX-200:
- HMG-CoA reductase inhibitors
- Repaglinide (Prandin®)
- Dasabuvir (Exviera®)
- Selexipag (Uptravi®)
- Pioglitazone (Actos®)
- Fibrate medication (e.g., gemfibrozil, fenofibrate). Participants must not have received gemfibrozil or other fibrates for at least 2 weeks or five half-lives, whichever is shorter, before Visit 2 (Day 1). They may not receive gemfibrozil or other fibrates during the study
- Participants receiving Zavesca® (miglustat) or any other prohibited therapies must be willing to discontinue these therapies, complete a washout period (2 weeks or five half-lives, whichever is shorter) prior to Visit 2 (Day 1), and refrain from receiving them while they are participating in the study. If participants were previously on Brineura®, they must complete a 3-month washout period prior to Visit 2 (Day 1) and refrain from receiving it while they are participating in the study.
- The participant has a medical condition or personal circumstance that, in the opinion of the Investigator or Sponsor, could compromise safety, protocol compliance, or the interpretability of study data.
- The participant has received any investigational product or medical device within 30 days prior to the baseline visit that could confound study results or pose additional risk. All participants who have previously received stem cell or gene therapy are excluded regardless of timing.
- The participant receives systemic anticoagulant therapy (e.g., warfarin) and is unable or unwilling to comply with increased frequency of INR monitoring during study participation. Note: Participants may be eligible if receiving anticoagulants (e.g., warfarin) provided that INR can be monitored with increased frequency and dose adjustments are implemented to maintain therapeutic range and avoid bleeding complications.
- The participant has uncontrolled seizures, defined as ≥4 generalized tonic-clonic seizures per month or a recent episode of status epilepticus.
- The participant has severe central nervous system abnormalities (e.g., hydrocephalus, intracranial shunt).
- The participant has a history of clinically significant arrhythmia or QTc prolongation at Screening or baseline.
- The participant is pregnant or breastfeeding or is a female showing signs of pubertal development (e.g., Tanner Stage ≥2) who is unable or unwilling to undergo pregnancy testing at Screening or baseline. All such determinations must involve consultation with the Medical Monitor and follow the procedures outlined in each ISA.
Studijní plán
Tato část poskytuje podrobnosti o studijním plánu, včetně toho, jak je studie navržena a co studie měří.
Jak je studie koncipována?
Detaily designu
- Primární účel: Léčba
- Přidělení: Nerandomizované
- Intervenční model: Přiřazení jedné skupiny
- Maskování: Žádné (otevřený štítek)
Zbraně a zásahy
Skupina účastníků / Arm |
Intervence / Léčba |
|---|---|
|
Experimentální: PLX-200 (CLN3 Disease Cohort)
An Open-Label, Multicenter, Phase 2 Study to Evaluate Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of PLX-200 in Pediatric Patients with CLN3 Disease (Juvenile Neuronal Ceroid Lipofuscinosis) (CLN3 Intervention-Specific Assessment [ISA] Under the PLX-200-600 Master Protocol)
|
PLX-200 will be BID, with equal doses given approximately 12 hours apart, 30 minutes before the morning and evening meals, for 101 weeks (5-week Titration Period and 96-week Maintenance Period) based on each participant's weight.
Dosing will begin with a 5-week TP based on the participant's weight group to achieve a target maintenance dose (TMD).
Ostatní jména:
|
|
Experimentální: PLX-200 (CLN2 Disease Cohort)
An Open-Label, Multicenter, Phase 2 Study to Evaluate Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of PLX-200 in Pediatric Patients with CLN2 Disease (Late-Infantile Neuronal Ceroid Lipofuscinosis) (CLN2 Intervention-Specific Assessment [ISA] Under the PLX-200-600 Master Protocol)
|
PLX-200 will be BID, with equal doses given approximately 12 hours apart, 30 minutes before the morning and evening meals, for 101 weeks (5-week Titration Period and 96-week Maintenance Period) based on each participant's weight.
Dosing will begin with a 5-week TP based on the participant's weight group to achieve a target maintenance dose (TMD).
Ostatní jména:
|
|
Experimentální: PLX-200 (Sandhoff Disease Cohort)
An Open-Label, Multicenter, Phase 2 Study to Evaluate Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of PLX-200 in Pediatric Patients with Sandhoff Disease (GM2 Gangliosidosis Type II) (Sandhoff Disease Intervention-Specific Assessment [ISA] Under the PLX-200-600 Master Protocol)
|
PLX-200 will be BID, with equal doses given approximately 12 hours apart, 30 minutes before the morning and evening meals, for 101 weeks (5-week Titration Period and 96-week Maintenance Period) based on each participant's weight.
Dosing will begin with a 5-week TP based on the participant's weight group to achieve a target maintenance dose (TMD).
Ostatní jména:
|
|
Experimentální: PLX-200 (Krabbe Disease Cohort)
An Open-Label, Multicenter, Phase 2 Study to Evaluate Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of PLX-200 in Pediatric Patients with Krabbe Disease (Globoid Cell Leukodystrophy) (Krabbe Disease Intervention-Specific Assessment [ISA] Under the PLX-200-600 Master Protocol)
|
PLX-200 will be BID, with equal doses given approximately 12 hours apart, 30 minutes before the morning and evening meals, for 101 weeks (5-week Titration Period and 96-week Maintenance Period) based on each participant's weight.
Dosing will begin with a 5-week TP based on the participant's weight group to achieve a target maintenance dose (TMD).
Ostatní jména:
|
Co je měření studie?
Primární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
|
To evaluate the safety and tolerability of PLX-200 in study participants 2 to 15 years old1 with LSDs2 during the treatment period.
Časové okno: Until 30 days after the last administration of the study drug.
|
Incidence and severity of treatment-emergent adverse events (TEAEs) until 30 days after the last administration of the study drug as well as withdrawals due to the TEAEs.
|
Until 30 days after the last administration of the study drug.
|
|
To evaluate the safety and tolerability of PLX-200 in study participants 2 to 15 years old1 with LSDs2 during the treatment period.
Časové okno: 30 days after the last administration of the study drug
|
Incidence and severity of serious adverse events (SAEs) until 30 days after the last administration of the study drug.
|
30 days after the last administration of the study drug
|
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To evaluate the change from baseline in clinical laboratory parameters in study participants 2 to 15 years old with LSDs during the treatment period.
Časové okno: Week 102
|
Week 102
|
|
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To evaluate the change from baseline in physical examination results in study participants 2 to 15 years old with LSDs during the treatment period.
Časové okno: Week 102
|
Week 102
|
|
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To evaluate the change from baseline vital signs in study participants 2 to 15 years old with LSDs during the treatment period.
Časové okno: Week 102
|
Week 102
|
|
|
To evaluate the change from baseline in 12-lead electrocardiogram in study participants 2 to 15 years old with LSDs during the treatment period.
Časové okno: Week 102
|
Week 102
|
Sekundární výstupní opatření
Měření výsledku |
Popis opatření |
Časové okno |
|---|---|---|
|
To evaluate the clinical activity of PLX-200 in study participants 2 to 15 years old with LSDs as measured by each respective instrument as specified in the Intervention Specific Assessment (ISA).
Časové okno: Week 102
|
Week 102
|
|
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Change from Baseline in Vineland Adaptive Behavior Scales, Third Edition (VABS-3) Score
Časové okno: Week 102
|
To evaluate the clinical activity of PLX-200 in pediatric patients with late-infantile Krabbe/Sandhoff/CLN2/CLN3 disease using the Vineland Adaptive Behavior Scales, Third Edition (VABS-3), over 101 weeks of treatment.
|
Week 102
|
|
Caregiver Global Impression of Severity
Časové okno: Week 102
|
To evaluate clinical activity of PLX-200 as reported by the caregiver.
Change from baseline to Week 102 in Caregiver Global Impression of Severity (CaGI-S).
|
Week 102
|
Spolupracovníci a vyšetřovatelé
Zde najdete lidi a organizace zapojené do této studie.
Sponzor
Termíny studijních záznamů
Tato data sledují průběh záznamů studie a předkládání souhrnných výsledků na ClinicalTrials.gov. Záznamy ze studií a hlášené výsledky jsou před zveřejněním na veřejné webové stránce přezkoumány Národní lékařskou knihovnou (NLM), aby se ujistily, že splňují specifické standardy kontroly kvality.
Hlavní termíny studia
Začátek studia (Odhadovaný)
1. prosince 2026
Primární dokončení (Odhadovaný)
31. prosince 2028
Dokončení studie (Odhadovaný)
1. února 2029
Termíny zápisu do studia
První předloženo
17. července 2026
První předloženo, které splnilo kritéria kontroly kvality
28. července 2026
První zveřejněno (Aktuální)
31. července 2026
Aktualizace studijních záznamů
Poslední zveřejněná aktualizace (Aktuální)
31. července 2026
Odeslaná poslední aktualizace, která splnila kritéria kontroly kvality
28. července 2026
Naposledy ověřeno
1. července 2026
Více informací
Termíny související s touto studií
Klíčová slova
Další relevantní podmínky MeSH
- Onemocnění mozku
- Onemocnění centrálního nervového systému
- Nemoci nervového systému
- Metabolismus, vrozené chyby
- Genetické choroby, vrozené
- Metabolické choroby
- Demyelinizační onemocnění
- Poruchy metabolismu lipidů
- Nemoci mozku, metabolické, vrozené
- Nemoci mozku, Metabolické
- Dědičná demyelinizační onemocnění centrálního nervového systému
- Leukoencefalopatie
- Metabolismus lipidů, vrozené chyby
- Lysozomální střádavá onemocnění, nervový systém
- Sfingolipidózy
- Lipidózy
- Gangliosidózy, GM2
- Gangliosidózy
- Vrozené, dědičné a neonatální nemoci a abnormality
- Nutriční a metabolické nemoci
- Lysozomální střádavá onemocnění
- Leukodystrophy, Globoid Cell
- Sandhoffova nemoc
- Organické chemikálie
- Ethers
- Mastné kyseliny
- Lipidy
- Uhlovodíky
- Uhlovodíky, cyklické
- Kyseliny, acyklické
- Karboxylové kyseliny
- Uhlovodíky, aromatické
- Fenoly
- Deriváty benzenu
- Kyseliny pentanoové
- Valerates
- Mastné kyseliny, těkavé
- Butyráty
- Fenyl ethery
- Kyseliny fibrové
- Isobutyrates
- Gemfibrozil
Další identifikační čísla studie
- PLX-200-600
Plán pro data jednotlivých účastníků (IPD)
Plánujete sdílet data jednotlivých účastníků (IPD)?
NE
Informace o lécích a zařízeních, studijní dokumenty
Studuje lékový produkt regulovaný americkým FDA
Ano
Studuje produkt zařízení regulovaný americkým úřadem FDA
Ne
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