- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT07740512
Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of PLX-200 in Pediatric Patients (Master Protocol)
28. Juli 2026 aktualisiert von: 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.
Studienübersicht
Status
Noch keine Rekrutierung
Intervention / Behandlung
Detaillierte Beschreibung
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.
Studientyp
Interventionell
Einschreibung (Geschätzt)
24
Phase
- Phase 2
Kontakte und Standorte
Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.
Studienkontakt
- Name: Minsu Kang, PhD
- Telefonnummer: 217-779-7736
- E-Mail: minsukang@polaryx.com
Teilnahmekriterien
Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.
Zulassungskriterien
Studienberechtigtes Alter
- Kind
Akzeptiert gesunde Freiwillige
Nein
Beschreibung
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.
Studienplan
Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Nicht randomisiert
- Interventionsmodell: Einzelgruppenzuweisung
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Experimental: 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).
Andere Namen:
|
|
Experimental: 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).
Andere Namen:
|
|
Experimental: 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).
Andere Namen:
|
|
Experimental: 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).
Andere Namen:
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
To evaluate the safety and tolerability of PLX-200 in study participants 2 to 15 years old1 with LSDs2 during the treatment period.
Zeitfenster: 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.
Zeitfenster: 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
|
|
To evaluate the change from baseline in clinical laboratory parameters in study participants 2 to 15 years old with LSDs during the treatment period.
Zeitfenster: 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.
Zeitfenster: 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.
Zeitfenster: 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.
Zeitfenster: Week 102
|
Week 102
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
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).
Zeitfenster: Week 102
|
Week 102
|
|
|
Change from Baseline in Vineland Adaptive Behavior Scales, Third Edition (VABS-3) Score
Zeitfenster: 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
Zeitfenster: 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
|
Mitarbeiter und Ermittler
Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.
Sponsor
Studienaufzeichnungsdaten
Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.
Haupttermine studieren
Studienbeginn (Geschätzt)
1. Dezember 2026
Primärer Abschluss (Geschätzt)
31. Dezember 2028
Studienabschluss (Geschätzt)
1. Februar 2029
Studienanmeldedaten
Zuerst eingereicht
17. Juli 2026
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
28. Juli 2026
Zuerst gepostet (Tatsächlich)
31. Juli 2026
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
31. Juli 2026
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
28. Juli 2026
Zuletzt verifiziert
1. Juli 2026
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
- Erkrankungen des Gehirns
- Erkrankungen des zentralen Nervensystems
- Erkrankungen des Nervensystems
- Stoffwechsel, angeborene Fehler
- Genetische Krankheiten, angeboren
- Stoffwechselerkrankungen
- Demyelinisierende Krankheiten
- Störungen des Fettstoffwechsels
- Gehirnerkrankungen, Stoffwechselerkrankungen, angeboren
- Gehirnerkrankungen, Stoffwechsel
- Erbliche Demyelinisierungskrankheiten des Zentralnervensystems
- Leukenzephalopathien
- Fettstoffwechsel, angeborene Fehler
- Lysosomale Speicherkrankheiten, Nervensystem
- Sphingolipidosen
- Lipidosen
- Gangliosidosen, GM2
- Gangliosidosen
- Angeborene, erbliche und neonatale Krankheiten und Anomalien
- Ernährungs- und Stoffwechselerkrankungen
- Lysosomale Speicherkrankheiten
- Leukodystrophie, Globoidzelle
- Sandhoff-Krankheit
- Organische Chemikalien
- Ethers
- Fettsäuren
- Lipide
- Kohlenwasserstoffe
- Kohlenwasserstoffe, zyklisch
- Säuren, acyclisch
- Carboxylsäuren
- Kohlenwasserstoffe, aromatisch
- Phenole
- Benzolderivate
- Pentansäure
- Valerates
- Fettsäuren, flüchtig
- Butyate
- Phenylether
- Fibrikäuren
- Isobutyate
- Gemfibrozil
Andere Studien-ID-Nummern
- PLX-200-600
Plan für individuelle Teilnehmerdaten (IPD)
Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?
NEIN
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Ja
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
Nein
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