- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT05249556
Open-label, Single-arm Trial of Ganaxolone in CDD Patients 6 Months to Less Than 2 Years Old
An Open-label, Single-arm, 52-week, Multicenter Phase 3 Trial to Assess Pharmacokinetics, Safety, Tolerability, and Activity of Adjunctive Ganaxolone for the Treatment of Seizures Associated With Genetically Confirmed Cyclin-dependent Kinase-like 5 (CDKL5) Deficiency Disorder (CDD) in Pediatric Patients From 6 Months to Less Than 2 Years of Age
The goal of this clinical trial is to learn how patients with CDKL-5 deficiency disorder (CDD) aged 6 months to 2 years of age respond to treatment with ganaxolone. The main questions the trial aims to answer are:
- The amount of the medicine that was in participants' bodies and the safety of the medicine.
- Does the medicine ganaxolone lower the number of seizures when used in addition to the participant's usual anti-seizure treatment.
Participants will:
Take ganaxolone 3 times daily for up to 52 weeks. Visit the clinic every 3 to 5 weeks for the initial 17 weeks of the trial and thereafter every 11 to 12 weeks.
The participant's caregiver will:
Keep a daily diary of the participants seizures and use of anti-seizure medications, including the trial drug ganaxolone.
Studieoversikt
Status
Forhold
Intervensjon / Behandling
Detaljert beskrivelse
This is an open-label, single-arm, 52-week, multicenter trial of adjunctive ganaxolone treatment in participants 6 months to less than 2 years of age with genetically confirmed CDD. The trial consists of an up to 2-week Screening Period, 4-week prospective Baseline Period, followed by 2 parts: Part A; a 17-week ganaxolone treatment phase (including 4 to 5 weeks of ganaxolone titration followed by 12 to 13 weeks of dose maintenance) and Part B; a 35-week ganaxolone maintenance phase, and a 2-week taper period at the end of the trial. Tapering will not apply for participants continuing ganaxolone treatment after the trial.
The Screening Period will follow the Screening Visit to ensure caregivers can classify seizures and comply with completion instructions of an electronic seizure and medication diary. This will be followed by a 4-week prospective Baseline Period to assess seizure frequency for trial eligibility.
Up to 15 participants will be enrolled to ensure at least 12 participants are evaluable for the primary PK endpoints at the end of Part A of the trial, including at least 3 participants experiencing uncontrolled seizures despite treatment with at least 2 anti-seizure medications.
Participants will be monitored at Baseline and at specified visits to assess the exposure, safety and tolerability and activity of ganaxolone. PK samples will be collected at specified timepoints up until completion of Part A.
Clinical laboratory testing will be performed at local laboratories at participating sites.
Studietype
Registrering (Antatt)
Fase
- Fase 3
Kontakter og plasseringer
Studiekontakt
- Navn: Clinical Project Manager
- Telefonnummer: +46 8 533 39 500
- E-post: clinical@immedica.com
Studer Kontakt Backup
- Navn: Clinical Project Manager
- E-post: clinical@immedica.com
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
Key Inclusion Criteria:
-
A diagnosis of CDD, including molecular confirmation of a pathogenic or likely pathogenic CDKL5 variant.
-
Male or female participants aged 6 months to less than 2 years at the Baseline Visit.
-
Failure to control seizures despite appropriate use of 1 or more anti-seizure medications at therapeutic doses. At least 3 participants will be included who failed to control seizures despite appropriate use of at least 2 anti-seizure medications.
-
Participants will have refractory seizures with a history of at least 8 countable seizures of primary seizure types during the 28 days prospective Baseline Period prior to the Baseline Visit. Primary seizure types are seizures with or without impairment of consciousness with a clear motor component, including generalized tonic-clonic, focal to bilateral tonic-clonic, atonic/drop, bilateral clonic, bilateral tonic (sustained motor activity ≥ 3 seconds). Clusters of uncountable seizures will be counted as a single seizure.
- Primary seizures exclude epileptic spasms. Patients with epileptic spasms are eligible for enrolment but epileptic spasms will not be counted as qualifying countable seizures for eligibility. Epileptic spasms should not constitute the dominant seizure type during the Baseline Period.
- Primary seizures exclude myoclonic, absence, generalized non-motor seizures, and focal motor or non-motor seizures with or without impairment of awareness.
-
Participants should be receiving a stable regimen of anti-seizure medications at Screening through to the end of the 4-week prospective Baseline Period and have no foreseeable change for the duration of Part A.
- Concurrent use of adrenocorticotropic hormone, prednisone, other glucocorticoids, or vigabatrin are permitted.
- Vagus nerve stimulator (VNS) settings, ketogenic diet, or a modified Atkins diet should be unchanged for 1 month prior to the Screening Visit, throughout the Screening Period and the 4-week prospective Baseline Period and without foreseeable change for the duration of Part A at the time of the Baseline Visit.
-
Parent/caregiver is able and willing to maintain an accurate and complete daily seizure diary for the duration of the trial.
Key Exclusion Criteria:
- Have an active CNS infection, demyelinating disease, degenerative neurological disease, or CNS disease deemed progressive as evaluated by brain imaging (magnetic resonance imaging).
- Have any disease or condition (medical or surgical; other than CDKL5 deficiency) that might compromise the hematologic, cardiovascular, pulmonary, renal, gastrointestinal, or hepatic systems; or other conditions that might interfere with the absorption, distribution, metabolism, or excretion of the investigational product or would place the participant at increased risk.
- History of or present AST (aspartate aminotransferase/serum glutamic-oxaloacetic transaminase) or ALT (alanine aminotransferase/serum glutamic-pyruvic transaminase) >3 times the upper limit of normal (ULN) at Baseline and confirmed by a repeat testing.
- History of or present total bilirubin levels greater than the ULN at trial Baseline and confirmed by a repeat testing. In cases of a documented, stable medical condition (i.e., Gilbert's Syndrome) resulting in levels of total bilirubin greater than the ULN, the Medical Monitor will determine if an exception can be made.
- Participants with significant renal insufficiency, with an estimated glomerular filtration rate (eGFR) <30 mL/min (calculated using the Cockcroft-Gault formula or Pediatric eGFR calculator or Bedside Schwartz).
- Regular use of St. John's Wort or strong CYP3A4 inducers, e.g., phenytoin, carbamazepine or phenobarbital (N.B. phenytoin and phenobarbital are permitted as rescue medication on as-need basis but are not permitted as continuous maintenance medication).
- Have been exposed to any other investigational drug within 30 days or less than its 5 half-lives prior to the Screening Visit.
- Previous treatment with ganaxolone.
- Participation in any other trial involving administration of an investigational medication or device.
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: Ganaxolone
Ganaxolone sodium benzoate-free oral suspension 50 mg/ml |
Ganaxolone
Andre navn:
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Ganaxolone exposure in participants receiving ganaxolone doses up to 63 mg/kg/day
Tidsramme: Baseline through 17 weeks
|
Pharmacokinetic (PK) exposure parameter derived from population PK modelling and simulation: steady-state maximum concentration (Cmax,ss) |
Baseline through 17 weeks
|
|
Ganaxolone exposure in participants receiving ganaxolone doses up to 63 mg/kg/day
Tidsramme: Baseline through 17 weeks
|
PK exposure parameter derived from population PK modelling and simulation: trough concentration (Ctrough) |
Baseline through 17 weeks
|
|
Ganaxolone exposure in participants receiving ganaxolone doses up to 63 mg/kg/day
Tidsramme: Baseline through 17 weeks
|
PK exposure parameter derived from population PK modelling and simulation: systemic exposure (Caverage,ss derived as AUC over a dosing interval / tau) |
Baseline through 17 weeks
|
|
Safety and tolerability of ganaxolone as adjunctive therapy for the treatment of seizures in participants receiving ganaxolone doses up to 63 mg/kg/day
Tidsramme: Baseline through to 52 weeks
|
Frequency, type, and severity of adverse events (AEs) |
Baseline through to 52 weeks
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
|
Ganaxolone PK parameters at steady-state in participants receiving ganaxolone doses up to 63 mg/kg/day.
Tidsramme: Baseline through to 17 weeks
|
Non-compartmental-like steady-state PK parameters derived from population PK modelling and simulation: steady-state time to maximum concentration (tmax,ss) |
Baseline through to 17 weeks
|
|
Ganaxolone PK parameters at steady-state in participants receiving ganaxolone doses up to 63 mg/kg/day.
Tidsramme: Baseline through to 17 weeks
|
Non-compartmental-like steady-state PK parameters derived from population PK modelling and simulation: exposure accumulation ratios |
Baseline through to 17 weeks
|
|
Ganaxolone PK parameters at steady-state in participants receiving ganaxolone doses up to 63 mg/kg/day.
Tidsramme: Baseline through to 17 weeks
|
Non-compartmental-like steady-state PK parameters derived from population PK modelling and simulation: swing [(Cmax-Cmin)/Cmin]) |
Baseline through to 17 weeks
|
|
Activity of ganaxolone as adjunctive therapy for the treatment of primary seizures at the end of the 17-week treatment period (Part A)
Tidsramme: Baseline through to 17 weeks
|
Percent change from baseline in 28-day primary seizure frequency during the treatment period relative to the 4-week prospective Baseline Phase |
Baseline through to 17 weeks
|
|
Activity of ganaxolone as adjunctive therapy for the treatment of primary seizures at the end of the 17-week treatment period (Part A)
Tidsramme: Baseline through to 17 weeks
|
Percentage of participants experiencing ≥50% reduction in the 28-day primary seizure frequency compared to the 4-week baseline |
Baseline through to 17 weeks
|
|
Activity of ganaxolone as adjunctive therapy for the treatment of primary seizures at the end of the 17-week treatment period (Part A)
Tidsramme: Baseline through to 17 weeks
|
Percent change in seizures by primary seizure type |
Baseline through to 17 weeks
|
|
Activity of ganaxolone as adjunctive therapy for the treatment of primary seizures at the end of the 17-week treatment period (Part A)
Tidsramme: Baseline through to 17 weeks
|
Percent change in primary seizure-free days |
Baseline through to 17 weeks
|
|
Activity of ganaxolone as adjunctive therapy for the treatment of primary seizures at the end of the 17-week treatment period (Part A)
Tidsramme: Baseline through to 17 weeks
|
Clinical Global Impression of Improvement (CGI-I); 7-point Likert scale, higher scores mean a worse outcome |
Baseline through to 17 weeks
|
|
Activity of ganaxolone as adjunctive therapy for the treatment of primary seizures at the end of the 17-week treatment period (Part A)
Tidsramme: Baseline through to 17 weeks
|
Caregiver Global Impression of Change in Seizure Intensity/Duration (CGI-CSID); 7-point Likert scale, higher scores mean a worse outcome |
Baseline through to 17 weeks
|
|
Activity of ganaxolone as adjunctive therapy for the treatment of primary seizures at the end of the 52-week treatment period (Part B)
Tidsramme: Baseline through to 52 weeks
|
Percent change from baseline in 28-day primary seizure frequency during the treatment period relative to the 4-week prospective Baseline Phase |
Baseline through to 52 weeks
|
|
Activity of ganaxolone as adjunctive therapy for the treatment of primary seizures at the end of the 52-week treatment period (Part B)
Tidsramme: Baseline through to 52 weeks
|
Percentage of participants experiencing ≥50% reduction in the 28-day primary seizure frequency compared to the 4-week baseline |
Baseline through to 52 weeks
|
|
Activity of ganaxolone as adjunctive therapy for the treatment of primary seizures at the end of the 52-week treatment period (Part B)
Tidsramme: Baseline through to 52 weeks
|
Percent change in seizures by primary seizure type |
Baseline through to 52 weeks
|
|
Activity of ganaxolone as adjunctive therapy for the treatment of primary seizures at the end of the 52-week treatment period (Part B)
Tidsramme: Baseline through to 52 weeks
|
Percent change in primary seizure-free days |
Baseline through to 52 weeks
|
|
Activity of ganaxolone as adjunctive therapy for the treatment of primary seizures at the end of the 52-week treatment period (Part B)
Tidsramme: Baseline through to 52 weeks
|
Clinical Global Impression of Improvement (CGI-I); 7-point Likert scale, higher scores mean a worse outcome |
Baseline through to 52 weeks
|
|
Activity of ganaxolone as adjunctive therapy for the treatment of primary seizures at the end of the 52-week treatment period (Part B)
Tidsramme: Baseline through to 52 weeks
|
Caregiver Global Impression of Change in Seizure Intensity/Duration (CGI-CSID); 7-point Likert scale, higher scores mean a worse outcome |
Baseline through to 52 weeks
|
Samarbeidspartnere og etterforskere
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Publikasjoner og nyttige lenker
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
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- 1042-CDD-3002
- 2026-528611-26-00 (Ctis)
Plan for individuelle deltakerdata (IPD)
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