Double-blind, Randomized, Placebo-controlled Trial of Ganaxolone in CDKL5 Deficiency Patients 6 Months to Less Than 2 Years Old

Immedica Pharma AB

Status and phase: Begins enrollment in 3 months; Phase 3

Conditions: CDKL5 Deficiency Disorder

Treatments: Drug: Placebo; Drug: Ganaxolone

Study type: Interventional

Funder types: Industry

Identifiers

NCT05249556

1042-CDD-3002

Details and patient eligibility

About

This study will assess the efficacy, safety, and tolerability of ganaxolone (GNX) compared with placebo (PBO) as adjunctive therapy to the participant's standard anti-epileptic medication for the treatment of seizures in pediatric patients from 6 months to less than 2 years old with genetically confirmed CDD during a 12-week, DB phase. Pharmacokinetic (PK) assessments and population PK analyses will also be performed during this time. The DB phase will be followed by an optional long-term OL phase at which time all participants will receive GNX as an adjunct to their standard anti-seizure medication. Efficacy, safety and tolerability, and PK assessments will continue to be performed.

Enrollment: 20 estimated patients

Sex: All

Ages: 6 months to 2 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. A diagnosis of CDD, including molecular confirmation of a pathogenic or likely pathogenic CDKL5 variant and refractory seizures (see Inclusion criterion 5).

   1. The principal investigator (PI) must review the results of the genetic analysis and confirm that gene mutation is likely to be the cause of the epilepsy syndrome.
   2. If the participant has a de novo variant of unknown significance (VUS) in the kinase domain of the CDKL5 gene, parental testing is negative and meets all other inclusion criteria, then the participant can be included.
   3. Genetic mutations will be confirmed by the sponsor's chosen central laboratory. In France, genetic mutations may be confirmed by an approved French organization, in compliance with French legislation prior to Screening/Visit 1.

2. Male or female participants aged 6 months to less than 2 years.

3. Parent(s) or LAR willing to give written informed consent, after being properly informed of the nature and risks of the study and prior to engaging in any study-related procedures.

4. Failure to control seizures despite appropriate trial of 1 or more anti-seizure medications at therapeutic doses.

5. Have a history of at least 8 countable seizures during the 28 days prior to screening. Countable seizures will be defined by the following:

   1. Seizures with or without impairment of consciousness with a clear motor component, including generalized tonic-clonic, focal to bilateral tonic-clonic, atonic, bilateral clonic, bilateral tonic, focal motor seizures with or without impaired awareness, or infantile spasms. Clusters of infantile spasms/tonic seizures will be counted as a single seizure.
   2. Excludes myoclonic, absence or focal aware seizures without a clear motor component.

6. Participants should be on a stable regimen of anti-seizure medications for ≥ 2 weeks prior to the screening visit, without a foreseeable change in dosing for the duration of the DB phase.

   1. Concurrent use of adrenocorticotropic hormone (ACTH), prednisone or other glucocorticoids or vigabatrin are permitted.
   2. Vagus nerve stimulator (VNS) settings, ketogenic diet, or a modified Atkins diet should be unchanged for 1 month prior to screening and throughout the study (until the end of the DB phase).

7. Use of dietary supplements or herbal preparations is permitted if the participant has been using them consistently for more than 1 month prior to screening and there is no plan on changing the dose for the duration of the DB phase.

8. Parent/caregiver is able and willing to maintain an accurate and complete daily seizure eDiary for the duration of the study.

9. Able and willing to administer IP with food 3 times daily.

Exclusion criteria

1. Have an active CNS infection, demyelinating disease, degenerative neurological disease, or CNS disease deemed progressive as evaluated by brain imaging (magnetic resonance imaging [MRI]).
2. Have any disease or condition (medical or surgical; other than CDKL5 deficiency) at screening 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 IP, or would place the participant at increased risk.
3. Has a positive result for tetrahydrocannabinol (THC) test (via urine or plasma drug screen) at the screening visit. Concomitant Epidiolex/Epidyolex (cannabidiol derivative [CBD]) use will be allowed in the DB phase provided the participant has been on a stable dose for at least 1 month prior to screening and is expected to remain on a stable dose without a foreseeable change for the duration of the DB phase.
4. Use of a CBD preparation other than Epidiolex/Epidyolex for 1 month prior to screening.
5. An AST (aspartate aminotransferase/serum glutamic-oxaloacetic transaminase [SGOT]) or ALT (alanine aminotransferase/serum glutamic-pyruvic transaminase [SGPT]) > 3 times the upper limit of normal (ULN) at study entry. If AST or ALT increases > 3 X ULN during the study, the participant should be followed with weekly laboratory repeat testing and continue in study if levels trending down. The participant will be discontinued if levels do not decline to < 3 X ULN.
6. Total bilirubin levels greater than the ULN at study entry. In cases of a documented, stable medical condition (ie, Gilbert's Syndrome) resulting in levels of total bilirubin greater than the ULN, the medical monitor can determine if a protocol exception can be made. If total bilirubin increases to 1.5 x the ULN or more during study, the participant will be discontinued.
7. Participants with significant renal insufficiency, with an estimated glomerular filtration rate (eGFR) < 30 mL/min (calculated using the Cockcroft-Gault formula or Pediatric GFR calculator or Bedside Schwartz).
8. Using St. John's Wort.
9. Have been exposed to any other investigational drug within 30 days or less than 5 half-lives prior to screening.
10. Known allergic reaction or sensitivity to GNX or its excipients.
11. Participating in any other study involving administration of an investigational medication or device.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Triple Blind

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20 participants in 2 patient groups, including a placebo group

GNX

Experimental group

Description:

The suspension contains GNX (50 mg/mL), hydroxypropyl methylcellulose, polyvinyl alcohol, sodium lauryl sulfate, simethicone, methylparaben, propylparaben, citric acid, and sodium citrate at pH 3.5 to 4.2, and is sweetened with sucralose and flavored with artificial cherry.

Treatment:

Drug: Ganaxolone

Placebo

Placebo Comparator group

Description:

The PBO suspension consists of titanium dioxide, Avicel® (microcrystalline cellulose and carboxymethylcellulose sodium), sodium lauryl sulfate, simethicone, methylparaben, propylparaben, citric acid, sodium citrate and is sweetened with sucralose and flavored with artificial cherry

Treatment:

Drug: Placebo