Clinical Trials Directory

Trials / Completed

CompletedNCT00441896

A Randomized, Controlled Trial of Ganaxolone in Patients With Infantile Spasms

A Double-blind, Placebo-controlled, Dose-ranging Clinical Study to Evaluate the Safety, Tolerability, and Antiepileptic Activity of Ganaxolone in Treatment of Patients With Infantile Spasms

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
57 (actual)
Sponsor
Marinus Pharmaceuticals · Industry
Sex
All
Age
4 Months – 24 Months
Healthy volunteers
Not accepted

Summary

The study consists of cohorts where participants are randomized, in a 2:1 ratio, to 1 of 2 sequences, A and B. In each cohort, Sequence A, comprised of participants, who will receive ascending doses of ganaxolone and ascending doses of placebo. Sequence B, comprised of participants, who will receive ascending doses of placebo and ascending doses of ganaxolone. The dosing level in each subsequent cohort will be based upon experience gained from previous cohorts.

Detailed description

Male or female, 4 to 24 months of age (inclusive) with a diagnosis of IS with a 24 hour video EEG (vEEG) recording confirming the diagnosis and previously treated with 3 or fewer antiepileptic drugs (AEDs) are eligible for the study. The subject is able to continue treatment with concomitant AEDs (no more than 2; adrenocorticotropic hormone \[ACTH\], corticosteroids, felbamate, and vigabatrin are not allowed concomitantly). A ketogenic diet is permitted if it can be maintained for the duration of the study. There will be a total of three weekly 24-hr video EEGs (baseline, end of weeks 1 and 2 of treatment). Dosing titration begins the day after each video EEG during the inpatient stay. All subjects will be receiving ganaxolone the day after the second video EEG. A Data Monitoring Board (DMB) will determine whether successive cohorts of subjects can be dosed at an increased dose level; up to a maximum of 6 cohorts.

Conditions

Interventions

TypeNameDescription
DRUGGanaxolone
OTHERPlacebo

Timeline

Start date
2007-01-01
Primary completion
2008-05-01
Completion
2008-05-01
First posted
2007-03-01
Last updated
2023-06-02
Results posted
2023-06-02

Locations

15 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00441896. Inclusion in this directory is not an endorsement.