Ganaxolone Expanded Access Program Compassionate Use

NCT04678479 · Status: NO_LONGER_AVAILABLE · Type: EXPANDED_ACCESS

Last updated 2024-01-22

No results posted yet for this study

Summary

The primary objective is to provide GNX to patients ≥ 2 years with CDD-related seizures who are refractory to, or intolerant of, standard therapy.

Conditions

  • CDKL5 Disorder

Interventions

DRUG

Ganaxolone

ganaxolone

Sponsors & Collaborators

  • Marinus Pharmaceuticals

    lead INDUSTRY

Principal Investigators

  • Paula Bokesch, MD, FAAP · Marinus Pharmaceuticals, Inc.

  • Igor Grachev, MD, PhD · Marinus Pharmaceuticals, Inc.

Eligibility

Min Age
2 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04678479 on ClinicalTrials.gov