Anti-Epilepsy Medication Valproate Administered Via ICV Route and Catheters and Pumps for CSF Infusion

NCT04529954 · Status: TERMINATED · Phase: PHASE1/PHASE2 · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2024-03-13

No results posted yet for this study

Summary

This is a non-randomized open-label extension study for subjects having completed protocol DA071976 or CLN100P.01.

Conditions

  • Focal Epilepsy

Interventions

DRUG

Valproic Acid delivered to ICV

Valproic Acid delivered to ICV via an implantable pump and catheter system

Sponsors & Collaborators

  • Cerebral Therapeutics LLC

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-01-01
Primary Completion
2024-03-01
Completion
2024-03-01

Countries

  • Australia
  • Israel

Study Locations

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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 NCT04529954 on ClinicalTrials.gov