CClinicalTrials.gg
WithdrawnNCT05361447Updated Mar 6, 2025

Diazepam Trial in GAD65 Associated Epilepsy

A Phase 1/2 interventional study of Diazepam in GAD 65 Antibody-associated Epilepsy, sponsored by Mayo Clinic. Withdrawn at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-03-06.

Sponsored by Mayo Clinic · Phase 1/2, Interventional, and Treatment

Why this study was withdrawn
Study population was difficult to identify for enrollment interest.
Phase
Phase 1/2
Study type
Interventional
Enrollment
0
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

The purpose of this study is to determine whether diazepam reduces the frequency of seizures in GAD65 antibody associated epilepsy.

Read the detailed description

GAD65 is an intracellular enzyme that plays a key role in the conversion of glutamate to gamma-aminobutyric acid (GABA), the primary inhibitory neurotransmitter in the CNS. Benzodiazepines augment the sensitivity of the GABA-A receptor to GABA, prolonging its inhibitory effect, perhaps enhancing the potential for neural inhibition in conditions in which GABA is depleted.

GAD65 antibodies have been identified in a subset of patients with drug resistant focal epilepsy and limbic encephalitis. While it has not been definitively determined that these antibodies cause GAD65 inhibition and GABA depletion directly, diazepam, a common benzodiazepine, has been established as a mainstay of therapy for stiffperson's syndrome, a condition that is commonly associated with GAD65 antibody positivity. Given these observations, diazepam has been used by the investigators in a small number of patients with intractable epilepsy in the setting of GAD65 antibody positivity, with some encouraging anecdotal results with one patient being rendered seizure free for three years.

The purpose of this study is to generate prospective data on use of diazepam in patients with epilepsy related to high-titer GAD65 antibody positivity.

02

Conditions studied

  • GAD 65 Antibody-associated Epilepsy

Browse trials for

03

In context

Epilepsy

1,805 studies on the registry are indexed under Epilepsy; 417 are open to participants now.

Browse Epilepsy studies →

Lead sponsor

Mayo Clinic is the lead sponsor of 3,218 studies on the registry; 670 are open to participants now.

Of its 445 completed or terminated interventional studies of FDA-regulated products, 313 (70%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • High-titer serum GAD65 positivity > 20 nmol/L High-titer serum GAD65 IgG seropositivity titer >20 nmol/L and/or CSF GAD65 seropositivity titer > 0.02 nmol/L.
  • Drug-resistant focal epilepsy, having failed 2 previous anti-seizure medications.
  • Stable treatment for the 1 month prior to enrollment.
  • Patients must be able to give informed consent or have an appropriate representative available to do.

Exclusion criteria

Exclusion Criteria:

  • Alternative etiology for epilepsy.
  • Already on another benzodiazepine.
  • On a regularly scheduled opiate.
  • Co-existing antibodies associated with seizures.
  • Pregnancy or breast feeding.
05

Study design

Phase
Phase 1 / Phase 2
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
0 participants (actual)

Study arms

  • Experimental
    GAD65 Associated Epilepsy

    Subjects diagnosed with GAD65 associated epilepsy, serum high-titer GAD65 positivity, trialed and failed at least 2 anti-seizure medications, at least 4 seizures per month will be started on diazepam.

    Drug: Diazepam

Interventions

  • DrugDiazepam

    5 mg twice daily oral for 1 week and then increase to 10 mg twice daily oral

    Also known as: Valium

06

What researchers measure

Primary outcomes

  1. Change in seizure frequency

    Median percentage change in the mean monthly frequency of seizures as measured by patient recorded seizure frequency

    Time frame: Baseline, 3 months

07

Study locations

1 site
  • Mayo Clinic in Rochester
    Rochester, Minnesota 55905, United States
08

References and documents

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 6, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05361447
Lead sponsor
Mayo Clinic
Responsible party
Kelsey M. Smith (Principal Investigator, Mayo Clinic) — Principal investigator
First posted
May 4, 2022
Start date
Jan 11, 2023
Primary completion
Dec 13, 2024
Completion
Dec 13, 2024
Last update
Mar 6, 2025

Study contacts

Kelsey Smith, MD
principal investigator · Mayo Clinic

Oversight

Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is withdrawn, as verified in Mar 2025. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion