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NMDA Receptor Antagonist

Study drug-dextromethorphan (DM) for Rett Syndrome (PCTDMRTT Trial)

Phase 2
Waitlist Available
Led By Sakkubai R Naidu, MD
Research Sponsored by Hugo W. Moser Research Institute at Kennedy Krieger, Inc.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be younger than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up initial evaluation and at the end of the 3 month study. the test lasts 45 minutes
Awards & highlights

Summary

Dr. Sakkubai Naidu, Principal Investigator, is initiating a double blinded placebo controlled clinical drug trial using dextromethorphan (DM) in Rett Syndrome (RTT), at the Pediatric Clinical Research Unit (PCRU) of the Johns Hopkins Hospital/Kennedy Krieger Institute. Funding source , FDA-00PD It has been shown that receptors for a certain brain chemical called glutamate, in particular the NMDA type, are increased in the brain of young RTT patients (\<10 years of age). This chemical and its receptors, when in excess, cause harmful over-stimulation of nerve cells in the brain, contributing in part to the seizures, behavioral problems, and learning disabilities in RTT. The investigators propose to initiate a specific treatment using DM to counter/block the effects of this brain chemical and its excessive receptors to improve the ill effects of increased glutamate/NMDA receptors, because of DM's identified ability to block NMDA receptors. DM is available for human consumption. Infants and children with respiratory infections and cough, as well as non-ketotic hyperglycinemia, are treated with DM, which has been well tolerated.

Eligible Conditions
  • Rett Syndrome

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~initial evaluation and at the end of the 3 month study. the test lasts 45 minutes
This trial's timeline: 3 weeks for screening, Varies for treatment, and initial evaluation and at the end of the 3 month study. the test lasts 45 minutes for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Change in Mullen, Expressive Language Sub-scale Scores, Pre- and Post-Intervention
Change in Mullen; Fine Motor Sub-scale Scores, Pre- and Post-Intervention
Change in Mullen; Receptive Language Subscale Scores, Pre- and Post-Intervention
+1 more
Secondary outcome measures
Change in Ghuman-Folstein Screen for Social Interaction (SSI) Score, Pre- and Post-Intervention.
Change in Rett Syndrome Behavior Questionnaire Score, Pre- and Post-Intervention
Change in VABS: Motor Skills Domain Scores, Pre- and Post-Intervention
+3 more
Other outcome measures
Change in PedsQL Emotional Functioning Subscale Score, Pre- and Post-Intervention
Change in PedsQL Physical Functioning Subscale Score, Pre- and Post-Intervention
Change in PedsQL School Functioning Subscale Score, Pre- and Post-Intervention
+4 more

Trial Design

2Treatment groups
Active Control
Placebo Group
Group I: Study drug-dextromethorphan (DM)Active Control1 Intervention
MECP2 mutation positive subjects randomized to receive DM
Group II: Placebo groupPlacebo Group1 Intervention
MECP2 positive subjects randomized to the placebo compound

Find a Location

Who is running the clinical trial?

Hugo W. Moser Research Institute at Kennedy Krieger, Inc.Lead Sponsor
88 Previous Clinical Trials
24,890 Total Patients Enrolled
2 Trials studying Rett Syndrome
3,038 Patients Enrolled for Rett Syndrome
The Johns Hopkins Institute for Clinical and Translational Research (ICTR)UNKNOWN
Sakkubai R Naidu, MDPrincipal InvestigatorThe Kennedy Krieger Institute and Johns Hopkins SOM
~4 spots leftby Sep 2025