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Phase 3 Completed N=326 Randomized Quadruple-blind Treatment

Safety and Efficacy of AVP-923 in PBA Patients With ALS or MS

Pseudobulbar Affect (PBA)
Source: ClinicalTrials.gov NCT00573443 ↗
Enrolled (actual)
326
Serious AEs
7.1%
Results posted
Jul 2013
Primary outcomePrimary: PBA Episode Rate Ratio (Post/Pre), Regression Adjusted — 0.247; 0.237; 0.465 Unit-free (ratio of episodes/week) — p=<0.0001

Summary

Objectives of the study are to evaluate the safety, tolerability, and efficacy of two different doses of AVP-923 (capsules containing either 30 mg of dextromethorphan hydrobromide and 10 mg of quinidine sulfate [AVP-923-30] or 20 mg of dextromethorphan hydrobromide and 10 mg of quinidine sulfate [AVP-923-20]) when compared to placebo, for the treatment of PBA in a population of patients with amyotrophic lateral sclerosis (ALS) or multiple sclerosis (MS) over a 12-week period. An additional objective is to determine the pharmacokinetic parameters of the two different doses of AVP-923 in a subset of the study population. Pseudobulbar Affect (PBA) is a condition characterized by involuntary, sudden and frequent episodes of laughing and/or crying out of proportion or incongruous to the underlying emotion of happiness or sadness Other terms used to describe this condition include emotional lability, emotionalism, emotional incontinence, emotional discontrol, excessive emotionalism, and pathological laughing and crying. The outbursts can occur spontaneously or in response to provocative stimuli such as questions or events. A body of evidence suggests that PBA can be modulated through pharmacologic intervention. Dextromethorphan (DM) is a low-affinity uncompetitive antagonist of the N-Methyl-D-aspartate (NMDA) receptor, reducing the level of excitatory activity. DM also acts at the phencyclidine-binding site, which is part of the NMDA receptor complex. DM is a sigma receptor agonist, suppressing the release of excitatory neurotransmitters. Quinidine (Q) is a known potent inhibitor of cytochrome P450 2D6 (CYP2D6), that decreases the metabolism of dextromethorphan and helps to achieve sustained and therapeutic levels of this drug.

Outcome Measures

OutcomeResultp-value
PRIMARY
PBA Episode Rate Ratio (Post/Pre), Regression Adjusted
0.247; 0.237; 0.465 <0.0001 sig
SECONDARY
Mean Change From Baseline in CNS-LS Total Score by Visit
-6.77; -6.27; -4.58; -8.03; -7.62; -5.70
SECONDARY
Mean Change From Baseline to Day 84 in Neuropsychiatric Inventory (NPI-Q) Frequency and Severity Score (EE Population)
-1.68; -3.09; -1.25; -0.80; -1.81; -0.91
SECONDARY
Mean Change From Baseline to Day 84 in Neuropsychiatric Inventory (NPI-Q) Frequency and Severity Score (ITT Population)
-1.62; -2.56; -1.33; -0.74; -1.59; -0.98
SECONDARY
Mean Change From Baseline at Day 84 in SF-36 (Short-Form) Health Survey Medical Outcome Score by Category
-0.90; -5.30; -4.05; 3.47; -4.26; -1.75
SECONDARY
Mean Change From Baseline at Day 84 in Beck Depression Inventory (BDI-II) Total Score
-1.59; -1.03; -0.02
SECONDARY
Mean Change From Baseline to Day 84 in Pain Rating Scale (PRS) of MS Subjects
-1.0; -0.7; -0.4

Eligibility Criteria

Main Inclusion Criteria:

  • The patient has a diagnosis of Amyotrophic Lateral Sclerosis (according to El Escorial Criteria, WFN, 1998) and the time from diagnosis of ALS is not be longer than 30 months, or the patient has a diagnosis of multiple sclerosis or probable multiple sclerosis (according to McDonald criteria, 2001)
  • The patient has a clinical history and clinical relevant symptoms of Pseudobulbar Affect (PBA)
  • CNS-LS score at baseline is 13 or greater

Main Exclusion Criteria:

  • Patients with myasthenia gravis
  • Any personal history of complete heart block, QTc prolongation, or torsades de pointes
  • Any family history of congenital QT interval prolongation syndrome
  • Patients with known sensitivity to quinidine, dextromethorphan or opiate drugs (codeine, etc.)
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00573443). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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