Fasoracetam in adolescents with ADHD and glutamatergic gene network variants disrupting mGluR neurotransmitter signaling
Фазорацетам у подростков с СДВГ и вариантами генетической сети глутамергической системы, нарушающими мGluR-сигнализацию
2017-12-27
SCID: 54.1/gsqzt4xj
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Clinical Global Impressions (CGI)adolescent ADHDfasoracetam (NFC-1)mGluR network variantsmetabotropic glutamate receptor
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Abstract (AI)
The glutamatergic neurotransmitter system may play an important role in attention-deficit hyperactivity disorder (ADHD). This 5-week, open-label, single-blind, placebo-controlled study reports the safety, pharmacokinetics and responsiveness of the metabotropic glutamate receptor (mGluR) activator fasoracetam (NFC-1), in 30 adolescents, age 12-17 years with ADHD, harboring mutations in mGluR network genes. Mutation status was double-blinded. A single-dose pharmacokinetic profiling from 50-800 mg was followed by a single-blind placebo at week 1 and subsequent symptom-driven dose advancement up to 400 mg BID for 4 weeks. NFC-1 treatment resulted in significant improvement. Mean Clinical Global Impressions-Improvement (CGI-I) and Severity (CGI-S) scores were, respectively, 3.79 at baseline vs. 2.33 at week 5 (P < 0.001) and 4.83 at baseline vs. 3.86 at week 5 (P < 0.001). Parental Vanderbilt scores showed significant improvement for subjects with mGluR Tier 1 variants (P < 0.035). There were no differences in the incidence of adverse events between placebo week and weeks on active drug. The trial is registered at https://clinicaltrials.gov/ct2/show/study/NCT02286817 .
Key Findings
1
Fasoracetam treatment produced significant clinical improvement: mean CGI-I improved from 3.79 at baseline to 2.33 at week 5 (P < 0.001).
2
Fasoracetam treatment produced significant reduction in severity: mean CGI-S improved from 4.83 at baseline to 3.86 at week 5 (P < 0.001).
3
In a 5-week open-label single-blind placebo-controlled study, fasoracetam (NFC-1) was administered to 30 adolescents (12–17) with ADHD and mGluR network gene mutations.
4
Parental Vanderbilt scores showed significant improvement specifically in subjects with mGluR Tier 1 variants (P < 0.035).
5
Single-dose pharmacokinetic profiling was performed across 50–800 mg, followed by symptom-driven dosing up to 400 mg twice daily for 4 weeks.
6
There were no differences in adverse event incidence between the single-blind placebo week and weeks on active fasoracetam, indicating comparable short-term tolerability.
Research Object
Adolescents (age 12–17) with ADHD harboring mutations in mGluR glutamatergic gene network
Research Subject
Safety, pharmacokinetics, and clinical responsiveness to the mGluR activator fasoracetam (NFC-1), including symptom improvement and adverse event incidence
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2017-12-27
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