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
Håkon Håkonarson, Enda M. Byrne, Brian D. Sykes, Leslie A. Lange, Charlly Kao, Rosetta Chiavacci, Ganesh S. Moorthy, Josephine Elia, Joshua Davis, Athena F. Zuppa, Grace Ungal, Alexander Ambrosini, Nilsa De Jesus-Rosario, Lene Larsen, Tiancheng Wang, Christine Kurian, Kanani Titchen, Sharon Hwang, Bhumi Kumar, Jacqueline Potts, Jeffrey Malatack, Emma Slattery, Andrew E. Weller, Walter K. Kraft
2017-12-27

Clinical Global Impressions (CGI)adolescent ADHDfasoracetam (NFC-1)mGluR network variantsmetabotropic glutamate receptor
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 .
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.

Adolescents (age 12–17) with ADHD harboring mutations in mGluR glutamatergic gene network

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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Authors
Håkon Håkonarson
Enda M. Byrne
Brian D. Sykes
Leslie A. Lange
Charlly Kao
Rosetta Chiavacci
Ganesh S. Moorthy
Josephine Elia
Joshua Davis
Athena F. Zuppa
Grace Ungal
Alexander Ambrosini
Nilsa De Jesus-Rosario
Lene Larsen
Tiancheng Wang
Christine Kurian
Kanani Titchen
Sharon Hwang
Bhumi Kumar
Jacqueline Potts
Jeffrey Malatack
Emma Slattery
Andrew E. Weller
Walter K. Kraft
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