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Otsuka Pharmaceutical Reports Results from Two P-III Trials of Centanafadine to Treat ADHD

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Otsuka Pharmaceutical Reports Results from Two P-III Trials of Centanafadine to Treat ADHD

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  • Both P-III clinical trials (NCT05257265) & (NCT05428033) evaluated the safety, efficacy & tolerability of Centanafadine (high/low dose) vs PBO in adolescents (aged 13-17yrs. & 6-12yrs.) with attention-deficit/hyperactivity disorder (ADHD) across the US & Canada
  • The results from both trials depicted a change from baseline at 6wks. on the ADHD-RS-5 scale along with a statically significant improvement in high dose cohort vs PBO whereas the low-dose cohorts did not reach statistical significance
  • Centanafadine, a norepinephrine, dopamine, and serotonin reuptake inhibitor, is currently under clinical studies following which the company plans to submit an NDA to the US FDA

Ref: Businesswire | Image: Otsuka

Related News:- Otsuka and Astex Receive EC’s Approval for Inaqovi (decitabine and cedazuridine) to Treat Newly Diagnosed Acute Myeloid Leukaemia

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Shivani Chandra

Shivani was a content writer at PharmaShots. She has a keen interest in recent innovations in the life sciences industry. She was covering news related to Product approvals, clinical trial results, and updates. We can be contacted at connect@pharmashots.com.

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