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pdufa.bio

Centanafadine

Updated ·next FDA decision on the calendar

Centanafadine is a Otsuka Pharmaceutical program in ADHD in adults and pediatric patients aged 6 years and older (≥20kg). The FDA approved it on Jul 24, 2026. 1 FDA decision on record below. Every date links its source.

OTSKY catalyst hub

All upcoming FDA decision dates on the 2026 PDUFA calendar

About this program

Indication under review: ADHD in adults and pediatric patients aged 6 years and older (≥20kg). Sponsor: Otsuka Pharmaceutical (OTSKY). Market-cap tier at the time we tracked it: Large. We track 1 catalyst event for this program: 0 upcoming and 1 in the record. A PDUFA date is the FDA's target date to complete review of a marketing application; a readout is the sponsor's expected date for clinical trial results. What a PDUFA date is · why we do not compare trial results across drugs.

Catalyst history

PDUFA · Jul 24, 2026 ✓ ApprovedOTSKY

Questions

When is Centanafadine's next FDA decision or readout?

No upcoming catalyst is on our calendar for Centanafadine; 1 FDA decision is on record below.

What happened at Centanafadine's most recent FDA decision?

On Jul 24, 2026 the FDA approved the application. The decision page carries the source document and the measured share-price reaction.

What is Centanafadine used for?

In our records Centanafadine is under review or in development for ADHD in adults and pediatric patients aged 6 years and older (≥20kg).

Who makes Centanafadine?

Otsuka Pharmaceutical (OTSKY).

Has Centanafadine been approved by the FDA?

Yes. The FDA approved an application for Centanafadine on Jul 24, 2026; the decision page linked above carries the source.

Where does this data come from?

FDA announcements, sponsor press releases and SEC filings; every date on this page links its source.