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FDA Clears Cingulate to File NDA for CTx-1301 in the Treatment of ADHD

The company has announced plans to submit the NDA in the first half of 2025.

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American
Ann-childress
Shanej-schaffer
American-professional-society
Drug-administration
Behavior-medicine-inc
Cingulate-inc
New-drug-application
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Annual-meeting
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'It's not easy': Doctors are still figuring out adult ADHD

'It's not easy': Doctors are still figuring out adult ADHD
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FDA Clears Cingulate to File for Marketing Approval of

Phase 3 Data Collected to Date Sufficient for Submission of New Drug Application Advancing Discussions with Commercialization Partners.

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Kansas
Kansas-city
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FDA Clears Cingulate to File for Marketing Approval of CTx-1301 in the Treatment of ADHD

Phase 3 Data Collected to Date Sufficient for Submission of New Drug Application        CTx-1301 Could Benefit >60% of ADHD Patients Currently .

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Kansas-city
Kansas
American
Shanej-schaffer
Matt-kreps
Thomas-dalton
Ann-childress
Drug-administration
Behavior-medicine-inc
Platform-technology
Securities-exchange

Doctors Are Still Figuring Out Adult ADHD

Doctors Are Still Figuring Out Adult ADHD
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