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CompletedNCT07191483

A Study to Evaluate KYN-5356 in Adults With Cognitive Impairment Associated With Schizophrenia

Medication studyAges 18–55United States
The study in practice

Understand this study

Who was this study for?

This study was for people with schizophrenia. Listed age limits: 18 years to 55 years. Other eligibility criteria applied.

Listed locations
Little Rock and 14 more locationsSee all locations and recruitment
Study phase
Phase 2Usually explores whether the intervention may work, while continuing to monitor safety.

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Study clarity

Study information

Study start dateStarted: August 27, 2025
Recruitment status
Completed
Enrollment listed in the registry
149
Sponsor
Kynexis B.V.
Sponsor type
Unknown or unclear
Study type
Drug
Intervention type
Medication / drug, OTHER
Study phase
Phase 2Usually explores whether the intervention may work, while continuing to monitor safety.
Locations
United States
Age range
From 18 Years to 55 Years
Official registry ID
NCT07191483
Official title
Show the full official title

A Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy, Safety, Pharmacokinetics (PK), and Pharmacodynamics (PD) of KYN-5356 as Adjunctive Treatment in Adults With Cognitive Impairment Associated With Schizophrenia

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Recruitment & locations

Completed

Little Rock · Cerritos · Lemon Grove

12 more locations
  • Los Alamitos
  • Boynton Beach
  • Hollywood
  • Miami Lakes
  • Atlanta
  • Decatur
  • Chicago
  • Gaithersburg
  • St Louis
  • Marlton
  • North Canton
  • Austin
FAQ

Questions about this study

Who is behind this study?

The study sponsor is Kynexis B.V.

Did this study involve medication?

Yes. The study involved medication, including KYN-5356 low dose, KYN-5356 Medium Dose and KYN-5356 High Dose.

Who was this study for?

This study was for people with schizophrenia. Listed age limits: 18 years to 55 years. Other eligibility criteria applied.

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