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Recruiting

Evaluation of Treatment Satisfaction and KarXT Utilization Registry (RESKU) - CN012-0066

Aggiornato: 20 luglio, 2026   |   ClinicalTrials.gov.

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Utilizzi la Guida per i partecipanti allo studio per esplorare il processo di partecipazione a una sperimentazione clinica. Comprenda i fattori chiave da considerare prima di decidere e pensi alle domande da porre al Suo team di professionisti sanitari.

Dettagli della sperimentazione

  • Sesso

  • 18+

    Fascia d'età

  • 17

    Sede/i

  • Recruiting

Opzioni di trattamento

Bracci dello studio
INTERVENTO ASSEGNATO
Participants receiving xanomeline and trospium chloride (XT) therapy
Drug: xanomeline and trospium chloride (XT) therapy

Principali criteri di idoneità

Inclusion Criteria: - Aged ≥18 years at index date. - Have a confirmed diagnosis of schizophrenia before index date. - Receipt of an initial prescription order for xanomeline and trospium chloride (XT) and plan to fill and initiate such therapy. - Provide a signed and dated Institutional Review Board (IRB)/Independent Ethics Committee (IEC)-approved written informed consent form (ICF) in accordance with regulatory, local, and institutional guidelines. - Agree to use an electronic device to record, or provide paper entry of, patient-reported outcomes (in English or Spanish). - English or Spanish speaking. Exclusion Criteria: - Participation in an interventional study within the last 30 days or plan to participate in such study at the time of eligibility screening. - Evidence of use of XT prior to time of eligibility screening.