Expired Study
This study is not currently recruiting Study Participants on ClinicalConnection.com. If you would like to find active studies please search for clinical trials.

Rockville, Maryland 20850


Purpose:

The purpose of this PET study is to verify the binding of Lu AF35700 after multiple oral dosing at the dopamine and the serotonin receptors in male patients with schizophrenia.


Criteria:

Inclusion Criteria: 1. The patient is a man aged between ≤18 and ≥60 years 2. BMI of ≥19 kg/m2 to ≤ 37 kg/m2 3. The patient has a primary diagnosis of schizophrenia according to DSM-5™ (code 295.90) 4. The patient has a Clinical Global Impression - Severity of Illness (CGI-S) score ≤ 4 (moderately ill) at screening and safety baseline 5. The patient is currently under oral therapy with one or more of the antipsychotic medications listed in Appendix II. 6. The patient has a Positive and Negative Syndrome Scale (PANSS) total score ≤ 80 7. The patient has a score of ≤ 4 (moderate) on the following PANSS items at screening and at safety baseline: P7 (hostility), G8 (uncooperativeness) Exclusion Criteria: 1. The patient experienced an acute exacerbation requiring hospitalization within the last 3 months. 2. The patient experienced an acute exacerbation requiring change in antipsychotic medication (with reference to drug or dose) within the last 4 weeks. 3. The patient has a diagnosis or history of substance use disorder (except nicotine) according to DSM-5-TR® criteria ≤3 months prior to screening 4. The patient is at significant risk of harming himself or others according to the investigator's judgment or as indicated by an answer of "yes" to the question 4 or 5 on the Columbia-Suicide Severity Rating Scale (C-SSRS) at the Screening Visit within the last six months on the lifetime version of C-SSRS. 5. Based on investigators judgment the patient has a medical or neurological disorder or treatment for such disorder that could interfere with the study treatment or impair treatment compliance. 6. The patient has had past episodes of extrapyramidal symptoms (EPS) under current medication within the last 6 month 7. The patient takes other medication than those listed as allowed concomitant medication in Appendix III 8. The patient is occupationally exposed to significant levels of ionizing radiation. Other protocol-defined inclusion and exclusion criteria may apply


NCT ID:

NCT02333487


Primary Contact:

Study Director
Email contact via H. Lundbeck
LundbeckClinicalTrials@lundbeck.com


Backup Contact:

N/A


Location Contact:

Rockville, Maryland 20850
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: January 21, 2020

Modifications to this listing: Only selected fields are shown, please use the link below to view all information about this clinical trial.


Click to view Full Listing

This study is not currently recruiting Study Participants on ClinicalConnection.com. The form below is not enabled.