Flexible-dose, Long-term Safety Study of Lu AF35700 in Adult Patients With Schizophrenia

Safety study in patients with schizophrenia who have participated and completed a study
investigating Lu AF35700 including Studies 16159A and 16323A. Or in patients with
schizophrenia for whom a switch of antipsychotic treatment can be potentially beneficial
according to the investigator's clinical judgement.

Inclusion Criteria:

- For 16159A-patients

- The patient has completed Study 16159A.

- The patient is able to read and understand the Informed Consent Form.

- The patient has signed the Informed Consent Form specific for Study 16159B.

- The patient can potentially benefit from 52-week treatment with Lu AF35700 according
to the investigator's clinical judgement.

For 16323A-patients

- The patient has completed the dosing period of Study 16323A.

- The patient is able to read and understand the Informed Consent Form.

- The patient has signed the Informed Consent Form specific Study 16159B.

- The patient has a confirmed diagnosis of schizophrenia according to DSM-5™.

- The patient can potentially benefit from 52-week treatment with Lu AF35700 according
to the investigator's clinical judgement.

For Other Patients

- The patient has schizophrenia, diagnosed according to DSM-5™.

- The patient is a man or woman, aged ≥18 years.

- The patient has been prescribed oral antipsychotic treatment at the recommended dose
range as stated in the summary of product characteristics or equivalent label for 6
weeks prior to the Screening Visit.

- The patient has a PANSS total score ≥60 and ≤90 at Screening and Baseline Visits.

- The patient has a Clinical Global Impression - Severity of Illness (CGI-S) score ≤4.

- The patient is in need of a change in the current antipsychotic treatment and,
according to the investigator's clinical judgement, the patient can potentially
benefit from a switch to another treatment including, but not limited to, any of the
following reasons:

- lack of adequate response to his or her current antipsychotic medication;

- poor tolerability to his or her current antipsychotic medication;

- unwillingness of the patient to adhere to his or her current antipsychotic
medication.

Exclusion Criteria:

- For 16159A-patients

- The patient has been diagnosed with a primary psychiatric disorder other than
schizophrenia during Study 16159A.

- The patient, in the opinion of the investigator, is at significant risk of suicide,
or: Answers "Yes" to any question on the Suicidal Behaviour section of the
Columbia-Suicide Severity Rating Scale (C-SSRS), OR Answers "Yes" to questions 4 and 5
on the Suicidal Ideation section of the C-SSRS

For 16323A-patients

- The patient has been diagnosed with a primary psychiatric disorder other than
schizophrenia during Study 16323A.

- The patient, in the opinion of the investigator, is at significant risk of suicide,
or: Answers "Yes" to any question on the Suicidal Behaviour section of the C-SSRS, OR
Answers "Yes" to questions 4 and 5 on the Suicidal Ideation section of the C-SSRS

For Other Patients

- The patient has any current psychiatric disorder (DSM-5™ criteria) other than
schizophrenia established as the primary diagnosis.

- The patient is experiencing acute exacerbation of psychotic symptoms at the Screening
Visit, between the Screening and Baseline Visits or at the Baseline Visit.

- The patient is treated with clozapine at the time of the Screening Visit.

- The patient has a substance use disorder (except nicotine) which according to the
investigator's judgment may compromise the patient's ability to comply with the study
procedures, or preclude the benefits of the study medication.

- The patient, in the opinion of the investigator, is at significant risk of suicide,
or: Answers "Yes" to any question on the Suicidal Behaviour section of the C-SSRS, OR
Answers "Yes" to questions 4 and 5 on the Suicidal Ideation section of the C-SSRS

Other protocol defined inclusion and exclusion criteria may apply