Randomized Withdrawal Study in Patients With Schizophrenia

ConditionSchizophrenia
Trial statusRecruiting
Trial phasePhase 3
Trial typeInterventional
Biological sexAll
Age18-65
SponsorVanda Pharmaceuticals

About this trial

The purpose of this research is to evaluate the efficacy of dosing iloperidone long-acting injection (LAI) compared to placebo in preventing the exacerbation of symptoms in patients with schizophrenia.

Eligibility criteria

Qualifiers

Males or females 18 to 65 years of age (inclusive)

Diagnosed with schizophrenia per DSM-5 criteria

In need of ongoing psychiatric treatment

Disqualifiers

DSM-5 diagnosis of a psychiatric disorder other than schizophrenia that was the primary focus of treatment within the previous six months

Trial design

Treatments tested in this trial

  • iloperidone
  • placebo

Treatment groups

400 Participants
are divided into 2 treatment groups

Sponsors and collaborators