deltatrials
Completed PHASE1 INTERVENTIONAL 1-arm NCT04712734

A Study to Evaluate Iloperidone Long-acting Injection (LAI) for the Treatment of Schizophrenia

An Open-label, Adaptive, Repeat-dose Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Iloperidone Long-acting Injection (LAI) in Patients With Schizophrenia

Sponsor: Vanda Pharmaceuticals

Conditions Schizophrenia
Interventions Iloperidone
Updated 6 times since 2021 Last updated: Jun 27, 2023 Started: Jan 13, 2021 Primary completion: Aug 30, 2022 Completion: Aug 30, 2022
This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

A PHASE1 clinical study on Schizophrenia, this trial is completed. The trial is conducted by Vanda Pharmaceuticals and has accumulated 6 data snapshots since 2021. Psychiatric clinical trials are essential for establishing evidence-based treatment standards.

Status Flow

~Feb 2021 – ~May 2021 · 3 months · monthly snapshotRecruiting~May 2021 – ~Jul 2022 · 14 months · monthly snapshotRecruiting~Jul 2022 – ~Jul 2023 · 12 months · monthly snapshotRecruiting~Jul 2023 – ~Jul 2024 · 12 months · monthly snapshotCompleted~Jul 2024 – ~Sep 2024 · 2 months · monthly snapshotCompleted~Sep 2024 – present · 20 months · monthly snapshotCompleted

Change History

6 versions recorded
  1. Sep 2024 — Present [monthly]

    Completed PHASE1

  2. Jul 2024 — Sep 2024 [monthly]

    Completed PHASE1

  3. Jul 2023 — Jul 2024 [monthly]

    Completed PHASE1

    Status: RecruitingCompleted

  4. Jul 2022 — Jul 2023 [monthly]

    Recruiting PHASE1

  5. May 2021 — Jul 2022 [monthly]

    Recruiting PHASE1

Show 1 earlier version
  1. Feb 2021 — May 2021 [monthly]

    Recruiting PHASE1

    First recorded

Jan 2021

Trial started

Per CT.gov start date — pre-dates our first snapshot

Eligibility Summary

No eligibility information available.

Contact Information

Sponsor contact:
  • Vanda Pharmaceuticals
Data source: Vanda Pharmaceuticals

For direct contact, visit the study record on ClinicalTrials.gov .