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NCT01952132 · ClinicalTrials.gov registry record · Phase 2

Safety, Tolerability, and Pharmacokinetics of OMS643762 in Psychiatrically Stable Schizophrenia Subjects

A Phase 2 study of Schizophrenia, sponsored by Omeros Corporation.

Completed
Registry status
Phase 2
Development phase
40
Enrollment target
1
Study location

NCT01952132: Completed Phase 2 study of Schizophrenia, sponsored by Omeros Corporation.

NCT01952132 is a Phase 2 study of Schizophrenia that has completed, run by Omeros Corporation. The registered enrollment target is 40 participants, below the 219-participant average among 315 other Schizophrenia trials with a reported enrollment target (82% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01952132, a Phase 2 study of Schizophrenia, has completed, sponsored by Omeros Corporation.

COMPLETED
Registry status
Phase 2
Development phase
40 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to determine the safety, tolerability and pharmacokinetics of OMS643762 (the study drug) in psychiatrically stable schizophrenia patients.

Primary Outcome

Incidence of adverse events

Conditions Studied

Interventions

  • DRUG Placebo
  • DRUG OMS643762

Study Locations (1)

California

  • - Long Beach

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2013-09
Est. Completion 2014-04
Phase Phase 2
Omeros Corporation

19 total trials

What the finished NCT01952132 record still lists

NCT01952132 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 219-participant average among 315 other Schizophrenia trials with a reported enrollment target (82% lower).

The record links to 1 condition, with Schizophrenia appearing as the primary indexed condition, and to 2 interventions - of which Placebo is the first listed.

NCT01952132 reports a single indexed study location in California.

Frequently Asked Questions

What is clinical trial NCT01952132 about?

NCT01952132 is a clinical study titled "Safety, Tolerability, and Pharmacokinetics of OMS643762 in Psychiatrically Stable Schizophrenia Subjects". The purpose of this study is to determine the safety, tolerability and pharmacokinetics of OMS643762 (the study drug) in psychiatrically stable schizophrenia patients.

What is the current status of trial NCT01952132?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 40 participants. The study started on 2013-09. Estimated completion is 2014-04.

What conditions does trial NCT01952132 study?

This clinical trial studies the following conditions: Schizophrenia.

What interventions are being tested in trial NCT01952132?

The interventions under investigation include: Placebo (DRUG), OMS643762 (DRUG).

Who is sponsoring clinical trial NCT01952132?

This trial is sponsored by Omeros Corporation, which has 19 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01952132 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Schizophrenia

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT01952132's enrollment target sits among peer trials

40 233rd of 315 higher than 73 of 315 other Schizophrenia trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Schizophrenia trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01952132, the US trial registry maintained by the National Library of Medicine. NCT01952132 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.