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NCT02037074 · ClinicalTrials.gov registry record · Phase 1

Study to Assess the Safety, Tolerability, Pharmacokinetic (PK) and Pharmacodynamic (PD) Effects of EVP-6308 and the Potential of EVP-6308 to Affect the PK Properties of the Antipsychotic Regimen in Subjects With Schizophrenia Currently Receiving Stable Treatment With up to 2 Atypical Antipsychotics

A Phase 1 study, sponsored by FORUM Pharmaceuticals.

Completed
Registry status
Phase 1
Development phase
40
Enrollment target

NCT02037074 is a Phase 1 study that has completed, run by FORUM Pharmaceuticals. The registered enrollment target is 40 participants.

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The verdict

NCT02037074, a Phase 1 study, has completed, sponsored by FORUM Pharmaceuticals.

COMPLETED
Registry status
Phase 1
Development phase
40 participants
Enrollment target

Study Summary

This is a randomized, double-blind, placebo-controlled, sequential cohort, ascending oral dose study of the safety, tolerability, pharmacokinetics, and pharmacodynamics of EVP-6308 administered for 14 days in subjects with schizophrenia who are on a stable anti-psychotic regimen.

Interventions

  • DRUG Placebo
  • DRUG Drug: EVP-6308

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2014-06
Phase Phase 1

Sponsor

FORUM Pharmaceuticals

13 total trials

What the Registry Record Tells You About NCT02037074

The ClinicalTrials.gov registry entry for NCT02037074 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 40 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is FORUM Pharmaceuticals, which has 13 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT02037074 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT02037074 about?

NCT02037074 is a clinical study titled "Study to Assess the Safety, Tolerability, Pharmacokinetic (PK) and Pharmacodynamic (PD) Effects of EVP-6308 and the Potential of EVP-6308 to Affect the PK Properties of the Antipsychotic Regimen in Subjects With Schizophrenia Currently Receiving Stable Treatment With up to 2 Atypical Antipsychotics". This is a randomized, double-blind, placebo-controlled, sequential cohort, ascending oral dose study of the safety, tolerability, pharmacokinetics, and pharmacodynamics of EVP-6308 administered for 14 days in subjects with schizophrenia who are on a stable anti-psychotic regimen.

What is the current status of trial NCT02037074?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 40 participants. The study started on 2014-06.

What interventions are being tested in trial NCT02037074?

The interventions under investigation include: Placebo (DRUG), Drug: EVP-6308 (DRUG).

Who is sponsoring clinical trial NCT02037074?

This trial is sponsored by FORUM Pharmaceuticals, which has 13 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.