Pharmacokinetic, Safety, and Tolerability Study of Risperidone ISM® at Different Dose Strengths

NCT01788774 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 36

Last updated 2023-10-23

No results posted yet for this study

Summary

This clinical trial is designed to evaluate different dosages of risperidone ISM, a new long-acting injectable form.

Conditions

Interventions

DRUG

Risperidone ISM 50 mg

DRUG

Risperidone ISM 75 mg

DRUG

Risperidone ISM 100 mg

Sponsors & Collaborators

  • Rovi Pharmaceuticals Laboratories

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-04-30
Primary Completion
2014-02-28
Completion
2014-02-28

Countries

  • Croatia
  • Russia
  • South Africa
  • Spain

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01788774 on ClinicalTrials.gov