Steady State Bioequivalence Study of Torrent Pharmaceuticals Ltd's Bioequivalence Study of Torrent Pharmaceuticals Ltd's Quetiapine Tablets

Phase 1

Completed

• Conditions: Schizophrenia

• Registration Number: NCT01634373
• Lead Sponsor: Torrent Pharmaceuticals Limited

Brief Summary

Objective:

Primary objective was to study Steady-state bioequivalence of Torrent's Quetiapine Fumarate Tablets 300 mg.

Study Design:

Randomized, Two-Way, Crossover, multiple Dose, and Open-Label

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2012-06-27
• Status Verified: 2012-07
• Study First Submitted QC: 2012-07-02
• Last Update Submitted: 2012-07-02
• Study First Posted: 2012-07-06
• Last Update Posted: 2012-07-06

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

• Sex: Male of female
• Age: 25-65 years
• Patients who are receiving a stable daily dose of quetiapine 300 mg every 12 hourly for atlist one month
• Patient willing to adhere to the protocol requirements

Exclusion Criteria

• Clinically relevant abnormalities in the results of the laboratory screening evaluation.
• Clinically significant abnormal ECG.
• Significant orthostatic hypotension (i.e., a drop in systolic blood pressure of 30 mm Hg or more and/or a drop in diastolic blood pressure of 20 mm Hg or more on standing)
• Concurrent use of antihypertensive medication or any medication that might pre-dispose to orthostatic hypotension.
• History of allergic reactions to quetiapine or other chemically related psychotropic drugs.
• Concurrent primary psychiatric or neurological diagnosis including organic mental disorder, severe tardive dyskinesia, or idiopathic Parkinson's disease.
• Existence of any surgical or medical condition, which in the judgement of the Principal Investigator, might interfere with the absorption, distribution, metabolism or excretion of the drug or likely to compromise the safety of patients.
• Concurrent use of other drugs known to suppress bone marrow function.
• HIV, HCV, HBsAg positive.
• Expected changes in concomitant medications during the period of study.
• A history of epilepsy or risk for seizures
• positive urine drug of abuse test at enrollment.
• A history of alcohol or drug dependence by Diagnostic and statistical manual of Mental disorders IV(DSM-IV) criteria during the 6 month period immediately prior to study entry.
• A total white blood cell count below 4000/ml, or absolute neutrophil count below 2000/ml
• Female patients with pregnancy or Breast feeding or intend to become pregnant during the study and not able to follow contraception methods.
• History of multiple syncopal episodes.
• Administration any study drugs in last 3 months prior to entry in the study.
• History of significant blood loss due to any reason in the past 3 months.
• Any pre-existing bleeding disorder.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: Not specified

Trial Locations

Locations (1)

Asha Hospital; 🇮🇳 Hyderabad, India