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Bioequivalence Study of Lisinopril and Hydrochlorothiazide Tablets (20+25) mg Under Fasting Conditions

NCT01831700 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 48

Last updated 2013-04-15

No results posted yet for this study

Summary

This is a randomized, open Label, balanced, two-treatment, two-period, two-sequence, single dose, cross over pivotal study. The purpose of this study is to assess the bioequivalence between Test Product and the corresponding Reference Product under fasting condition in normal, healthy, adult, human subjects.

Conditions

  • Fasting

Interventions

DRUG

Lisinopril and Hydrochlorothiazide Tablets (20+25) mg

Lisinopril and Hydrochlorothiazide (20+25) mg Tablets once a day

DRUG

Zestoretic® 20/25 lisinopril/hydrochlorothiazide Tablets

Zestoretic® 20/25 lisinopril/hydrochlorothiazide Tablets once a day

Sponsors & Collaborators

  • IPCA Laboratories Ltd.

    lead INDUSTRY

Principal Investigators

  • Dr. Tarang Girishbhai Shah, M. D. (Pharmacology) · Accutest Research Lab (I) Pvt. Ltd.

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2012-10-31
Primary Completion
2012-10-31
Completion
2012-10-31

Countries

  • India

Study Locations

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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 NCT01831700 on ClinicalTrials.gov