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Bioequivalence Study of Lansoprazole DR Capsules 30 mg in Fasting Conditions

This study has been completed.
Information provided by:
Dr. Reddy's Laboratories Limited Identifier:
First received: January 3, 2011
Last updated: January 4, 2011
Last verified: February 2009
The objective of this study was to compare the relative bioavailability of Lansoprazole DR Capsules 30 mg with Prevacid® Capsules 30 mg under fasting conditions in healthy adult human subjects.

Condition Intervention Phase
Drug: Lansoprazole
Phase 1

Study Type: Interventional
Study Design: Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: Open Label
Primary Purpose: Treatment
Official Title: Open Label, Randomized, Two-treatment, Three-period, Three-sequence, Partial Replicate Oral Bioequivalence Study of Lansoprazole 30 mg DR Capsules of Dr.Reddy's Laboratories Limited, India Comparing With That of PREVACID® (Containing Lansoprazole) 30 mg DR Capsules of TAP Pharmaceuticals Inc. USA, in Healthy, Adult, Human Subjects Under Fasting Conditions.

Resource links provided by NLM:

Further study details as provided by Dr. Reddy's Laboratories Limited:

Primary Outcome Measures:
  • Bioequivalence based on Cmax and AUC parameters [ Time Frame: 4 months ]

Enrollment: 48
Study Start Date: December 2008
Study Completion Date: December 2008
Primary Completion Date: December 2008 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Lansoprazole DR Capsules 30 mg
Lansoprazole DR Capsules 30 mg of Dr.Reddy's Laboratories Limited
Drug: Lansoprazole
Lansoprazole DR Capsules 30 mg
Other Name: Prevacid
Active Comparator: Prevacid 30 mg Capsules
Prevacid 30 mg Capsules of TAP Pharmaceuticals Inc. USA
Drug: Lansoprazole
Lansoprazole DR Capsules 30 mg
Other Name: Prevacid

Detailed Description:
open label, randomized, two-treatment, three-period, three-sequence, partial replicate oral bioequivalence study of Lansoprazole 30 mg DR Capsules of Dr.Reddy's Laboratories Limited, India comparing with that of PREVACID® (containing Lansoprazole) 30 mg DR Capsules of TAP Pharmaceuticals Inc. USA, in healthy, adult, human subjects under fasting conditions. 48 healthy, adult, human subjects were enrolled in the study and 42 subjects were completed the study.

Ages Eligible for Study:   18 Years to 45 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes

Inclusion Criteria:

i. Provided written informed consent.

ii. Subject who were healthy, adult, human beings within 18 and 45 years of age (both inclusive) weighing at least 50 kg.

iii. Subject having a body mass index between 18.0 and 29.9 (both inclusive), calculated as weight in Kg/height in m2.

iv. Subject having a normal health as determined by medical history, physical examination and laboratory investigation performed within 28 days prior to the commencement of the study. (Laboratory values must be within normal limits or considered by the physician /investigator to be of no clinical significance).

v. Female Subjects of child bearing potential practicing an acceptable method of birth control for the duration of the study as judged by the investigator(s), such as condoms, foams, jellies, diaphragm, intrauterine device (IUD), or abstinence.

  • postmenopausal for at least 1 year.
  • surgically sterile (bilateral tubal ligation, bilateral oophorectomy, or hysterectomy has been performed on the subject)

Exclusion Criteria:

i. Subject who were incapable of understanding the informed consent.

ii. Systolic blood pressure less than 90 mm of Hg or more than 140 mm of Hg.

iii. Diastolic blood pressure less than 60 mm of Hg or more than 90 mm of Hg.

iv. Oral temperature is below 95.0°F or above 98.6°F.

v. Pulse rate below 50/min or above 100/min.

vi. History of hypersensitivity or idiosyncratic reaction to investigational drug product or any other related drugs.

vii. Any evidence of impairment of renal, hepatic, cardiac, lung or gastrointestinal function.

viii. Consumption of grapefruit for the past ten days prior to the check-in, in each period.

ix. Regular smoker who has a habit of smoking more than nine cigarettes per day and has difficulty in abstaining from smoking during sample collection period.

x. Habit of alcoholism and difficulty in abstaining from alcohol during the sample collection period.

xi. Difficulty in abstaining from xanthene containing food or beverages (like tea, coffee, chocolates and cola drinks) during the sample collection period.

xii. Intake of over the counter (OTC) or prescribed medications and enzyme modifying medication or systemic medication for the last 30 days before dosing.

xiii. Clinically significant abnormalities and / or with significant diseases.

xiv. Confirmed positive in alcohol screening.

xv. Confirmed positive in selected drug of abuse.

xvi. Subjects who had participated in any other clinical investigation using experimental drug/donated blood in past 90 days before the date of start of study

xvii. Confirmed positive in urine pregnancy test.

xviii. Female detected to be pregnant, breast feeding or who is likely to become pregnant during the study.

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Please refer to this study by its identifier: NCT01270308

Bioserve Clinical Research (P) Ltd
Balanagar, Hyderabad, India, 500 037
Sponsors and Collaborators
Dr. Reddy's Laboratories Limited
Principal Investigator: Dr.M.Venkat Jayanth, MBBS Bioserve Clinical Research (P) Ltd
  More Information

Responsible Party: Manager - Research & Development, Dr. Reddy's Laboratories Limited Identifier: NCT01270308     History of Changes
Other Study ID Numbers: P-699/08
Study First Received: January 3, 2011
Last Updated: January 4, 2011

Keywords provided by Dr. Reddy's Laboratories Limited:
two way crossover

Additional relevant MeSH terms:
Anti-Ulcer Agents
Gastrointestinal Agents
Proton Pump Inhibitors
Enzyme Inhibitors
Molecular Mechanisms of Pharmacological Action processed this record on April 28, 2017