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Trial record 71 of 1447 for:    Area Under Curve AND tablet

Bioequivalence Study of Ropinirole Hydrochloride ER Tablets 2 mg Under Fasting Condition

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT01627834
Recruitment Status : Completed
First Posted : June 26, 2012
Last Update Posted : September 28, 2012
Information provided by (Responsible Party):
Dr. Reddy's Laboratories Limited

Brief Summary:
This is an open label, randomised, balanced, two-treatment, two-period, two-sequence, crossover, oral bioequivalence study.

Condition or disease Intervention/treatment Phase
Healthy Drug: Ropinirole Phase 1

Detailed Description:
The objective of this study was to determine the single-dose oral bioequivalence of Ropinirole Hydrochloride Extended Release Tablets 2 mg of Dr. Reddy's Laboratories Limited, India with REQUIP® XL (Ropinirole) 2 mg ER Tablets of Glaxosmithkline, USA, in normal, healthy, adult, human subjects under fasting condition.

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 48 participants
Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: Open Label, Balanced, Randomized, Two-treatment, Two-sequence, Two-period, Single-dose, Crossover Oral Bioequivalence Study of Ropinirole Hydrochloride Extended Release Tablets 2 mg of Dr. Reddy's Laboratories Limited, India With REQUIP@ XL (Ropinirole) 2 mg ER Tablets of Glaxosmithkline, USA, in Normal, Healthy, Adult, Human Subjects Under Fasting Condition.
Study Start Date : October 2009
Actual Primary Completion Date : October 2009
Actual Study Completion Date : November 2009

Resource links provided by the National Library of Medicine

Arm Intervention/treatment
Experimental: Ropinirole
Ropinirole Hydrochloride ER tablets 2 mg of Dr. Reddy's Laboratories Limited
Drug: Ropinirole
Other Name: Requip

Active Comparator: Requip
Requip XL Tablets 2 mg of Glaxosmithkline, USA
Drug: Ropinirole
Other Name: Requip

Primary Outcome Measures :
  1. Area under curve(AUC) [ Time Frame: Pre-dose (before dosing, in the morning of the day of dosing) and at 1.00, 2.00, 3.00,4.00, 5.00, 6.00, 7.00, 8.00, 9.00, 10.00, 11.00, 12.00, 13.00, 14.00, 15.00, 16.00, 17.00, 18.00,20.00, 24.00, 30.00, 36.00, 48.00 and 60.00 hours after dosing. ]

Information from the National Library of Medicine

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

Inclusion Criteria:

  1. Healthy human subjects aged between 18 and 45 years (including both).
  2. Subjects with a BMI between 18.5 - 24.9 Kg/m2 (including both) but body weight not less than 45 Kgs.
  3. Subjects with normal health as determined by personal medical history, clinical examination, and laboratory examinations including serological tests.
  4. Subjects having normal 12-lead electrocardiogram (ECG).
  5. Subjects having normal chest X-Ray (PIA view).
  6. Subjects able to communicate effectively.
  7. Subjects willing to give written informed consent and adhere to all the requirements of this protocol.
  8. Female subjects who are postmenopausal or surgically sterile.
  9. Female subjects 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.

Exclusion Criteria:

  1. Subjects having contraindications or hypersensitivity to ropinirole or domperidone or related group of drugs.
  2. History or presence of any medical condition or disease according to the opinion of the physician.
  3. History or presence of significant cardiovascular, pulmonary, hepatic, renal, gastrointestinal, endocrine, immunological, dermatological, neurological or psychiatric disease or disorder.
  4. History or presence of significant alcoholism or drug abuse in the past one year.
  5. History or presence of significant smoking (more than 10 cigarettes or bidis/day or consumption of tobacco products).
  6. Difficulty with donating blood.
  7. Difficulty in swallowing solids like tablets or capsules.
  8. Systolic blood pressure less than 110mm Hg or more than 140 mm Hg.
  9. Diastolic blood pressure less than 70 mm Hg or more than 90 mm Hg.
  10. Pulse rate less than 50 beats/minute or more than 100 beats/minute.
  11. Use of any prescribed medication during last two weeks or OTC medicinal products during the last one week preceding the first dosing.
  12. Major illness during 3 months before screening.
  13. Participation in a drug research study within past 3 months.
  14. Donation of blood in the past 3 months before screening.
  15. Female subjects demonstrating a positive pregnancy screen.
  16. Female subjects who are currently breast-feeding.
  17. Female subjects with child bearing potential using prohibited contraceptive method (Oral, Injectable or Implantable hormonal agents).

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT01627834

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GVK Biosciences Pvt. Ltd
Ameerpet, Hyderabad, India, 500 038
Sponsors and Collaborators
Dr. Reddy's Laboratories Limited
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Principal Investigator: Dr. Naba Kr Talukdar, MD GVK Biosciences Pvt. Ltd.

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Responsible Party: Dr. Reddy's Laboratories Limited Identifier: NCT01627834    
Other Study ID Numbers: 034-09
First Posted: June 26, 2012    Key Record Dates
Last Update Posted: September 28, 2012
Last Verified: January 2010
Keywords provided by Dr. Reddy's Laboratories Limited:
Ropinirole Hydrochloride
Additional relevant MeSH terms:
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Antiparkinson Agents
Anti-Dyskinesia Agents
Dopamine Agonists
Dopamine Agents
Neurotransmitter Agents
Molecular Mechanisms of Pharmacological Action
Physiological Effects of Drugs