Ignite Creation Date:
2025-12-26 @ 10:34 AM
Ignite Modification Date:
2025-12-29 @ 8:04 AM
Study NCT ID:
NCT01131728
Status:
COMPLETED
Last Update Posted:
2010-06-14
First Post:
2010-05-26
Is Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
Bioequivalence Study of Naproxen Sodium 220 mg & Pseudoephedrine HCl 120 mg ER Tablets of Dr. Reddy's Under Fasting Conditions
Sponsor:
Organization:
Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'interventionBrowseModule': {'meshes': [{'id': 'D009288', 'term': 'Naproxen'}, {'id': 'D054199', 'term': 'Pseudoephedrine'}], 'ancestors': [{'id': 'D009280', 'term': 'Naphthaleneacetic Acids'}, {'id': 'D009281', 'term': 'Naphthalenes'}, {'id': 'D011084', 'term': 'Polycyclic Aromatic Hydrocarbons'}, {'id': 'D006841', 'term': 'Hydrocarbons, Aromatic'}, {'id': 'D006844', 'term': 'Hydrocarbons, Cyclic'}, {'id': 'D006838', 'term': 'Hydrocarbons'}, {'id': 'D009930', 'term': 'Organic Chemicals'}, {'id': 'D011083', 'term': 'Polycyclic Compounds'}, {'id': 'D011412', 'term': 'Propanolamines'}, {'id': 'D000605', 'term': 'Amino Alcohols'}, {'id': 'D000438', 'term': 'Alcohols'}, {'id': 'D020005', 'term': 'Propanols'}, {'id': 'D000588', 'term': 'Amines'}, {'id': 'D010627', 'term': 'Phenethylamines'}, {'id': 'D005021', 'term': 'Ethylamines'}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE1'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'RANDOMIZED', 'maskingInfo': {'masking': 'NONE'}, 'primaryPurpose': 'TREATMENT', 'interventionModel': 'CROSSOVER'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 26}}, 'statusModule': {'overallStatus': 'COMPLETED', 'startDateStruct': {'date': '2004-07'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2010-06', 'completionDateStruct': {'date': '2004-09', 'type': 'ACTUAL'}, 'lastUpdateSubmitDate': '2010-06-11', 'studyFirstSubmitDate': '2010-05-26', 'studyFirstSubmitQcDate': '2010-05-26', 'lastUpdatePostDateStruct': {'date': '2010-06-14', 'type': 'ESTIMATED'}, 'studyFirstPostDateStruct': {'date': '2010-05-27', 'type': 'ESTIMATED'}, 'primaryCompletionDateStruct': {'date': '2004-08', 'type': 'ACTUAL'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Bioequivalence based on Cmax and AUC parameters', 'timeFrame': '3 months'}]}, 'oversightModule': {'oversightHasDmc': False}, 'conditionsModule': {'keywords': ['Bioequivalence', 'Crossover', 'Naproxen Sodium and Pseudoephedrine Hydrochloride'], 'conditions': ['Healthy']}, 'descriptionModule': {'briefSummary': 'The purpose of this study is to assess the bioequivalence of Naproxen sodium 220 mg + Pseudoephedrine Hydrochloride 120 mg Extended Release tablets of with Aleve Cold and Sinus in healthy adult human subjects, under fasting conditions.', 'detailedDescription': 'Open randomized, two treatment, two period, two sequence, single dose, crossover study of 26 healthy human adult subjects under fasting conditions with a washout period of 14 days.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT'], 'maximumAge': '45 Years', 'minimumAge': '18 Years', 'healthyVolunteers': True, 'eligibilityCriteria': 'Inclusion Criteria:\n\nSubjects must fulfill all of the following criteria to be considered for inclusion into this study:\n\n* Subjects will provide written informed consent.\n* Subjects must be healthy human beings within 18-45 years of age (inclusive) weighing at least 50 kg.\n* Subjects must be within ±15% of ideal body weight in relation to height according to Life Insurance Corporation of India height-weight chart for non- medical cases.\n* Subjects must be of normal health as determined by medical history and physical examination performed within 21 days prior to the commencement of the study.\n* Have normal ECG, X-ray and vital signs.\n* Availability of subject for the entire study period and willingness to adhere to protocol requirements as evidenced by written informed consent.\n\nIf subject is a female volunteer and\n\n* Is 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.\n* Is postmenopausal for at least 1 year.\n* Is surgically sterile (bilateral tubal ligation, bilateral oophorectomy, or hysterectomy has been performed on the subject.\n\nExclusion Criteria:\n\nThe subjects will be excluded under following conditions:\n\nHistory or presence of significant:\n\n* Cardiovascular, pulmonary, hepatic, renal, hematological, gastrointestinal, endocrine,immunologic, dermatologic, musculoskeletal, neurological or psychiatric disease.\n* Alcohol dependence, alcohol abuse or drug abuse within past one year.\n* Moderate to heavy smoking (\\>10 cigarettes/day) or consumption of tobacco products.\n* Asthma, urticaria or other allergic type reactions after taking any medication.\n\nSubjects who through completion of the study, would have donated in excess of\n\n* 500 ml of blood in 14 days, or\n* 500 - 800ml of blood in 14 days (unless approved by the Principal Investigator)\n* 1000 ml of blood in 90 days\n* 1250 ml of blood in 120 days\n* 1500 ml of blood in 180 days\n* 2000 ml of blood in 270 days\n* 2500 ml of blood in 1 year Subjects who have participated in another clinical trial within 3 months of study start.\n\nSubjects who have:\n\n* Systolic blood pressure less than 90 mm of Hg and higher than 150 mm of Hg\n* Diastolic blood pressure less than 60 mm of Hg and more than 95 mm of Hg. Minor deviations (1-3 mm Hg) at check-in may be acceptable at the discretion of the physician/investigator.\n* Pulse rate below 50/min. and above 105/min. Female volunteers demonstrating a positive pregnancy screen or currently breast-feeding.'}, 'identificationModule': {'nctId': 'NCT01131728', 'briefTitle': "Bioequivalence Study of Naproxen Sodium 220 mg & Pseudoephedrine HCl 120 mg ER Tablets of Dr. Reddy's Under Fasting Conditions", 'organization': {'class': 'INDUSTRY', 'fullName': "Dr. Reddy's Laboratories Limited"}, 'officialTitle': 'A Randomized, Open Label, Two Treatment, Two Period, Two Sequence, Single Dose, Crossover, Bioequivalence Study of Naproxen Sodium 220 mg + Pseudoephedrine HCL 120 mg ER Tablets and Aleve Cold and Sinus® Under Fasting Conditions.', 'orgStudyIdInfo': {'id': '391/04'}}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'Naproxen Sodium & Pseudoephedrine HCl', 'description': "Naproxen Sodium 220 mg and Pseudoephedrine Hydrochloride 120 mg ER Tablets of Dr. Reddy's Laboratories.", 'interventionNames': ['Drug: Naproxen Sodium & Pseudoephedrine HCl']}, {'type': 'ACTIVE_COMPARATOR', 'label': 'Aleve Cold and Sinus', 'description': 'Aleve Cold and Sinus(Naproxen Sodium 220 mg and Pseudoephedrine Hydrochloride 120 mg Extended Release Tablets).', 'interventionNames': ['Drug: Naproxen Sodium & Pseudoephedrine HCl']}], 'interventions': [{'name': 'Naproxen Sodium & Pseudoephedrine HCl', 'type': 'DRUG', 'otherNames': ['Aleve Cold and Sinus'], 'description': 'Naproxen Sodium 220 mg and Pseudoephedrine Hydrochloride 120 mg Extended Release Tablets', 'armGroupLabels': ['Aleve Cold and Sinus', 'Naproxen Sodium & Pseudoephedrine HCl']}]}, 'contactsLocationsModule': {'locations': [{'zip': '560034', 'city': 'Bangalore', 'state': 'Karnataka', 'country': 'India', 'facility': 'Lotus Labs Private Limited', 'geoPoint': {'lat': 12.97194, 'lon': 77.59369}}], 'overallOfficials': [{'name': 'Sandhya Ravi, MBBS, MS.', 'role': 'PRINCIPAL_INVESTIGATOR', 'affiliation': 'Lotus Labs Pvt. Ltd.,'}]}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': "Dr. Reddy's Laboratories Limited", 'class': 'INDUSTRY'}, 'responsibleParty': {'oldNameTitle': 'M.S. Mohan / Vice President, R&D', 'oldOrganization': "Dr. Reddy's Laboratories Limited"}}}}