Bioequivalence Study of Fluoxetine HCL 40 mg Capsules Under Fasting Conditions

NCT00778024 | Completed DMC

• 1 other identifier: 03197
• Study Type: interventional
• Target: 36
• Locations: 1 country
• Sites: 1

Brief Summary

The objective of this study is to compare the relative bioavailability of fluoxetine HCL 40 mg capsules (by Ranbaxy Laboratories Limited) with that of PROZAC® 40 mg capsules (by Dista Products Company) following a single oral dose (1 x 40 mg capsule) in healthy, adult subjects under fasting conditions

Conditions

Healthy

Keywords

Bioequivalence fluoxetine HCL 40 mg capsules fasting conditions

Outcome Measures

Primary Outcomes (1)

• Bioequivalence

Study Arms (2)

1

EXPERIMENTAL

fluoxetine HCL 40 mg capsules of ranbaxy

Drug: fluoxetine HCL 40 mg capsules

2

ACTIVE COMPARATOR

PROZAC® 40 mg capsules

Drug: fluoxetine HCL 40 mg capsules

Interventions

fluoxetine HCL 40 mg capsules DRUG

1; 2

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Sex: Male and Female; similar proportion of each preferred.
• Age: At least 18 years.
• Qualifying subjects must be in good health and physical condition as determined by medical history, complete physical examination, and laboratory tests, all obtained within four (4) weeks prior to study start. The subject may not have a history of significant past illness expected to affect the investigation. The normal status of subjects will be confirmed by the following procedures:
• Laboratory Tests: Hemoglobin, hematocrit, RBC, WBC, differential count, serum electrolytes (Na, K, CL), fasting blood glucose, BUN, bilirubin, creatinine, AST, ALT, LD, alkaline phosphatase, and urinalysis. HIV, Hepatitis B, Hepatitis C, and drugs of abuse testing will be done for screening purposes only. Urine drugs of abuse testing will be repeated at each check-in. Female subjects will have a serum pregnancy test done at screening and urine pregnancy test prior to each study period at check-in. Laboratory values which are greater than :E20% of the normal range will not qualify unless specifically accepted (with comment) by the Principal Investigator. Results of HIV, Hepatitis B, Hepatitis C, and drugs of abuse must be negative or non-reactive for the subject to qualify for the study.
• Electrocardiogram: A 12-lead electrocardiogram (ECG) will be obtained for all subjects. The original tracings, plus interpretation, will be included in the case report form packet.
• Subjects must read and sign the Consent Form.

You may not qualify if:

• In addition, any one of the conditions listed below will exclude a subject from the study:
• History of treatment for alcoholism, substance abuse, or drug abuse within past 24 months.
• History of malignancy, stroke, diabetes, cardiac, renal or liver disease, or other serious illness.
• History of GERD (gastroesophageal reflux disease), malabsorption syndrome, colon cancer, or chronic colitis, including Crohn's disease.
• History of treatment for astlzurta within the past five (5) years.
• History of neurological impairment.
• History of seizures.
• History of Parkinson's Disease.
• History of diabetes mellitus.
• Females who are pregnant or lactating.
• History of hypersensitivity to fluoxetine HCL, or any serotonin reuptake inhibitor.
• Conditions upon screening which might contraindicate or require that caution be used in the administration of fluoxetlne HCL, including:
• Sitting systolic blood pressure below 90 mm Hg, or diastolic Pressure below 50 mm Hg.
• Heart rate less than 50 beats per minute after a 5-minute rest
• Inability to read and/or sign the consent form.

Sponsors & Collaborators

• Ranbaxy Laboratories Limited: lead

Study Sites (1)

Gateway medical research

Saint Charles, Missouri, 63301, United States

Location

Related Links

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MeSH Terms

Interventions

Fluoxetine

Intervention Hierarchy (Ancestors)

Propylamines; Amines; Organic Chemicals

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: NONE
• Intervention Model: CROSSOVER
• Sponsor Type: INDUSTRY

Study Record Dates

• First Submitted: October 22, 2008
• First Posted: October 23, 2008
• Study Start: August 1, 2003
• Primary Completion: October 1, 2003
• Study Completion: December 1, 2003
• Last Updated: December 15, 2009

Record last verified: 2009-12

Locations

US (1)