A Relative Bioavailability Study of Griseofulvin 125 mg/5 mL Suspension Under Fasting Conditions

NCT ID: NCT00864071

Last Updated: 2010-08-16

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 50 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2005-11-30
• Study Completion Date: 2005-11-30

Brief Summary

To compare the rate and extent of absorption of griseofulvin from a test formulation of Griseofulvin 125 mg/5 mL Suspension versus the reference Grifulvin V® 125 mg/5 mL Suspension under fasting conditions.

Detailed Description

Study Type: Interventional Study Design: A randomized, two-way crossover, open-label, single-dose, fasting design.

Official Title: A TWO-WAY CROSSOVER, OPEN-LABEL, SINGLE-DOSE, FED, BIOEQUIVALENCE STUDY OF GRISEOFULVIN 125 mg/5 mL SUSPENSION VERSUS GRIFULVIN V® 125 mg/5 mL SUSPENSION IN NORMAL, HEALTHY, NON-SMOKING MALE AND FEMALE SUBJECTS

Further study details as provided by Actavis Elizabeth LLC:

Primary Outcome Measures:

Rate and Extend of Absorption

Conditions

Healthy

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Blinding Strategy: NONE

Study Groups

A

Griseofulvin 125 mg/5 mL Suspension, single dose

Group Type: EXPERIMENTAL

Griseofulvin 125 mg/5 mL Suspension, single dose

Intervention Type: DRUG

A: Experimental Subjects received Alpharma formulated products under fasting conditions

B

Grifulvin V® 125 mg/5 mL Suspension, single dose

Group Type: ACTIVE_COMPARATOR

Grifulvin V® 125 mg/5 mL Suspension, single dose

Intervention Type: DRUG

B: Active comparator Subjects received Ortho Neutrogena formulated products under fasting conditions

Interventions

Griseofulvin 125 mg/5 mL Suspension, single dose

A: Experimental Subjects received Alpharma formulated products under fasting conditions

Intervention Type: DRUG

Grifulvin V® 125 mg/5 mL Suspension, single dose

B: Active comparator Subjects received Ortho Neutrogena formulated products under fasting conditions

Intervention Type: DRUG

Other Intervention Names

Griseofulvin; Griseofulvin

Eligibility Criteria

Inclusion Criteria

1. Non-smoking male or female with a minimum age of 18 years.

2. Body Mass Index (BMI = weight/height2) greater than or equal to 18.5 kg/m2 and less than or equal to 29.9 kg/m2.

3. Normal findings in the physical examination, 12-lead ECG and vital signs (blood pressure between 100-140/60-90 mmHg, heart rate between 50-99 beats/minute, temperature between 35.8°C and 37SC).

4. Negative for drugs of abuse and nicotine.

5. Negative for hepatitis B-surface antigen, hepatitis C and HIV.

6. Female subjects: negative for pregnancy (as evaluated by serum β-CG test).

7. No clinical laboratory values outside of the acceptable range as defined by BCR, unless the Principal Investigator decides that they are not clinically significant.

8. Female subjects who are surgically sterile for at least 6 months or post-menopausal for at least 1 year, or who will avoid pregnancy for at least 10 days before the study, during the study and up until 1 month after the end of the study.

9. Availability of the subject for the entire study period and willingness of the subject to adhere to protocol requirements, as evidenced by a signed ICF.

Exclusion Criteria

1. Known history of hypersensitivity to griseofulvin (e.g. Grifulvin V®, gris-PEG®, Fulvicin®) penicillin, or drugs derived from the same species of Penicillium.

2. Known history or presence of cardiac, pulmonary, gastrointestinal, endocrine, musculoskeletal, neurological, hematological, liver or kidney disease, unless deemed not clinically significant by the Principal Investigator or Sub-investigator.

3. Presence of any significant physical or organ abnormality.

4. Any history or evidence of psychiatric or psychological disease (including depression) unless deemed not clinically significant by the Principal Investigator or Sub-investigator.

5. History of presence of any skin conditions (e.g. dermatitis, eczema, psoriasis).

6. Presence of any skin rashes.

7. Any subject who has been previously diagnosed with porphyria.

8. Any clinically significant illness during the 4 weeks before this study.

9. Any subject who has been treated with any known enzyme-altering drugs such as barbiturates, phenothiazines, cimetidine, carbamazepine, etc., within 30 days prior to the first dose of the study medication.

10. Known history or presence of food allergies, or any condition known to interfere with the absorption, distribution, metabolism or excretion of drugs.

11. Any history of severe allergic reaction (including drugs, food, insect bites, environmental allergens).

12. Significant or recent history of asthma (after 12 years of age).

13. Any subject with a history of drug abuse.

14. Any subject with a recent (less than 1 year) history of alcohol abuse.

15. Use of any prescription medication within 14 days preceding this study.

16. Use of over-the-counter (OTC) medication within 7 days preceding this study (except for spermicidal/barrier contraceptive products).

17. Female subjects: use of contraceptives (oral, emergency [Plan B®], transdermal, implant, Mirena® IUD, NuvaRing®) within 30 days before drug administration or a depot injection of progestogen drug (e.g. Depo-Provera®) within 1 year before drug administration.

18. Female subjects: evidence of pregnancy or lactation.

19. Any subject who has had blood drawn within 56 days preceding this study, during the conduct of any clinical study at a facility other than BCR, or within the lockout period specified by a previous study conducted at BCR.

20. Participation in a clinical trial with an investigational drug within 30 days preceding this study.

21. Any subject who has donated blood within 56 days preceding this study.

22. Any subject who has participated as a plasma donor in a plasmapheresis program within 7 days preceding this study.

23. Any subject who has adhered to a significantly abnormal diet during the 4 weeks preceding the first dose of the study.

24. Intolerance to venipuncture.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Actavis Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Actavis Inc

Principal Investigators

Paul Y. Tam,, MD

Role: PRINCIPAL_INVESTIGATOR

Biovail Contract Research

Locations

Biovail Contract Research (A Division of Biovail Corporation)

Toronto, Ontario, Canada

Countries

Canada

Other Identifiers

3148

Identifier Type: -

Identifier Source: org_study_id