Ibuprofen 4% (w/v) Pivotal Bioequivalence Study

NCT ID: NCT03496324

Last Updated: 2019-06-05

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 24 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2016-02-29
• Study Completion Date: 2016-05-06

Brief Summary

Bioequivalence evaluation of Nurofen for Children® with reference formulation of Algifor® Junior by determining and comparing the rate and extent of absorption in both fed and fasted states

Conditions

Bioequivalence of the Test Formulation

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: BASIC_SCIENCE
• Blinding Strategy: NONE

Study Groups

Test (fed): Nurofen for Children

Nurofen for Children® 400 mg/10 ml by mouth under fed condition

Subjects participated in Treatment Sequence: BACD, DCAB, ADBC and CBDA.

Group Type: ACTIVE_COMPARATOR

Nurofen for Children®

Intervention Type: DRUG

Nurofen for Children® 400 mg/10 ml

Test (fasted): Nurofen for Children

Nurofen for Children® 400 mg/10 ml by mouth under fasted condition.

Subjects participated in Treatment Sequence: BACD, DCAB, ADBC and CBDA.

Group Type: ACTIVE_COMPARATOR

Nurofen for Children®

Intervention Type: DRUG

Nurofen for Children® 400 mg/10 ml

Reference (fed): Algifor Junior

Algifor® Junior 400 mg/20 ml by mouth under fed condition.

Subjects participated in Treatment Sequence: BACD, DCAB, ADBC and CBDA.

Group Type: EXPERIMENTAL

Algifor® Junior

Intervention Type: DRUG

Algifor® Junior 400 mg/20 ml

Reference (fasted): Algifor Junior

Algifor® Junior 400 mg/20 ml by mouth under fasted condition.

Subjects participated in Treatment Sequence: BACD, DCAB, ADBC and CBDA.

Group Type: EXPERIMENTAL

Algifor® Junior

Intervention Type: DRUG

Algifor® Junior 400 mg/20 ml

Interventions

Nurofen for Children®

Nurofen for Children® 400 mg/10 ml

Intervention Type: DRUG

Algifor® Junior

Algifor® Junior 400 mg/20 ml

Intervention Type: DRUG

Other Intervention Names

NfC®; Ibuprofen oral suspension

Eligibility Criteria

Inclusion Criteria

1. Subjects who had given written informed consent.

2. Age: ≥18 years ≤50 years.

3. Sex: Male or female subjects who were eligible for entry.

4. Female subject of childbearing potential with a negative pregnancy test at the screening visit and who were willing to use an effective method of contraception, if applicable (unless of non-childbearing potential or where abstaining from sexual intercourse was in line with the preferred and usual lifestyle of the subject) from first dose until 3 months after the final dose of Investigational Medicinal Product (IMP). Effective forms of contraception included: established use of oral, injected or implanted hormonal methods of contraception, placement of an intrauterine device (IUD) or intrauterine system (IUS), barrier methods of contraception: condom or occlusive cap (diaphragm or cervical/vault caps) with spermicidal foam/gel/film/cream/suppository, male sterilisation (with the appropriate post-vasectomy documentation of the absence of sperm in the ejaculate).

5. Female subject of non-child bearing potential with negative pregnancy test at the screening visit. For the purposes of this study, this was defined as the subject being amenorrheic for at least 12 consecutive months or at least 4 months post-surgical sterilisation (including bilateral fallopian tube ligation or bilateral oophorectomy with or without hysterectomy). Menopausal status was confirmed by demonstrating at screening that levels of follicle stimulating hormone (FSH) fell within the respective pathology reference range. In the event a subject's menopause status had been clearly established (for example, the subject indicated she had been amenorrheic for 10 years), but FSH levels were not consistent with a post-menopausal condition, determination of subject eligibility was at the discretion of the Principal Investigator following consultation with the Sponsor's Responsible Physician.

6. Male subject willing to use an effective method of contraception, if applicable (unless anatomically sterile or where abstaining from sexual intercourse in line with the preferred and usual lifestyle of the subject) from first dose until 3 months after the final dose of IMP.

7. Healthy subjects as determined by past medical history, physical examination, vital signs, electrocardiogram (ECG), and laboratory tests at screening.

8. Healthy subjects with a body mass index (BMI) of ≥20 and ≤27 kg/m2.

Exclusion Criteria

1. Pregnant or lactating females.

2. A history and/or presence of significant disease of any body system, including psychiatric disorders as specified in Chapter 5 of the International Classification of Diseases (ICD) 10.

3. Any condition that may have interfered with the absorption, distribution, metabolism or excretion of drugs.

4. A history of allergy or intolerance (including angioedema, urticaria, bronchospasm and rhinitis) related to treatment with ibuprofen, aspirin or other non-steroidal anti-inflammatory drugs (NSAIDs), or the excipients of the formulations.

5. A history of or active peptic or duodenal ulcers or gastrointestinal bleed or upper gastro-intestinal bleed, or other significant gastro-intestinal disorders.

6. A history of frequent dyspepsia, e.g. heartburn or indigestion.

7. A history of migraine.

8. Users of nicotine products i.e. current smokers and ex-smokers who had smoked within the 6 months prior to dosing with the study medication or users of cigarette replacements (e.g. e-cigarettes, nicotine patches or gums).

9. A history of substance abuse (including alcohol).

10. High consumption of stimulating drinks (coffee, tea, cola, energy drinks etc. total caffeine intake per day above 300 mg (1 cup of coffee equated to 50 mg)).

11. Those with positive screen/test for drugs of abuse including alcohol on any occasion throughout the study.

12. Ingestion of a prescribed drug at any time in the 14 days before dosing with study medication (excluding hormonal contraceptives and hormone replacement therapy), or consumption of enzyme inhibitors or inducers during the previous month (such as barbiturates, carbamazepine, erythromycin, phenytoin, etc.).

13. Ingestion of an over-the-counter preparation within 7 days before dosing with study medication, including herbal medications, vitamin/fish oil supplements, ibuprofen and other NSAID.

14. Donation of blood in quantity >400 mL, e.g., to the blood transfusion service in the previous 12 weeks before enrolment into the study.

15. Known human immune deficiency virus (HIV) positive status, or a positive viral serology screen.

16. Topical use of ibuprofen within 7 days before dosing with IMP.

17. Those previously randomized into this study.

18. Employee at study site.

19. Partner or first degree relative of the Investigator.

20. Those who have participated in a clinical trial in the previous 12 weeks.

21. Those unable, in the opinion of the Investigator, to comply fully with the study requirements.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 50 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Reckitt Benckiser Healthcare (UK) Limited

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Other Identifiers

2015-003894-13

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

RB7-UK-1509

Identifier Type: -

Identifier Source: org_study_id