Bioequivalence Study of Aripiprazole From Apipe 10 mg Orally Disintegrating Tablets (Man. by: P&C Labs (Pellets & CR Products), Egypt) Versus Abilify 10 mg Orodispersible Tablets (Otsuka Pharmaceutical Netherlands B.V., Netherlands)

• Status: Completed
• Trial end date: 2022-12-19
• Target enrollment: 0
• Participant gender: Male

Summary

Comparative randomized, single dose, two-way crossover bioequivalence study to determine the bioequivalence of Aripiprazole from Apipe 10 mg orally disintegrating tablets (Man. by: P&C Labs (Pellets&CR Products), Egypt) versus Abilify 10 mg orodispersible tablets (Otsuka Pharmaceutical Netherlands B.V., Netherlands ) in Healthy Human Volunteers Under Fasting Condition

• Phase: Phase 1
• Accepts Healthy Volunteers?: Accepts Healthy Volunteers

Details

• Lead Sponsor: Genuine Research Center, Egypt
• Collaborator: P&C Labs, Egypt
• Treatments: Aripiprazole

Criteria

Inclusion Criteria:

1. Healthy male, age 45 to 55 years, inclusive.

2. Body weight within 15% of normal range according to the accepted normal values for body mass index (BMI).

3. Medical demographics without evidence of clinically significant deviation from normal medical condition.

4. Results of clinical laboratory test are within the normal range or with a deviation that is not considered clinically significant by principal investigator.

5. Fully informed subjects that consented to participate in the study.

6. Subject does not have allergy to the drugs under investigation.

Exclusion Criteria:

1. Females

2. Subjects with a prior personal or family history of dystonic reactions to medications.

3. Subjects with known allergy or any contraindications to the products tested.

4. Heavy smokers (more than 10 cigarettes per day).

5. Subjects that do not agree not to consume alcohol-containing beverages and foods for 48 hours before dosing and throughout the period of sample collection

6. Subjects whose values of BMI were outside the accepted normal ranges.

7. Medical demographics with evidence of clinically significant deviation from normal medical condition.

8. Results of laboratory tests which are clinically significant.

9. Acute infection within one week preceding first study drug administration.

10. History of drug or alcohol abuse.

11. Subject does not agree not to take any prescription or non-prescription drugs within two weeks before first study drug administration and until the end of the study.

12. Subject is on a special diet (for example subject is vegetarian).

13. Subject does not agree not to consume any beverages or foods containing methyl-xanthenes e.g. caffeine (coffee, tea, cola, chocolate etc.) 48 hours prior to the study administration of either study period until donating the last sample in each respective period.

14. Subject does not agree not to consume any beverages or foods containing grapefruit 7 days prior to first study drug administration until the end of the study.

15. Subject has a history of severe diseases which have direct impact on the study.

16. Participation in a bioequivalence study or in a clinical study within the last 8 weeks before first study drug administration.

17. Subject intends to be hospitalized within 3 months after first study drug administration.

18. Subjects who have blood donated or lost more than 500 mL blood within 3 months prior to the study.