Bioequivalence Study of Perampanel Tablets 10 mg

Epilepsy Clinical Trial

Official title:

An Open-label, Balanced, Randomized, Two Treatment, Two Sequence, Two Period, Two Way Cross-over, Single Dose Bioequivalence Study of Perampanel Tablets 10 mg of Humanis Sağlık A.Ş., Turkey and Fycompa 10 mg Film-coated Tablets of Eisai GmbH Edmund-Rumpler-Straße 3 60549 Frankfurt am Main Deutschland in Normal, Healthy, Adult, Human Subjects Under Fasting Condition

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT06450236
• Other study ID #: PR/BE/23/228
• Status: Completed
• Phase: Phase 1
• Start date: November 22, 2023
• Est. completion date: February 6, 2024

Study information

• Verified date: June 2024
• Source: Humanis Saglik Anonim Sirketi
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

An open-label, balanced, randomized, two treatment, two sequence, two period, two way cross-over, single dose bioequivalence study of Perampanel Tablets 10 mg of Humanis Sağlık A.ġ., Turkey and Fycompa 10 mg film-coated tablets of Eisai GmbH Edmund-Rumpler-Straße 3 60549 Frankfurt am Main Deutschland in normal, healthy, adult, human subjects under fasting condition.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 30
• Est. completion date: February 6, 2024
• Est. primary completion date: November 26, 2023
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 45 Years

Eligibility

Inclusion Criteria:

• Subjects fulfilling the following criteria were included in the study:

• Willing to provide written informed consent for participation in the study, and an ability to comprehend the nature and purpose of the study;

• Willing to be available for the entire study period and to comply protocol requirements;

• Normal, healthy, adult, human subject of 18-45 years (both inclusive) of age;

• Body mass index in the range of 18.50 - 30.00 kg/m2 (both inclusive);

• Normal health status as determined by baseline medical and medication history, at the time of screening and vital signs measurements and physical examination at the time of screening as well as check-in of each study period;

• Normal or clinically non-significant laboratory values as determined by hematological, biochemistry tests and urine analysis;

• Normal or clinically non-significant 12-lead ECG recording;

• Non-smokers and willing to abstain from chewing any tobacco containing products at least 72.00 hours prior to check-in until last sample collection in each study period;

• Non Alcoholic;

• Willing to abstain from xanthine or its derivative containing food or beverages (e.g. chocolates, tea, coffee or cola drinks), at least 48.00 hours prior to check-in until last sample collection in each study period;

• Willing to abstain from grapefruit or its juice at least 72.00 hours prior to check-in until last sample collection in each study period;

• For female subjects:

• Negative urine pregnancy test during screening and negative serum ß-hCG test at the time of check-in of each study period;

• Female subjects with child bearing potential or those within their first two years of onset of menopausal syndrome willing to either abstain from sexual intercourse, or should use of acceptable birth control methods for at least 15 days before 1st check-in till 15 days post lastdose / entire study period. [Acceptable birth control methods include barrier methods such as diaphragm/condom with or without spermicide or surgically sterile (bilateral tubal ligation, bilateral oophorectomy or hysterectomy has been performed)].

Exclusion Criteria:

• Subjects with the following criteria were excluded from the study:

• Any medical or surgical conditions, which might significantly interfere with the functioning of gastrointestinal tract and of blood forming organs;

• Significant history or current evidence of malignancy or chronic - infectious, cardiovascular, renal, hepatic, ophthalmic, pulmonary, neurological, metabolic (endocrine), hematological, gastrointestinal, dermatological, immunological or psychiatric diseases, or organ dysfunction;

• Any major illness or hospitalized within 90 days prior to the first check-in;

• Requiring medication for any ailment having enzyme-modifying activity within one month prior to first check-in and throughout the study;

• Use of any depot injection or an implant of any drug within 3 months prior to first check-in and throughout the study;

• History or presence of galactose intolerance, Lapp lactase deficiency or glucose-galactose malabsorption.

• History of Severe cutaneous adverse reactions (SCARs) including drug reaction with eosinophilia and systemic symptoms(DRESS) and Stevens - Johnson Syndrome (SJS).

• Use of any prescribed medication (including herbal medicines and vitamin supplements) or OTC products within 30 days prior to first check-in and throughout the study;

• History or presence of significant gastric and/or duodenal ulceration;

• Difficulty in swallowing tablets or capsules;

• Use of any recreational drug or history of drug addiction;

• Participated in any clinical investigation requiring repeated blood sampling or have donated blood in past 90 days prior to first check-in;

• Positive urine alcohol and urine drug of abuse tests during check-in of each study period;

• Reactive test for Human Immunodeficiency Virus (HIV) type I/II antibodies or Hepatitis B surface antigen (HBsAg) or Hepatitis C virus antibodies;

• Lactating or nursing female subjects;

• Female subjects using hormonal contraceptive (either oral/implants);

• History of allergy or hypersensitivity intolerance to perampanel or its formulation excipients which, in the opinion of a clinical investigator, would compromise the safety of the subject or the study;

• History of difficulty in accessibility of veins in arms.

Related Conditions & MeSH terms

• Epilepsy

Intervention

Drug:
• Perampanel 10 MG
1 tablet of Perampanel Tablets 10mg
• Fycompa 10Mg Tablet
1 tablet of Perampanel Tablets 10mg

Locations

Country	Name	City	State
India	Raptim Research Pvt. Ltd.,	Navi Mumbai

Sponsors (1)

Lead Sponsor	Collaborator
Humanis Saglik Anonim Sirketi

Country where clinical trial is conducted

India, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Maximum concentration obtained (Cmax)	two-sided 90% CI for the test to reference ratio of the population means is within 80.00% to 125.00% for each of the Ln-transformed data Cmax	23 hours
Primary	AUC from time 0 to last collection time 72 (AUC0-72)	two-sided 90% CI for the test to reference ratio of the population means is within 80.00% to 125.00% for each of the Ln-transformed data AUC0-72	23 hours
Secondary	Time of the maximum measured plasma concentration (Tmax)	Description Statistics	23 hours