Bioequivalence Evaluation of a New and Current Tablet of ASP015K

NCT ID: NCT02531191

Last Updated: 2024-10-16

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1
• Total Enrollment: 40 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2015-06-21
• Study Completion Date: 2015-07-15

Brief Summary

The objective of this study is to evaluate the bioequivalence of a new tablet versus a current tablet of ASP015K under fasting conditions after single oral administration in healthy male subjects.

Detailed Description

This is an open-label, randomized, single dose, 2-way crossover designed study. Forty non-elderly healthy male subjects will receive an ASP015K small tablet or an ASP015K current tablet in each period under fasted conditions. If the bioequivalence between two tablets cannot be demonstrated because of an insufficient number, an add-on subject study will be conducted as needed. The design of the add-on subject study will be the same with that of the initial study.

Conditions

Healthy Volunteers

Study Design

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

Study Groups

New Tablet Preceding Group

Each subject received an ASP015K small tablet in period 1 and an ASP015K current tablet in period 2 under fasted conditions with 200 mL of water.

Group Type: EXPERIMENTAL

peficitinib

Intervention Type: DRUG

oral

Current Tablet Preceding Group

Each subject received an ASP015K current tablet in period 1 and an ASP015K small tablet in period 2 under fasted conditions with 200 mL of water.

Group Type: EXPERIMENTAL

peficitinib

Intervention Type: DRUG

oral

Interventions

peficitinib

oral

Intervention Type: DRUG

Other Intervention Names

ASP015K

Eligibility Criteria

Inclusion Criteria

• 50.0 kg ≤ body weight at screening < 80.0 kg
• 17.6 ≤ BMI at screening < 26.4 [BMI = Body weight (kg) / (Body height (m))2]
• Subjects who agree to use the following highly effective contraception consisting of two forms of birth control (at least one of which must be a barrier method) starting at written informed consent through 90 days after the study drug administration in Period 2.
• Subjects who agree not to donate sperm starting at informed consent through 90 days after the study drug administration in Period 2.
• Subjects judged as healthy by investigator or sub-investigator based on physical examinations (subjective symptoms and objective findings) and all clinical tests obtained at screening and from check-in to immediately before the study drug administration in Period 1.

Exclusion Criteria

• Subjects who have received investigational drugs within 120 days prior to screening or who plan to receive investigational drugs from screening assessment to check-in in Period 1 (Day -1).
• Any blood donation or blood drawing apply the following:

• Whole blood collection (≥ 400 mL): from 90 days prior to screening to check-in in Period 1 (Day -1)
• Whole blood collection (≥ 200 mL): from 30 days prior to screening to check-in in Period 1 (Day -1)
• Platelet or plasma donation: from 30 days prior to screening to check-in in Period 1 (Day -1)
• Subjects who had used or plan to use any prescribed or non-prescribed drugs within 7 days prior to check-in in Period 1 (Day -1).
• Any deviation of blood pressure, pulse, body temperature, or 12-lead ECG at screening or check-in in Period 1 (Day -1) from the following normal range:

• Supine pressure: Systolic: ≥ 90 mmHg, ≤ 140 mmHg; Diastolic: ≥ 40 mmHg, ≤ 90 mmHg
• Supine pulse: ≥ 40 bpm, ≤ 99 bpm
• Axillary temperature: ≥ 35.0 ºC, ≤ 37.0 ºC
• 12-lead ECG: Normal or clinically irrelevant abnormality QTc interval: ≥ 330 msec, < 430 msec
• Any deviation of laboratory tests at Screening or on Day -1 (check-in) in Period 1 from the following normal range. Normal range of each test at the test or assay site will be used.

• Hematology: > 20% of upper limit or < 20% of lower limit.
• Chemistry: deviation of ALT, AST, Cre, blood electrolytes (Na, K, Cl), or fasting blood glucose. > 20% of upper limit or < 20% of lower limit in other than above tests; however no lower limit is set with respect to ALT, AST, γ-GTP, T-Bil, ALP, LDH, CK, T-Cho, TG, Cre, and UA.
• Urinalysis (qualitative): deviation in any of the urinalysis.
• Urinary drug abuse test: positive for benzodiazepines, cocaine-based narcotics, analeptic drugs, cannabis, barbituric acid derivatives, morphine-based narcotics, phencyclidines, or tricyclic antidepressants.
• Immunological test: positive for HBs antigen, HBc antibody, HCV antibody, HIV antigen or antibody, or syphilis.
• Subjects who have any history or complication of drug allergies.
• Subjects who have a history of upper gastrointestinal symptoms, i.e. nausea, vomit, stomach ache, etc. within 7 days prior to check-in in Period 1 (Day -1).
• Subjects who have any history or complication of hepatic disease, i.e. viral hepatitis, drug induced liver injury, hepatic dysfunction, etc.
• Subjects who have any history or complication of cardiac disease, i.e. congestive heart failure, angina, arrhythmia requires a treatment, etc.
• Subjects who have any history or complication of respiratory disease, i.e. bronchial asthma, chronic bronchitis, pneumonitis, etc. (except for a history of asthma in childhood)
• Subjects who have any history or complication of gastrointestinal disease, i.e. peptic ulcer, reflux esophagitis, etc. (except for a history of appendicitis)
• Subjects who have any history of gastrointestinal resection (except for a history of appendectomy)
• Subjects who have any history or complication of renal disease, i.e. acute renal failure, glomerulonephritis, intestinal nephritis, etc.
• Subjects who have any history or complication of endocrine disease, i.e. hyperthyroidism, abnormality of growth hormone, etc.
• Subjects who have any history or complication of cerebrovascular disorder, i.e. cerebral infarction.
• Subjects who have any history or complication of malignant tumor.
• Subjects who have any history or complication of congenital short QT syndrome.
• Subjects who have any history or complication of lymphatic disease, i.e. lymphoproliferative disease.
• Subjects any of the following apply regarding tuberculosis:

• History of active tuberculosis
• Abnormality in chest X-ray test at screening
• Contact with patients with infectious tuberculosis
• Subjects any of the following apply regarding infectious disease other than tuberculosis:

• History or complication of serious herpes zoster or disseminated herpes zoster
• More than once relapse of localized herpes zoster
• Hospitalization due to serious infection within 90 days before check-in in Period 1 (Day -1)
• I.V. antibiotics treatment within 90 days before check-in in Period 1 (Day -1) (except for prevention use)
• Judged as prone to infections by investigator or sub-investigator, i.e. subjects with urethral catheterization.
• Subjects who have any history of inoculation of live vaccine or attenuated live vaccine within 56 days prior to check-in in Period 1 (Day -1).
• Subjects who have any history of clinically serious allergy (Clinically serious allergy; allergy induced systemic urticaria or anaphylactic shock require hospitalization when exposed to specific antigens or drugs).
• Subjects who have any history or complication of heart failure classified as NYHA Class III or IV.
• Subjects who have a history of ASP015K administration.
• Subjects with excessive alcohol drinking or smoking.

• Criteria for "excessive":

1. Smoking: ≥ 20 cigarettes/day

2. Alcohol drinking: ≥ 45 g/day (a large bottle of beer contains 25 g of alcohol, 1 gou of Japanese sake contains 22 g of alcohol)

• Employee of the sponsor, CROs or study site involved in this study.
• Subjects judged as inappropriate for the study by investigator or sub-investigators.

• Minimum Eligible Age: 20 Years
• Maximum Eligible Age: 44 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: Yes

Sponsors

Astellas Pharma Inc

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Medical Director

Role: STUDY_DIRECTOR

Astellas Pharma Inc

Locations

Tokyo, , Japan

Countries

Japan

References

Toyoshima J, Shibata M, Kaibara A, Kaneko Y, Izutsu H, Nishimura T. Population pharmacokinetic analysis of peficitinib in patients with rheumatoid arthritis. Br J Clin Pharmacol. 2021 Apr;87(4):2014-2022. doi: 10.1111/bcp.14605. Epub 2020 Dec 1.

Reference Type: DERIVED

PMID: 33068028 (View on PubMed)

Shibata M, Toyoshima J, Kaneko Y, Oda K, Kiyota T, Kambayashi A, Nishimura T. The Bioequivalence of Two Peficitinib Formulations, and the Effect of Food on the Pharmacokinetics of Peficitinib: Two-Way Crossover Studies of a Single Dose of 150 mg Peficitinib in Healthy Volunteers. Clin Pharmacol Drug Dev. 2021 Mar;10(3):283-290. doi: 10.1002/cpdd.843. Epub 2020 Jul 3.

Reference Type: DERIVED

PMID: 32618438 (View on PubMed)

Other Identifiers

015K-CL-PK27

Identifier Type: -

Identifier Source: org_study_id