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Pharmacokinetics of Y-4 Tablets With Pregabalin Capsules and Riluzole Tablets in U.S. Healthy Participants

24. mai 2026 oppdatert av: Neurodawn Pharmaceutical Co., Ltd.

An Open-label, Single-dose, Three-period Phase Ⅰ Study to Compare the Pharmacokinetics of Y-4 Tablets With Pregabalin Capsules and Riluzole Tablets in U.S. Healthy Participants

The primary goal of this clinical trial is to compare pharmacokinetic characteristics of Y-4 tablets with pregabalin capsules and riluzole tablets in the US healthy adult participants after single oral administration under fasted condition.

The secondary goal of the trial is to evaluate the safety and tolerability of Y-4 tablets, pregabalin capsules and riluzole tablets in the US healthy adult participants.

Studieoversikt

Detaljert beskrivelse

This study will be an open-label, single-dose, three-period study in healthy adult participants. A total of at least 10 participants (about half men and half women) will be will be enrolled and needed to complete in the study. Participants enrolled in this study wil be administered with Y-4 tablets, pregabalin capsules and riluzole tablets at three periods with a 7-day washout.

Periods and corresponding treatments are planned as following:

Period 1: Y-4 tablet, one tablet, 112.5 mg/28.125 mg (pregabalin/riluzole) Period 2: pregabalin capsule, one capsule, 75 mg/capsule Period 3: riluzole tablet, one tablet, 50 mg/tablet

Studietype

Intervensjonell

Registrering (Antatt)

11

Fase

  • Fase 1

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Studiesteder

    • New Jersey
      • Secaucus, New Jersey, Forente stater, 07094
        • Frontage Clinical Services,Inc.
        • Ta kontakt med:

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Voksen

Tar imot friske frivillige

Ja

Beskrivelse

Inclusion Criteria:

  1. Healthy adult male and female participants, 18-45 years of age (including both ends).
  2. Body weight ≥ 50 kg for male and ≥ 45 kg for female, body mass index (BMI) within the range of 19 - 28 kg/m2 (including both ends).
  3. During the screening period, serum creatinine is within the normal range, or the standard creatinine clearance (CLcr) estimated by Cockcroft-Gault formula is ≥ 80 mL/min (for female participant, according to the calculation result × 0.85)
  4. Participants who are able to understand and give their signed informed consent before any trial related procedures are performed.

Exclusion Criteria:

  1. Participants who are known to be allergic to pregabalin, riluzole or any excipients of Y-4 tablets (microcrystalline cellulose, copovidone, croscarmellose sodium, colloidal silicon dioxide, magnesium stearate, Opadry amb Ⅱ), have allergic diseases or allergic constitution;
  2. Participants who have special requirements for diet and cannot follow the unified diet;
  3. Physical examinations, vital signs, 12-lead electrocardiograms (ECG), laboratory tests (Hematology, serum chemistry, coagulation test, urinalysis, etc.) and other screening tests found abnormalities that the researchers judged to be of clinical significance;
  4. Participants who have experienced angioedema in the past (such as swelling of the face, mouth (tongue, lips, and gums), and neck (pharynx and throat));
  5. History of dizziness or vertigo with clinical significance, or disease of inner ear known to cause dizziness or vertigo;
  6. QTcF > 450 msec at the screening stage (Corrected using Fridericia's formula: QTcF = QT /(RR^0.33), where RR = 60 / heart rate);
  7. Diagnosed with insomnia, anxiety disorder, depression, epilepsy, or other serious mental disorders, and principal investigator determines that the participant is not suitable to participate in this trial;
  8. Presence or history of hepatic or renal disease or any other condition known to interfere with the absorption, distribution, metabolism or excretion of medicines, participants who have impaired hepatic function at the time of screening: alanine aminotransferase (ALT) or aspartate aminotransferase (AST) > 1.5 ULN; or total bilirubin (TBIL) > 1.0 ULN;
  9. Participants who drink too much tea, coffee and/or caffeine-containing beverages (more than 8 cups, 1 cup = 250 mL) every day within 3 months prior to screening, or disagree that any caffeine-containing beverages are prohibited during the trial;
  10. Participants who have consume any diet (food or beverage) rich in grapefruit, pitaya, mango and cranberry within 14 days prior to screening;
  11. Participants have disease history or current disease that may affect the safety evaluation of the participant or the internal process of the study drug, including the central nervous system, cardiovascular system, digestive system, endocrine system, respiratory system, urinary system, hematological system, immunology, psychiatry, metabolic abnormalities, gastrointestinal surgery (excluding appendicitis surgery), etc. In particular, there is a history of dysphagia or any gastrointestinal disease affecting drug absorption (including frequent nausea or vomiting caused by any cause) and eye diseases;
  12. Donation or loss of blood equal to or in excess of 400 mL, or blood transfusion within 3 months prior to screening; or donation or loss of blood equal to or in excess of 200 mL within 1 month prior to screening;
  13. Participants who have taken any drugs known to be strong inhibitors or inducers of cytochrome P450 enzymes within 2 months prior to screening (such as inducers - barbiturates, carbamazepine, phenytoin, glucocorticoids, omeprazole; inhibitors - serotonin reuptake inhibitors (SSRI) antidepressants, cimetidine, diltiazem, macrolides, nitroimidazoles, sedative hypnotics, verapamil, fluoroquinolones, antihistamines); or participants who have taken any prescription drugs, over-the-counter drugs and traditional Chinese medicine or herbal medicine other than the above drugs within 14 days prior to screening;
  14. Participants who have taken central nervous system (CNS) depressants including opioids (pethidine hydrochloride, morphine, dihydromorphine hydrochloride, fentanyl, Tramadol, etc), benzodiazepines (diazepam, flurazepam, clonazepam, oxazepam, chlordiazepine and triazolam etc), antiepileptic drugs (carbamazepine, sodium valproate, phenobarbital drugs etc) within 2 months prior to screening;
  15. Participant with sleep apnea, or participants with severe sleep snoring and daytime drowsiness;
  16. Participants with history of neuropsychiatric disorders, including current or past history of mental illness, suicidal ideation based on the C-SSRS score of 1 or higher;
  17. Participant participated in any other clinical trials within 3 months prior to screening;
  18. Current or former drug users, or positive urine screen for drugs of abuse at screening (screening items include: Opiates, Amphetamines, Cocaine, Cannabinoids, Barbiturates, Benzodiazepines);
  19. Alcoholics or regular drinkers within 3 months prior to screening, that is, those who drink more than 14 units of alcohol per week (1 unit = 360 mL of beer or 45 mL of alcohol with 40% alcohol content or 150 mL of wine), or whose alcohol breath test results are greater than 0.0 mg/100 mL, or who cannot abstain from alcohol during the trial;
  20. Smokers or those who cannot comply with the prohibition of smoking during the trial, or positive for cotinine screening;
  21. Participants who is positive for hepatitis B surface antigen (HBsAg), hepatitis C virus (HCV) antibody, syphilis antibody or human immunodeficiency virus (HIV) antibody;
  22. Male participants (or their partners) or female participants have baby plans during the whole trial period and within 3 months after the end of the trail, or participants are unwilling to take one or more non-drug contraceptive measures (such as complete abstinence, condoms, ligation, etc.) during the trial period.
  23. Female participants who have unprotected intercourse within 14 days prior to screening, or pregnant or lactating women;
  24. Participants with poor compliance or other factors unsuitable for participation in this trial.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Ikke-randomisert
  • Intervensjonsmodell: Sekvensiell tildeling
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Y-4 tables
In the morning of Day 1 ,single oral administration one Y-4 tablet in the state of fasting state.
Participants will be admitted to research center on Day-1. Participants are required to fast for at least 10 hours prior to dosing on Day 1. In the morning of Day 1, participants will be administered with one tablet of Y-4 (pregabalin 112.5 mg and riluzole 28.125 mg), then participants will be monitored and blood samples will be collected for the following 72 hours (Day4).
Eksperimentell: Pregabalin capsule
In the morning of Day 8 ,single oral administration one pregabalin capsule in the state of fasting state.
Participants are required to fast for at least 10 hours prior to dosing on Day 8. In the morning of Day 8, participants will be administered with one pregabalin capsule (75 mg pregabalin), then participants will be monitored and blood samples will be collected for the following 72 hours (Day 11).
Eksperimentell: Riluzole tablet
In the morning of Day 15 ,single oral administration one riluzole tablet in the state of fasting state.
Participants are required to fast for at least 10 hours prior to dosing on Day 15. In the morning of Day 15, participants will be administered with one riluzole tablet (50 mg riluzole), then participants will be monitored and blood samples will be collected for the following 72 hours (Day 18).

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Cmax
Tidsramme: On Day1-4、Day8-11、Day15-18 of observation period.
Maximum observed concentration, it was obtained directly from the measured plasma concentration-time data;
On Day1-4、Day8-11、Day15-18 of observation period.
AUC0-t
Tidsramme: On Day1-4、Day8-11、Day15-18 of observation period.
Area under the concentration-time curve from time zero to the last detectable concentration
On Day1-4、Day8-11、Day15-18 of observation period.
AUC0-∞
Tidsramme: On Day1-4、Day8-11、Day15-18 of observation period.
Area under the concentration-time curve from time 0 to infinity (extrapolated).
On Day1-4、Day8-11、Day15-18 of observation period.

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Tmax
Tidsramme: On Day1-4、Day8-11、Day15-18 of observation period.
Time of observed Cmax, it was obtained directly from the measured plasma concentration-time data;
On Day1-4、Day8-11、Day15-18 of observation period.
λz
Tidsramme: On Day1-4、Day8-11、Day15-18 of observation period.
Terminal-phase elimination rate constant, slope of curves terminal segment at semi-log concentration-time curve calculated by linear regression;
On Day1-4、Day8-11、Day15-18 of observation period.
t1/2
Tidsramme: On Day1-4、Day8-11、Day15-18 of observation period.
Terminal elimination half-life
On Day1-4、Day8-11、Day15-18 of observation period.
CL/F
Tidsramme: On Day1-4、Day8-11、Day15-18 of observation period.
Apparent total body clearance
On Day1-4、Day8-11、Day15-18 of observation period.
Vz/F
Tidsramme: On Day1-4、Day8-11、Day15-18 of observation period.
Apparent volume of distribution
On Day1-4、Day8-11、Day15-18 of observation period.
MRT0-t
Tidsramme: On Day1-4、Day8-11、Day15-18 of observation period.
Mean residence time within the time from time zero to the lowest testing plasma concentration
On Day1-4、Day8-11、Day15-18 of observation period.
MRT0-∞
Tidsramme: On Day1-4、Day8-11、Day15-18 of observation period.
Mean residence time extrapolated from zero to infinity
On Day1-4、Day8-11、Day15-18 of observation period.
AUC_%Extrap
Tidsramme: On Day1-4、Day8-11、Day15-18 of observation period.
The percentage of the AUC0-inf that has been extrapolated.
On Day1-4、Day8-11、Day15-18 of observation period.
The Incidence of subject getting abnormal results of clinical adverse events after treatment.
Tidsramme: From the first day to the 25th± 1st day after the start of administration
An AE is defined as any untoward medical event that occurs after receiving a drug or treatment or any deterioration of a disease or symptom that existed before receiving the investigational product or treatment (excluding the disease studied in this trial) in a subject or a clinical investigation subject, whether or not considered related to the investigational product or treatment. All AEs will be coded using the MedDRA, and summarized by SOC and PT. Number and percentage of participants with AEs,SAEs, and AEs that lead to early withdrawal will be summarized. AEs might be summarized by severity (grade) and relationship to investigational product if judged appropriate.
From the first day to the 25th± 1st day after the start of administration
The Incidence of subject getting abnormal results of laboratory tests after treatment.
Tidsramme: From the first day to the 25th± 1st day after the start of administration
Record changes from baseline to post-treatment, listing deviations from normal ranges post-treatment.Clinical laboratory examinations including hematology, serum chemistry, ,urinalysis,coagulation test (PT/APTT/FIB/TT).Normal range is provided by the site.
From the first day to the 25th± 1st day after the start of administration
The Incidence of subject getting abnormal results of 12-lead electrocardiograms after treatment.
Tidsramme: From the first day to the 25th± 1st day after the start of administration
Record changes from baseline to post-treatment, listing deviations from normal ranges post-treatment.Standard ECG parameters will be measured including RR, PR, and QTc intervals, and QRS duration .Normal range is provided by the site.
From the first day to the 25th± 1st day after the start of administration
The Incidence of subject getting abnormal results of vital signs after treatment
Tidsramme: From the first day to the 25th± 1st day after the start of administration
Record changes from baseline to post-treatment, listing deviations from normal ranges post-treatment.Vital signs, including blood pressure (sitting position), pulse rate, temperature (frontal temperature, Celsius), and respiration.Normal range is provided by the site.
From the first day to the 25th± 1st day after the start of administration
The Incidence of subject getting abnormal results of blood oxygen saturation after treatment.
Tidsramme: From the first day to the 25th± 1st day after the start of administration
Record changes of blood oxygen saturation from baseline to post-treatment, listing deviations from normal ranges post-treatment. Normal range is provided by the site
From the first day to the 25th± 1st day after the start of administration
The Incidence of subject getting abnormal results of physical examinations after treatment.
Tidsramme: From the first day to the 25th± 1st day after the start of administration
Record changes from baseline to post-treatment, listing deviations from normal ranges post-treatment. The physical examinations will consist of a general assessment, dermatologic, lymph nodes, head, eyes, ears, nose, throat, chest, neck, thyroid gland, cardiac, lung, chest (included breast), abdomen, extremities, musculoskeletal, neurologic, and other physical findings of note. Normal range is provided by the site.
From the first day to the 25th± 1st day after the start of administration
The Incidence of subject getting abnormal results of C-SSRS scale evaluation after treatment.
Tidsramme: From the first day to the 25th± 1st day after the start of administration
Record changes of C-SSRS scale evaluation from baseline to post-treatment.
From the first day to the 25th± 1st day after the start of administration

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

30. juni 2026

Primær fullføring (Antatt)

31. august 2026

Studiet fullført (Antatt)

31. oktober 2026

Datoer for studieregistrering

Først innsendt

24. mai 2026

Først innsendt som oppfylte QC-kriteriene

24. mai 2026

Først lagt ut (Faktiske)

1. juni 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

1. juni 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

24. mai 2026

Sist bekreftet

1. mai 2026

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Ja

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

produkt produsert i og eksportert fra USA

Ja

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