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A Pharmacokinetic Study of Budesonide Delayed Release Tablet D23A (D23) in Healthy Chinese Participants Under Fasting Conditions

3. november 2026 oppdatert av: Triastek, lnc.

A Single-Center, Randomized, Open-Label, Three-Period, Three-Sequence Crossover, Comparative Pharmacokinetic Study of Budesonide Delayed Release Tablet D23A (D23) in Healthy Chinese Participants Under Fasting Conditions

The goal of this clinical trial is to evaluate the PK characteristics and relative bioavailability of single oral doses of Budesonide Delayed Release Tablet and Budesonide Delayed Release Capsules in healthy participants, and to compare the formulation similarity of Budesonide Delayed Release Tablet T1 and T2. The main questions it aims to answer are:

How do the pharmacokinetic (PK) characteristics and relative bioavailability of Budesonide Delayed Release Tablet T1 (strength: 4 mg) compare with those of Budesonide Delayed Release Capsules R (trade name: Nefecon, strength: 4 mg)? How do the PK characteristics and relative bioavailability of Budesonide Delayed Release Tablet T2 (strength: 16 mg) compare with those of Budesonide Delayed Release Capsules R (trade name: Nefecon, strength: 4 mg)? How similar are the formulations of Budesonide Delayed Release Tablet T1 (strength: 4 mg) and T2 (strength: 16 mg), and how do their relative bioavailabilities compare? Researchers will compare Budesonide Delayed Release Tablet T1 (strength: 4 mg) and T2 (strength: 16 mg) to Budesonide Delayed Release Capsules R (trade name: Nefecon, strength: 4 mg) to see if the tablets work to treat primary immunoglobulin A nephropathy (IgAN).

Participants will:

Take a single oral dose of Budesonide Delayed Release Tablet T1 (16 mg, given as 4 mg/tablet × 4 tablets), Tablet T2 (16 mg, given as 16 mg/tablet × 1 tablet), or Capsules R (16 mg, given as 4 mg/capsule × 4 capsules) as directed Visit the clinic regularly for checkups and tests Report any medical problems they experience while taking the study drug

Studieoversikt

Studietype

Intervensjonell

Registrering (Antatt)

18

Fase

  • Fase 1

Kontakter og plasseringer

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

Studiesteder

    • Jiangsu
      • Suzhou, Jiangsu, Kina, 215004
        • The Second Affiliated Hospital of Soochow University

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

18 år og eldre (Voksen, Eldre voksen)

Tar imot friske frivillige

Ja

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

Inclusion Criteria:

1 . Fully understand the purpose, nature, procedures of the study and possible adverse reactions, voluntarily participate in the study, and sign the informed consent form (ICF) before any study procedures begin; 2. Healthy male or female participants aged ≥18 years; 3. Male weight ≥ 50.0 kg, female weight ≥ 45.0 kg; body mass index (BMI) in the range of 18.5 to 24.9 kg/m2 (inclusive); 4. Participants voluntarily agree to use effective contraception during the study and for 3 months after the last dose, and have no plans to conceive or father a child, donate sperm, or donate eggs during that period; 5. Able to communicate well with the investigator and understand and comply with all requirements of this study.

Exclusion Criteria:

  1. Allergic diathesis, a clinical history of allergies to food, drugs, etc., or a known history of allergy to budesonide or to any excipient of either Budesonide Delayed Release Tablet or Budesonide Delayed Release Capsules;

  2. History of chronic or serious diseases of the cardiovascular, hepatic, renal, biliary, respiratory, hematologic and lymphatic, endocrine, immune, psychiatric, or neuromuscular systems within one year prior to screening until randomization;

  3. History of gastrointestinal diseases (including current) from one year prior to screening until randomization, including chronic or active upper gastrointestinal diseases such as esophageal disorder, gastritis, duodenitis, gastrointestinal ulceration, or active gastrointestinal hemorrhage or gastrointestinal surgery;

  4. Have had or currently have infectious diseases within 1 month prior to screening, including fungal/bacterial/viral/parasitic infections, ocular herpes simplex, varicella, measles, etc.;

  5. Have a history of or currently have eye disorders (such as glaucoma, cataracts), or have a family history of glaucoma;

  6. Have clinically significant abnormal results in vital signs, physical examination, clinical laboratory tests (hematology, urinalysis, clinical chemistry, 4-item coagulation test, 4-item infectious disease test) and ECG at screening, as judged by the investigator;

  7. Have had acute diseases within 2 weeks prior to screening until randomization (including acute appendicitis, acute gastroenteritis, acute cerebral infarction, cerebral hemorrhage, angina pectoris, upper gastrointestinal hemorrhage, etc.);

  8. Have the following ECG findings at screening: prolonged QTcF interval (QTcF>450 ms for males, >470 ms for females);

  9. Have used any drugs (including any prescription drugs, over-the-counter drugs, Chinese herbal preparations) or health supplements from 2 weeks prior to screening until randomization;

  10. Have undergone major surgery (excluding diagnostic surgery) from 6 months prior to screening until randomization, or have undergone surgery that, in the investigator's judgment, would affect the absorption, distribution, metabolism, or excretion of the drug, or are planning to undergo surgery during the study;

  11. Have an average weekly alcohol use of more than 14 units (1 unit = 360 mL of 5% alcohol beer or 45 mL of 40% alcohol spirits or 150 mL of 12% alcohol wine) from 3 months prior to screening until randomization, or are unable to abstain from alcohol during the study, or have an alcohol breath test result greater than 0.0 mg/100 mL;

  12. Have consumed tea, coffee, or beverages containing caffeine or alcohol from 48 hours before the first dose until randomization, or are unable to stop consuming them during the study;

  13. Have consumed foods or beverages that affect drug metabolism, such as chocolate, dragon fruit, mango, carambola, guava, pomelo, orange, grapefruit or grapefruit products, from 48 hours before the first dose until randomization, or are unable to stop consuming them during the study;

  14. Have received any vaccine from 4 weeks prior to screening until randomization, or plan to receive any vaccine during the study (by inquiry);

  15. Have participated in any drug or device clinical study from 3 months prior to screening until randomization (participation is defined as receiving the investigational drug or device, and the end time is defined as the date of discharge from the last clinical study);

  16. Have a history of blood donation from 3 months prior to screening until randomization, or have a total blood loss of 400 mL or more from blood donation or other reasons within 6 months (excluding menstrual blood loss for females), or plan to donate blood within 6 months after the last blood collection;

  17. Have an average daily smoking of more than 5 cigarettes from 3 months prior to screening until randomization, or are unable to stop using any tobacco products during the study;

  18. Have a history of drug addiction or drug abuse (including non-medical use of various narcotic drugs and psychotropic drugs);

  19. Have a positive result for any item in the urine drug screen (including: morphine, methamphetamine (ice), ketamine (K powder), ecstasy (MDMA), marijuana (tetrahydrocannabinolic acid), etc.);

  20. Have difficulty with venipuncture or poor vascular conditions, or cannot tolerate venipuncture/indwelling needle, or have a history of fainting from needles or blood;

  21. Have special dietary requirements, or are unable to accept the standardized diet during the study;

  22. Have dysphagia;

  23. Be unsuitable for enrollment or other situations where the participant is unable to participate for personal reasons as judged by the investigator.

    Female participants who meet the following conditions, in addition to the above requirements, should also be excluded:

  24. Have used oral contraception from 30 days prior to screening until randomization;

  25. Have used long-acting estrogen or progesterone injections (including progesterone-releasing intrauterine devices) or implants from 6 months prior to screening until randomization;

  26. Have had unprotected sexual intercourse with a partner from 14 days prior to screening until randomization;

  27. Have a positive pregnancy test;

  28. Are women who are pregnant or lactating.

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: Randomisert
  • Intervensjonsmodell: Crossover-oppdrag
  • Masking: Ingen (Open Label)

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Cmax
Tidsramme: up to 48 hours post-dose

Primary PK parameters

up to 48 hours post-dose
AUC4-t
Tidsramme: up to 48 hours post-dose

Primary PK parameters

up to 48 hours post-dose
AUC0-t
Tidsramme: up to 48 hours post-dose

Primary PK parameters

up to 48 hours post-dose
AUC0-∞
Tidsramme: up to 48 hours post-dose

Primary PK parameters

up to 48 hours post-dose
Tmax
Tidsramme: up to 48 hours post-dose

Secondary PK parameters

up to 48 hours post-dose
Tlag
Tidsramme: up to 48 hours post-dose

Secondary PK parameters

up to 48 hours post-dose
AUC0-4
Tidsramme: up to 4 hours post-dose

Secondary PK parameters

up to 4 hours post-dose
t1/2
Tidsramme: up to 48 hours post-dose

Secondary PK parameters

up to 48 hours post-dose
λz
Tidsramme: up to 48 hours post-dose

Secondary PK parameters

up to 48 hours post-dose
AUC %Extrap
Tidsramme: up to 48 hours post-dose

Secondary PK parameters

up to 48 hours post-dose
CL/F
Tidsramme: up to 48 hours post-dose

Secondary PK parameters

up to 48 hours post-dose
VZ/F
Tidsramme: up to 48 hours post-dose

Secondary PK parameters

up to 48 hours post-dose

Sekundære resultatmål

Resultatmål
Tidsramme
Incidence of adverse events (AEs)
Tidsramme: Through study completion, an average of 13 days
Through study completion, an average of 13 days

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 (Faktiske)

3. november 2026

Primær fullføring (Antatt)

1. januar 2027

Studiet fullført (Antatt)

1. januar 2027

Datoer for studieregistrering

Først innsendt

3. november 2026

Først innsendt som oppfylte QC-kriteriene

3. november 2026

Først lagt ut (Faktiske)

9. november 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

9. november 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

3. november 2026

Sist bekreftet

1. november 2026

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

UBESLUTTE

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Ja

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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