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

3 de novembro de 2026 atualizado por: 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

Visão geral do estudo

Status

Ativo, não recrutando

Condições

Intervenção / Tratamento

Tipo de estudo

Intervencional

Inscrição (Estimado)

18

Estágio

  • Fase 1

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Locais de estudo

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

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

18 anos e mais velhos (Adulto, Adulto mais velho)

Aceita Voluntários Saudáveis

Sim

Gêneros Elegíveis para o Estudo

Tudo

Descrição

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.

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição cruzada
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: T1-T2-R group

Test drug T1

Reference drug

Test drug T2

Experimental: R-T1-T2 group

Test drug T1

Reference drug

Test drug T2

Experimental: T2-R-T1 group

Test drug T1

Reference drug

Test drug T2

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Cmax
Prazo: up to 48 hours post-dose

Primary PK parameters

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

Primary PK parameters

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

Primary PK parameters

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

Primary PK parameters

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

Secondary PK parameters

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

Secondary PK parameters

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

Secondary PK parameters

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

Secondary PK parameters

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

Secondary PK parameters

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

Secondary PK parameters

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

Secondary PK parameters

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

Secondary PK parameters

up to 48 hours post-dose

Medidas de resultados secundários

Medida de resultado
Prazo
Incidence of adverse events (AEs)
Prazo: Through study completion, an average of 13 days
Through study completion, an average of 13 days

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Patrocinador

Colaboradores

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

3 de novembro de 2026

Conclusão Primária (Estimado)

1 de janeiro de 2027

Conclusão do estudo (Estimado)

1 de janeiro de 2027

Datas de inscrição no estudo

Enviado pela primeira vez

3 de novembro de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

3 de novembro de 2026

Primeira postagem (Real)

9 de novembro de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

9 de novembro de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

3 de novembro de 2026

Última verificação

1 de novembro de 2026

Mais Informações

Termos relacionados a este estudo

Palavras-chave

Outros números de identificação do estudo

  • 2026-CP-D23A-01

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

INDECISO

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Sim

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

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