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Bioequivalence Study of Tenofovir Disoproxil Fumarate Tablets in Healthy Chinese Subjects

26 avril 2026 mis à jour par: Haisco Pharmaceutical Group Co., Ltd.

Bioequivalence and Safety Study of Tenofovir Disoproxil Fumarate Tablets in Healthy Chinese Subjects Under Fasting and Fed Conditions: a Randomized, Open-label, Single-dose, Crossover Study

This study evaluated the bioequivalence and safety of the test formulation (Tenofovir Disoproxil Fumarate Tablets, Haisco Pharmaceutical Group Co., Ltd.) and the reference formulation (Viread®, Gilead Sciences, Inc.) in healthy Chinese subjects under fasting and fed conditions

Aperçu de l'étude

Type d'étude

Interventionnel

Inscription (Réel)

47

Phase

  • La phase 1

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

      • Shenyang, Chine
        • General Hospital of Shenyang Military Region

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Adulte
  • Adulte plus âgé

Accepte les volontaires sains

Oui

La description

Inclusion Criteria:

  1. Healthy male and female subjects aged 18 years or older (including boundary values);
  2. Male weight ≥ 50 kg, female weight ≥ 45 kg, and body mass index (BMI) within the range of 19-26 kg/m² (including boundary values), where BMI = weight (kg) / height² (m²);
  3. Determined to be healthy based on medical history, physical examination, vital signs, and laboratory tests including blood routine, urinalysis, liver and kidney function, blood glucose, and electrocardiogram (ECG) during the screening period. All test results must be within the normal range consistent with age and sex, or meet the protocol requirements, or if outside the normal range, be judged by the investigator as having "no clinical significance (NCS)";
  4. No recent plans for pregnancy and agreement to use effective non-pharmacological contraceptive measures during the study period and within one month after study completion; Subjects able to communicate well with the investigator, understand and comply with all requirements of this study, and provide written informed consent.

Exclusion Criteria:

  1. A history of significant drug or food allergies judged by the investigator to be clinically meaningful, or known allergy to the study drug/class of drugs;
  2. Regular use of sedatives, hypnotics, or other addictive drugs, or a positive urine drug screen prior to dosing;
  3. A history of drug abuse, heavy smoking, or alcohol abuse within 12 months prior to dosing;
  4. Use of any prescription drugs or Chinese herbal supplements within 4 weeks prior to the first dose of the study drug, and/or use of any over-the-counter (OTC) medications or dietary supplements (including vitamins) within 2 weeks prior to the first dose of the study drug;
  5. Blood donation or participation in another clinical trial within 3 months prior to enrollment;
  6. A recent history (within the past 3 years) of autonomic nerve dysfunction and/or current medical history (e.g., recurrent syncope, palpitations, etc.);
  7. A past medical history of cardiovascular, hepatic, renal, pulmonary, gastrointestinal, or neurological diseases, any condition or illness that may significantly affect drug absorption, distribution, metabolism, or excretion, or any condition or illness that may pose a hazard to the subject participating in the trial. The investigator should consider the following medical history or conditions: history of inflammatory gastrointestinal disease, gastroesophageal reflux, gastrointestinal or rectal bleeding; history of pancreatic injury or pancreatitis; major surgical history such as gastrectomy, gastrointestinal anastomosis, or enterectomy. Clinically significant abnormalities in liver function laboratory tests, such as aspartate aminotransferase (AST), alanine aminotransferase (ALT), or bilirubin, indicating liver disease or liver injury, or exceeding 1.5 times the upper limit of normal;
  8. A history or evidence of acute or chronic renal insufficiency, such as serum creatinine above the upper limit of normal (still above the upper limit after repeated testing), clinically significant proteinuria, history of kidney transplantation, etc. A history of severe vomiting or diarrhea within one week prior to the trial;
  9. Subjects with an estimated endogenous creatinine clearance rate (calculated from serum creatinine levels during the screening period) below 80 mL/min (formula for endogenous creatinine clearance rate: Ccr = (140 - age) × body weight (kg) / [72 × Scr (mg/dL)] or Ccr = [(140 - age) × body weight (kg)] / [0.818 × Scr (μmol/L)]. Note the units of serum creatinine in the calculation; for female subjects, multiply the result by 0.85);
  10. Pregnant or lactating women, or women of childbearing age who cannot comply with the required contraceptive measures;
  11. Positive test for hepatitis B surface antigen (HBsAg), hepatitis C antibody (anti-HCV), syphilis, or HIV antibody;
  12. Subjects on a special diet, e.g., vegetarians;
  13. Subjects who refuse to abstain from any beverages or foods containing methylxanthines, such as caffeine (coffee, tea, cola, chocolate, etc.), from 48 hours before the start of the trial until the end of the trial;
  14. Subjects who refuse to abstain from any beverages or foods containing grapefruit from 7 days before the start of the trial until the end of the trial;
  15. Any other condition deemed by the investigator as unsuitable for enrollment.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Autre
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation croisée
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Test formulation (Test Tenofovir Disoproxil Fumarate Tablets)
Tenofovir Disoproxil Fumarate Tablets (300 mg/table) Manufacturer: Haisco Pharmaceutical Group Co., Ltd
Test formulation(Tenofovir Disoproxil Fumarate Tablets,Haisco Pharmaceutical Group Co., Ltd),A single oral dose of 300 mg, taken with 240mL of water
Expérimental: Reference formulation (Viread®)
Tenofovir Disoproxil Fumarate Tablets (Viread®,300 mg/table) Manufacturer: Gilead Sciences, Inc.
Reference formulation(Viread®,Gilead Sciences, Inc.)A single oral dose of 300 mg, taken with 240mL of water

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Cmax
Délai: From the start of administration to 72 hours post-dose
The maximum blood concentration, the pharmacokinetic parameters of tenofovir in plasma
From the start of administration to 72 hours post-dose
AUC(0-t) (Area Under the Concentration-Time Curve from time 0 to time t)
Délai: From the start of administration to 72 hours post-dose
The area under the blood concentration-time curve from time 0 to the last accurately measurable concentration at sample collection time t was measured, the pharmacokinetic parameters of tenofovir in plasma
From the start of administration to 72 hours post-dose
AUC(0-∞) (Area Under the Concentration-Time Curve from time 0 to infinity)
Délai: From the start of administration to 72 hours post-dose
The area under the blood concentration-time curve from 0 to infinite time (∞), the pharmacokinetic parameters of tenofovir in plasma
From the start of administration to 72 hours post-dose

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
AEs (Adverse events)
Délai: From the time of signing ICF (Informed Consent Form) to the end of follow-up,up to 10 days
The incidence and severity of adverse events
From the time of signing ICF (Informed Consent Form) to the end of follow-up,up to 10 days

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

20 juin 2017

Achèvement primaire (Réel)

23 août 2017

Achèvement de l'étude (Réel)

20 novembre 2017

Dates d'inscription aux études

Première soumission

19 avril 2026

Première soumission répondant aux critères de contrôle qualité

26 avril 2026

Première publication (Réel)

30 avril 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

30 avril 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

26 avril 2026

Dernière vérification

1 avril 2026

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • HSK-TDF-BE-1.0-161030

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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