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क्लिनिकल ट्रायल NCT07295873 के लिए Chronic Hepatitis B Liver Fibrosis, DDI (Drug-Drug Interaction) वर्तमान में अभी भर्ती शुरू नहीं है। सभी विवरणों के लिए क्लिनिकल ट्रायल रडार कार्ड दृश्य और AI खोज उपकरण देखें, या यहाँ कुछ भी पूछें।
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Drug-Drug Interaction Study Between Hydronidone and Entecavir, Tenofovir Disoproxil Fumarate, Tenofovir Alafenamide, and Tenofovir Amibufenamide चरण I 64

अभी भर्ती शुरू नहीं
चिकित्सा परीक्षण का विवरण मुख्य रूप से अंग्रेजी में उपलब्ध है। हालाँकि, ट्रायल रडार AI मदद कर सकता है! बस 'अध्ययन समझाएं' पर क्लिक करें और अपनी चुनी हुई भाषा में परीक्षण की जानकारी देखें और चर्चा करें।
क्लिनिकल ट्रायल NCT07295873 का मुख्य उद्देश्य उपचार का अध्ययन करना है। यह चिकित्सकीय अध्ययन Chronic Hepatitis B Liver Fibrosis, DDI (Drug-Drug Interaction) से जुड़ा हुआ है और यह एक चरण I हस्तक्रियात्मक परीक्षण है। परीक्षण वर्तमान में अभी भर्ती शुरू नहीं चल रहा है। इसमें 64 प्रतिभागियों को शामिल करने की योजना है और प्रतिभागियों का नामांकन 30 दिसंबर 2025 से शुरू होगा। गायर थेरेप्यूटिक्स इस परीक्षण का नेतृत्व कर रहे हैं और इसके 30 जून 2026 तक पूरा होने की उम्मीद है। ClinicalTrials.gov वेबसाइट पर यह जानकारी 22 दिसंबर 2025 को अंतिम बार अपडेट की गई थी।
संक्षिप्त सारांश
The proposed indication for Hydronidone Capsules is chronic hepatitis B-associated liver fibrosis, which in clinical practice typically requires concomitant use with antiviral agents for chronic hepatitis B. The commonly used chronic hepatitis B antiviral agents include Entecavir, Tenofovir Disoproxil Fumarate (TDF), Tenofovir Alafenamide (TAF), and Tenofovir Amibufenamide (TMF).

This study aims to evaluate the drug...

और दिखाएँ
आधिकारिक शीर्षक

A Single-Center, Open-Label, Single-Arm, Self-Controlled Phase I Clinical Study to Evaluate Drug-Drug Interactions of Hydronidone With Entecavir, Tenofovir Disoproxil Fumarate, Tenofovir Alafenamide, and Tenofovir Amibufenamide in Healthy Chinese Subjects

स्वास्थ्य स्थितियां
Chronic Hepatitis B Liver FibrosisDDI (Drug-Drug Interaction)
अन्य अध्ययन आईडी
  • KDN-F351-202505
NCT नंबर
NCT07295873
अध्ययन प्रारंभ तिथि (वास्तविक)
2025-12-30
अंतिम अद्यतन प्रकाशित
2025-12-22
अध्ययन की समाप्ति तिथि (अनुमानित)
2026-06-30
नामांकन (अनुमानित)
64
अध्ययन प्रकार
हस्तक्रियात्मक
चरण
चरण I
स्थिति
अभी भर्ती शुरू नहीं
प्रमुख शब्द
Hydronidone
F351
प्राथमिक उद्देश्य
उपचार
डिज़ाइन आवंटन
गैर-यादृच्छिक
हस्तक्षेप मॉडल
एकल समूह
अंधकरण
कोई नहीं (खुला लेबल)
समूह/हस्तक्षेप
प्रतिभागी समूह/शाखाहस्तक्षेप/उपचार
प्रयोगात्मकQueue 1: Drug-Drug Interaction Study of Hydronidone Capsules and Entecavir
Within each cohort, the study flow for enrolled subjects comprises three dosing periods: Period 1 consists of hydronidone capsules administered alone for 5 consecutive days; Period 2 consists of the chronic hepatitis B antiviral agent administered alone for 7 or 10 consecutive days; and Period 3 consists of concomitant administration of hydronidone capsules and the antiviral agent for 5 consecutive days. Subjects may...और दिखाएँ
Entecavir
0.5 mg, taken orally on an empty stomach, once a day
प्रयोगात्मकQueue 2: Drug-Drug Interaction Study of honyinone capsules and Tenofovir Disoproxil Fumarate;
Within each cohort, the study flow for enrolled subjects comprises three dosing periods: Period 1 consists of hydronidone capsules administered alone for 5 consecutive days; Period 2 consists of the chronic hepatitis B antiviral agent administered alone for 7 or 10 consecutive days; and Period 3 consists of concomitant administration of hydronidone capsules and the antiviral agent for 5 consecutive days. Subjects may...और दिखाएँ
Tenofovir Disoproxil Fumarate（TDF）
300 mg, taken orally on an empty stomach, once a day
प्रयोगात्मकDrug-Drug Interaction Study of Fuzuloprim Capsules with Tenofovir Alafenamide
Within each cohort, the study flow for enrolled subjects comprises three dosing periods: Period 1 consists of hydronidone capsules administered alone for 5 consecutive days; Period 2 consists of the chronic hepatitis B antiviral agent administered alone for 7 or 10 consecutive days; and Period 3 consists of concomitant administration of hydronidone capsules and the antiviral agent for 5 consecutive days. Subjects may...और दिखाएँ
Tenofovir alafenamide（TAF）
25 mg, single oral dose, under fasting conditions
प्रयोगात्मकQueue 4: Drug-Drug Interaction Study of Hydronidone Capsules and Tenofovir Amibufenamide
Within each cohort, the study flow for enrolled subjects comprises three dosing periods: Period 1 consists of hydronidone capsules administered alone for 5 consecutive days; Period 2 consists of the chronic hepatitis B antiviral agent administered alone for 7 or 10 consecutive days; and Period 3 consists of concomitant administration of hydronidone capsules and the antiviral agent for 5 consecutive days. Subjects may...और दिखाएँ
Tenofovir Amibufenamide(TMF)
25 mg, single oral dose, under fasting conditions
प्राथमिक परिणाम माप
परिणाम मापमाप विवरणसमय सीमा
Plasma hydronidone PK parameters of hydronidone capsules : steady-state peak concentration (Cmax,ss);
23 days
Plasma hydronidone PK parametersof hydronidone capsules : Area under the plasma concentration-time curve from time zero to 24 hours at steady state (AUC0-24h,ss)
23 days
Primary PK parameters of plasma of entecavir : AUC0-24h,ss.
23 days
Primary PK parameters of plasma of entecavir : Cmax,ss .
23 days
Primary PK parameters of plasma tenofovir alafenamide (TAF) : AUC0-24h,ss.
23 days
Primary PK parameters of plasma tenofovir alafenamide (TAF) : Cmax,ss .
23 days
Primary PK parameters of tenofovir disoproxil fumarate tablets (TDF): Cmax,ss .
20 days
Primary PK parameters of tenofovir disoproxil fumarate tablets (TDF): AUC0-24h,ss.
20 days
Primary PK parameters of plasma tenofovir amibufenamide (TMF) : Cmax,ss .
23 days
Primary PK parameters of plasma tenofovir amibufenamide (TMF) : AUC0-24h,ss.
23 days
भागीदारी सहायक
पात्रता मानदंड

अध्ययन के लिए पात्र आयु
वयस्क
अध्ययन के लिए न्यूनतम आयु
18 Years
अध्ययन के लिए पात्र लिंग
सभी
स्वस्थ स्वयंसेवकों को स्वीकार करता है
हाँ
  • Be fully informed about the trial and demonstrate understanding of its content, procedures, and potential adverse events related to the investigational product; voluntarily provide written informed consent; and be able to comply with all study procedures and complete the study in accordance with the protocol requirements.
  • Male or female subjects aged 18 to 50 years, inclusive, at the time of signing informed consent.
  • At screening, male subjects must weigh ≥50.0 kg and female subjects must weigh ≥45.0 kg, with a body mass index (BMI) between 19.0 and 26.0 kg/m², inclusive.
  • At screening, all laboratory tests and related examinations (including vital signs, physical examination, 12-lead ECG, chest X-ray \[PA view\], abdominal ultrasound, etc.) must be within normal range or, if abnormal, determined by the investigator to be not clinically significant.

  • Presence of any clinically significant disease or medical history that, in the opinion of the investigator, may interfere with protocol compliance or completion of the study, including but not limited to abnormalities of the central nervous system, cardiovascular system, digestive system, respiratory system, urinary system, hematologic system, immune system, psychiatric system, or endocrine/metabolic system.
  • Positive results for any infectious disease screening tests at screening, including hepatitis B surface antigen (HBsAg), hepatitis C antibody (HCV Ab), human immunodeficiency virus antigen/antibody (HIV Ag/Ab), or Treponema pallidum antibody (TP Ab).
  • History of drug or food allergies, or known hypersensitivity to the active pharmaceutical ingredients of the investigational medicinal products (hydronidone, entecavir, tenofovir disoproxil fumarate, tenofovir alafenamide, tenofovir amibufenamide) or to any of their excipients.
  • Participants with rare genetic disorders of galactose intolerance, lactase deficiency, or glucose-galactose malabsorption;
  • Subjects who have experienced a clinically significant major illness within 3 months prior to screening, or have undergone surgery affecting drug absorption, distribution, metabolism, or excretion (such as gastrointestinal, hepatic, or renal surgery) or other major surgery within this period, or plan to undergo surgery during the study;
  • Subjects who have donated blood or experienced blood loss ≥400 mL within 3 months prior to dosing, or received blood transfusion or blood products within 4 weeks prior to dosing, or plan to donate blood during the study period;
  • Subjects who have participated as a participant in any clinical trial and received investigational drug or device treatment within 3 months prior to dosing;
  • Subjects who have taken any prescription medication, over-the-counter medication, vitamin products, or herbal medicines within 14 days or 5 half-lives (if known) prior to dosing, whichever is longer; or who have taken strong inhibitors or inducers of CYP3A4, P-glycoprotein (P-gp), breast cancer resistance protein (BCRP), OATP1B1, OATP1B3, or OAT1/3 within 4 weeks prior to screening; or any drugs known to cause QT/QTc interval prolongation or with a known risk of causing torsades de pointes (TdP) (see Appendix 2); or plan to use any chemical drugs, biological products, traditional Chinese medicines, or natural medicines that the investigator deems inappropriate during the trial period;
  • Subjects who received vaccination within 4 weeks prior to screening, or plan to receive vaccination during the study period up to 1 month after the last dose; Subjects with a history of drug abuse within the past 5 years, or who used illicit drugs within 3 months prior to screening, or with a positive urine drug abuse screen at baseline;
  • Subjects who regularly consumed alcohol within 6 months prior to dosing, i.e., more than 14 units of alcohol per week (1 unit = 360 mL of beer or 45 mL of 40% alcohol spirits or 150 mL of wine), or who refuse to abstain from alcohol or alcohol-containing products during the trial, or with a positive alcohol breath test at baseline;
  • Subjects who smoked more than 5 cigarettes daily within 3 months prior to dosing, or who are unable to discontinue use of tobacco products during the trial period;
  • Subjects with a history of blood-needle phobia/syncope, or unable to tolerate venous indwelling needle puncture;
  • Subjects with special dietary requirements who cannot follow the standardized diet, or with difficulty swallowing;
  • Subjects unable to avoid specific foods/diet during the trial period, including dragon fruit, mango, grapefruit or grapefruit-related citrus fruits (e.g., Seville orange, pomelo), star fruit, papaya, pomegranate or products thereof, and/or xanthine-containing diet, caffeine-containing food or beverages, strong tea, etc.;
  • Subjects who consumed grapefruit or grapefruit-related citrus fruits (e.g., Seville orange, pomelo) or products thereof within 2 weeks prior to dosing, or who consumed specific diet (including dragon fruit, mango and/or xanthine-containing diet, caffeine-containing food or beverages, strong tea, etc.) within 48 hours prior to dosing, or engaged in strenuous exercise, or have other factors that may affect drug absorption, distribution, metabolism, or excretion;
  • Pregnant or lactating women, or female subjects of childbearing potential with a positive serum pregnancy test at screening;
  • Subjects of childbearing potential who do not agree to use effective contraceptive methods from the time of signing informed consent until 3 months after study completion (see Appendix 3), or do not agree to avoid freezing or donating eggs or sperm during this period;
  • Subjects who, in the opinion of the investigator, have other reasons that render them unsuitable for participation in this study.
Beijing Continent Pharmaceutical Co, Ltd. logoगायर थेरेप्यूटिक्स
अध्ययन केंद्रीय संपर्क
संपर्क: Ling Zhang, 010-88877935-801, [email protected]
1 1 देशों में अध्ययन स्थान
Beijing Gaobo Hospital, Beijing, 100000, China
Quankun / Xumei Zhuang / Liu, संपर्क, 13011825339, [email protected]