NCT07239973Befejeződött1. fázis
A Study of BGM0504 Tablets in Healthy and Non-diabetic Overweight or Obese Chinese Subjects
A Phase 1, Randomized, Double-Blind, Placebo-Controlled, Single/Multiple-dose Study to Evaluate the Safety, Pharmacokinetics and Pharmacodynamics of BGM0504 Tablets Orally Administered in Healthy and Non-diabetic Overweight or Obese Chinese Subjects.
Forrás: ClinicalTrials.gov · Utoljára frissítve: 2026. okt. 13.
Rövid összefoglaló (regiszter, angolul)
A Randomized, Double-Blind, Placebo-Controlled, Single/Multiple-dose Study to Evaluate the Safety, Pharmacokinetics and Pharmacodynamics of BGM0504 Tablets Orally Administered in Healthy and Non-diabetic Overweight or Obese Chinese Subjects.
- Állapot (regiszter)
- Befejeződött
- Fázis (regiszter)
- 1. fázis
- Vizsgálattípus
- Beavatkozással járó
- Résztvevők száma
- 75 (tényleges)
- Első benyújtás
- 2025. nov. 13.
- Kezdés
- 2025. okt. 24.
- Elsődleges befejezés
- 2026. márc. 5.
- Fő szponzor
- BrightGene Bio-Medical Technology Co., Ltd.
- Betegségek
- Elhízás
- NCT-szám
- NCT07239973
Mit vállalsz
- Vizsgálat típusa: Beavatkozással járó · 1. fázis
- Bevont résztvevők: 75
- 2025. okt. 24. és az elsődleges befejezés (2026. márc. 5.) között
- 1 helyszín, 1 országban
- Vizitek és vizsgálatok: kérdezd a vizsgálat csapatát, a regiszter nem sorolja fel őket
A(z) ClinicalTrials.gov regisztermezőiből összeállítva. A vizsgálat felépítését írja le.
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Korábbi kezelés
- Used illegal drugs within 6 months prior to screening, or substance abuse within 12 months prior to screening.
- Participated in drug or medical device clinical trials and treated with Study Drug (excluding placebo) or medical device intervention within 12 weeks before screening.
- Participants who have received any vaccine within 2 weeks prior to screening, or plan to receive a vaccine during the trial.
Más betegség
- Those with a history of severe drug allergies (especially those with known or suspected allergies to the active ingredients and excipients of BGM0504 Tablets), or complicated with severe specific allergic diseases/history, or with a severe allergic constitution.
- Subjects with positive results for HBsAg, anti-HCV, anti-HIV or anti-TP during the screening period.
- Has any other conditions or disorders deemed unsuitable for including in the study, in the opinion of the Investigator.
Laborértékek
- At the screening/baseline period, any one of the laboratory test indicators meets the following criteria:
- fasting serum glucose≥ 7.0mmol/L, or post-prandial glucose (PPG)-2h≥ 11.1mmol/L in oral glucose tolerance test (OGTT); (During screening, participants with fasting serum glucose ranging from 6.1 to 6.9mmol/L shall undergo the OGTT.)
- ALT, AST ≥ 2.5 times upper limit of normal (ULN) or total bilirubin ≥ 1.5 times upper limit of normal (ULN)
- Glomerular filtration rate (eGFR) ≤ 80 mL/min/1.73 m2(using CKD-EPI formula) or positive urine protein 2+ or more.
- Serum calcitonin level ≥ 35 ng/L (pg/mL);
- Thyroid-stimulating hormone (TSH) > 6.0mIU/L or < 0.4mIU/L;
- Fasting triglycerides ≥ 5.64mmol/L (500 mg/dL);
- Hemoglobin (Hgb) < 100 g/L (for females) or < 110 g/L (for males);
- 12-lead ECG shows ventricular heart rate < 50 beats/min or > 100 beats/min at screening/baseline, second or third degree atrioventricular block, long QT syndrome, QTcF> 470ms for women or > 450ms for men, pre-excitation syndrome or other significant arrhythmias.
- Positive urine drug test or alcohol serum test result at screening or at baseline.
Egyéb
- Female participants who are pregnant or lactating, or those with a positive pregnancy test result during the screening period.
Kiket keres a vizsgálat
- Between the ages of 18 and 65 years (inclusive) at the time of screening , healthy and non-diabetic overweight or obese subjects , both male and female;
- Healthy subjects , male weight ≥ 50 kg, female weight ≥ 45 kg, and body mass index (BMI): 20.0 kg/m² ≤ BMI < 28 kg/m²(BMI = weight/height²);
- Obese individuals: BMI ≥ 28.0 kg/m², or overweight individuals: 24.0 kg/m² ≤ BMI < 28.0 kg/m²;
- (Medical Inquiry) Have a stable body weight (<5% self-reported change during the previous 12 weeks) before screening.
- Have no history of mental disorders, be able to communicate smoothly with Investigator, Capable of understanding the written informed consent document; willingly provides valid, signed written informed consent; willing and able to comply with the schedule, requirements and restrictions of the study.
- Male subjects with female partners of reproductive potential must agree to practice abstinence or to use a condom (male subject) plus an additional medically acceptable form of contraception (female partner) for the duration of the study and for at least 3 months after dosing; must also agree to refrain from sperm donation for at least 3 months post dose
Életkor a regiszterben: 18 év – 55 év · Nem: nők és férfiak · Egészséges önkénteseket is fogad
Helyszínek (1)
Helyszínek a regiszter sorrendjében. Ha a profilodba mented a városodat, távolság szerint rendeződnek.
| Helyszín | Város | Ország | Helyszín állapota |
|---|---|---|---|
| The First Affiliated Hospital of Yunnan University of Chinese Medicine | Kunming | Kína | Ismeretlen állapot |
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