Denna sida har översatts automatiskt och översättningens korrekthet kan inte garanteras. Vänligen se engelsk version för en källtext.

A Phase 1, Multiple Ascending Dose Study to Evaluate HMS1005 in Participants With Type 2 Diabetes

28 april 2026 uppdaterad av: Hua Medicine Limited

A Phase 1, Randomized, Placebo-Controlled, Double-Blind, Multiple- Dose Escalation Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of HMS1005 in Participants With Type 2 Diabetes

The study is to assess the safety, pharmacokinetics, and pharmacodynamic profile of HMS1005 in patient with diabetes

Studieöversikt

Status

Rekrytering

Betingelser

Studietyp

Interventionell

Inskrivning (Beräknad)

40

Fas

  • Fas 1

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studiekontakt

Studieorter

    • Florida
      • Miami, Florida, Förenta staterna, 33172
        • Rekrytering
        • Clinical Pharmacology of Miami
        • Kontakt:
        • Huvudutredare:
          • Alexander N Prezioso, MD

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

  • Vuxen
  • Äldre vuxen

Tar emot friska volontärer

Nej

Beskrivning

Inclusion Criteria:

  1. Males or females, of any race, between 18 and 65 years of age, inclusive.
  2. Body mass index between 18 and 38.0 kg/m2, inclusive.
  3. Females will not be pregnant or lactating, and females of childbearing potential and males will agree to use contraception as detailed in Appendix 3.
  4. T2DM, as determined by the ADA Standard Care Diagnostic Criteria 2025, and

    • are drug naïve, treated with diet and exercise, or
    • have been on a stable dose of ≤2000 mg metformin for ≥1 month, and/or
    • have been on a stable dose of other antidiabetic medications for ≥90 days.
  5. Except for findings consistent with T2DM, in good health, determined from medical history, 12-lead electrocardiogram (ECG), vital signs measurements, clinical laboratory evaluations, and physical examinations at screening and/or check in, as assessed by the Investigator (or designee).
  6. Doses of antihypertensive and lipid-lowering therapies must be stable for 30 days prior to screening and remain unchanged during the study unless necessary to protect participant safety on an emergency basis (e.g., hypertensive crisis).
  7. Glycated hemoglobin between 7.0% and 10.5%, inclusive.
  8. Fasting plasma glucose between 126 and 240 mg/dL, inclusive. Testing may be repeated once, at the discretion of the Investigator (or designee).
  9. Able to comprehend and willing to sign an ICF and to abide by the study restrictions.

Exclusion Criteria:

  1. Type 1 diabetes mellitus, maturity onset diabetes of the young, or diabetes mellitus caused by damage to the pancreas or any other condition (eg, acromegaly or Cushing's syndrome).
  2. Diabetic neuropathy, retinopathy, or nephropathy.
  3. History of acute diabetic complications such as diabetic ketoacidosis, hyperglycemic hyperosmolar syndrome, lactic acidosis, or hyperosmolar nonketotic coma within the 6 months prior to screening, or chronic metabolic acidosis.
  4. History of severe hypoglycemia, defined as severe cognitive impairment requiring external assistance for recovery within 3 months prior to dosing; or recurrent hypoglycemia (Level 2), defined as ≥2 episodes within 3 months prior to dosing; or ADA Level 3 hypoglycemia within 6 months prior to dosing.
  5. Hypoglycemia unawareness or asymptomatic hypoglycemia.
  6. Clinically significant history of liver disease (eg, hepatitis and cirrhosis) within 1 year prior to screening.
  7. Clinically significant history of renal disease. Mild to moderate chronic kidney disease is permitted.
  8. Clinically significant history of cardiovascular disease, particularly coronary artery disease, arrhythmias, atrial tachycardia, or congestive heart disease within 1 year prior to screening. Managed hypertension is permitted (defined as systolic blood pressure <160 mmHg and/or diastolic blood pressure <100 mmHg).
  9. Clinically significant history of any central nervous system or psychiatric disease, including transient ischemic attack, stroke, seizure disorder, depression, or behavioral disturbances within 1 year prior to screening.
  10. Clinically significant gastric emptying abnormality (eg, severe diabetic gastroparesis or gastric outlet obstruction) or have had gastric bypass surgery.
  11. Clinically significant or unstable history of any hepatic, renal, hematological, pulmonary, cardiovascular, gastrointestinal, neurological, endocrine, or psychiatric disorder, as determined by the Investigator (or designee).
  12. Known or active malignancy, except basal cell carcinoma and cutaneous squamous cell carcinoma.
  13. Any hospital admission or major surgery within 90 days prior to screening.
  14. History of significant hypersensitivity, intolerance, or allergy to any drug compound, food, or other substance, as determined by the Investigator (or designee).
  15. Fasting C peptide < 0.81 ng/mL.
  16. Alanine aminotransferase, aspartate aminotransferase, or gamma glutamyl transferase >2 × the upper limit of normal (ULN); or total bilirubin >1.5× ULN. Testing may be repeated once, at the discretion of the Investigator (or designee).
  17. Uncontrolled hypertriglyceridemia > 500 mg/dL.
  18. Estimated glomerular filtration rate ≤ 45 mL/minutes/1.73 m2, as calculated using the 2021 Chronic Kidney Disease Epidemiology equation.
  19. Hemoglobin ≤120 g/L (male) or ≤110 g/L (female).
  20. QT interval corrected for heart rate using Fridericia's method > 450 msec.
  21. Positive hepatitis B surface antigen, hepatitis C antibody, human immunodeficiency (HIV 1 and HIV 2) antibodies and p24 antigen.
  22. Positive pregnancy test.
  23. Use of insulin, sulfonylureas, GLP-1 agonists, DPP-4 inhibitors, SGLT2 inhibitor and glinides (eg, repaglinide and nateglinide).
  24. Use of any strong or moderate cytochrome P450 (CYP) 3A4 inducers within 28 days prior to dosing or any strong or moderate CYP3A4 inhibitors within 7 days or 5 half-lives, whichever is longer, prior to dosing (Appendix 5).
  25. Use of any P glycoprotein inducers within 14 days prior to dosing or any P glycoprotein inhibitors within 5 days or 5 half-lives, whichever is longer, prior to dosing (Appendix 6).
  26. Use of any carboxylesterase 2 inhibitors within 5 days or 5 half-lives, whichever is longer, prior to dosing (Appendix 7).
  27. Participation in a clinical study involving administration of an investigational drug (new chemical entity) in the past 30 days.
  28. Positive alcohol test result, or positive urine drug screen (confirmed by repeat) at screening or check in.
  29. Current drug abuse, defined as the use of any illegal substance or misuse or excessive used of over the counter or prescription drugs; or current alcohol abuse, defined as the inability to stop or control alcohol use, despite adverse social or health consequences.
  30. Consumption of alcohol, or caffeine containing foods or beverages within 48 hours, or foods and beverages containing grapefruit or Seville oranges within 7 days prior to check in.
  31. Use of tobacco or nicotine containing products within 1 month prior to screening.
  32. Receipt or donation of > 1 unit (approximately 450 mL) of blood products within 3 months prior to screening.
  33. Poor peripheral venous access.
  34. Participants who, in the opinion of the Investigator (or designee), should not participate in this study.

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Behandling
  • Tilldelning: Randomiserad
  • Interventionsmodell: Sekventiell tilldelning
  • Maskning: Dubbel

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: 123 mg HMS1005 (1 x 123 mg tablet) and matching placebo
active vs placebo: 6 to 2
Matchande placebo
The investigational medicinal products (IMPs) HMS1005 ER tablets
Experimentell: 184.5 mg HMS1005 (1 x 184.5 mg tablet) and matching placebo
active vs placebo: 6 to 2
Matchande placebo
The investigational medicinal products (IMPs) HMS1005 ER tablets
Experimentell: 369 mg HMS1005 (2 x 184.5 mg tablet) and matching placebo
active vs placebo: 6 to 2
Matchande placebo
The investigational medicinal products (IMPs) HMS1005 ER tablets
Experimentell: 492 mg HMS1005 (2 x 246 mg tablet) and matching placebo
active vs placebo: 6 to 2
Matchande placebo
The investigational medicinal products (IMPs) HMS1005 ER tablets
Experimentell: 246 mg HMS1005 (1 x 246 mg tablet) or placebo
active vs placebo: 6 to 2
Matchande placebo
The investigational medicinal products (IMPs) HMS1005 ER tablets

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Incidence of adverse events
Tidsram: From enrollment to the end of treatment at Day 19
incidence and severity of adverse events from Day1 to Day 19
From enrollment to the end of treatment at Day 19
Area under the plasma concentration versus time curve (AUC)
Tidsram: Single-dose: Day 1-3 steady-state: Day 14-17
Measure area under the concentration-time curve from time 0 to 72 hours postdose of HM-002-1005 in plasma after single-dose and at steady-state
Single-dose: Day 1-3 steady-state: Day 14-17
Maximum observed concentration (Cmax)
Tidsram: Single-dose: Day 1-3 steady-state: Day 14-17
Cmax of HM-002-1005 in plasma after single and multiple dose
Single-dose: Day 1-3 steady-state: Day 14-17
Time of the maximum observed concentration (Tmax)
Tidsram: Single-dose: Day 1-3 steady-state: Day 14-17
Time of the maximum observed concentration (Tmax) of HM-002-1005
Single-dose: Day 1-3 steady-state: Day 14-17
Apparent terminal elimination half life (t1/2)
Tidsram: Single-dose: Day 1-3 steady-state: Day 14-17
t1/2 of HM-002-1005 in plasma
Single-dose: Day 1-3 steady-state: Day 14-17

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Glucose concentration
Tidsram: Day -1 and 14
Measure serum glucose concentration over 24 hours after dosing
Day -1 and 14
Glucose time in range (70-180 mg/dL) %
Tidsram: From Day -10 (baseline) to Day 17
Percentage of glucose time in range (70-180 mg/dL) will measured by continous glucose monitor
From Day -10 (baseline) to Day 17

Andra resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Insulin concentration
Tidsram: Day -2, -1, 13, and 14
Measure serum insulin concentration under fasting condition and postmeal
Day -2, -1, 13, and 14
C-peptide concentration
Tidsram: Day -2, -1, 13, and 14
C-peptide concentration under fasting and after meal
Day -2, -1, 13, and 14
Glucagon concentration
Tidsram: Day -2, -1, 13, and 14
Measure serum glucagon concentration under fasting and postmeal
Day -2, -1, 13, and 14
GLP-1 concentration
Tidsram: Day -1 and Day 14
Measure postmeal GLP-1 concentration in blood
Day -1 and Day 14

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Samarbetspartners

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Faktisk)

4 december 2025

Primärt slutförande (Beräknad)

13 augusti 2026

Avslutad studie (Beräknad)

13 oktober 2026

Studieregistreringsdatum

Först inskickad

20 januari 2026

Först inskickad som uppfyllde QC-kriterierna

28 april 2026

Första postat (Faktisk)

6 maj 2026

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

6 maj 2026

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

28 april 2026

Senast verifierad

1 april 2026

Mer information

Termer relaterade till denna studie

Plan för individuella deltagardata (IPD)

Planerar du att dela individuella deltagardata (IPD)?

NEJ

Läkemedels- och apparatinformation, studiedokument

Studerar en amerikansk FDA-reglerad läkemedelsprodukt

Ja

Studerar en amerikansk FDA-reglerad produktprodukt

Nej

Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .

Prenumerera