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Clinical Trials of IBI3035 in Healthy Subjects

14. juli 2026 oppdatert av: Innovent Biologics (Suzhou) Co. Ltd.

Evaluation of the Pharmacokinetics and Pharmacodynamics of IBI3035 and Awiqli? (Ecoporin Insulin Injection) in a Randomized, Open-label, Single-dose, Two-formulation, Crossover Design in Healthy Male Subjects in China: A Phase I Clinical Trial.

This study is a Phase I clinical trial that uses positive glucose clamping technology to evaluate the pharmacokinetic (PK) and pharmacodynamic (PD) bioequivalence of IBI3035 with insulin injection (Awiqli?) after a single administration in healthy male subjects

Studieoversikt

Status

Rekruttering

Forhold

Studietype

Intervensjonell

Registrering (Antatt)

144

Fase

  • Fase 1

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Studiesteder

    • Chongqing Municipality
      • Chongqing, Chongqing Municipality, Kina, 402760
        • Rekruttering
        • Bishan Hospital of Chongqing
        • Ta kontakt med:

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Voksen

Tar imot friske frivillige

Ja

Beskrivelse

Inclusion Criteria

The following inclusion criteria must be met:

  1. Healthy male adult subjects aged 18 to 45 years (including 18 and 45 years, based on the date of signing the informed consent form) of Chinese nationality;
  2. Body Mass Index (BMI) between 19.0 and 24.0 kg/m2 (including both values) at screening, and weight ≥ 50 kg;
  3. Normal glucose tolerance at screening [3.9 mmol/L < fasting blood glucose < 6.1 mmol/L, and 2-hour post-glucose load blood glucose < 7.8 mmol/L in the oral glucose tolerance test (OGTT)]; normal insulin secretion function or abnormality without clinical significance as determined by the investigator [confirmed by the insulin release test (IRT)];
  4. Glycated hemoglobin ≤ 6.0% at screening;
  5. Agree to take effective contraceptive measures during the study period and within 6 months after the last dose and have no plan to donate sperm;
  6. Able to understand the procedures and methods of this study, willing to strictly follow the clinical trial protocol to complete the trial, and voluntarily sign the informed consent form.

Exclusion Criteria

Subjects who meet any of the following exclusion criteria cannot be included in this study:

  1. Known or suspected to be allergic to the investigational drug in this study;
  2. Have taken any drugs that affect insulin hypoglycemic effects within 28 days before screening (such as corticosteroids, diuretics, epinephrine, salbutamol, glucagon, thyroid hormones, etc.);
  3. Have a history of clinical significance as determined by the investigator at screening or before randomization, including diseases of the endocrine system, blood system, cardiovascular system, respiratory system, digestive system, urinary system, immune system, nervous system, or any other disease that can significantly alter the absorption, metabolism, or elimination of drugs;
  4. Have a clear diagnosis of hyperglycemia or hypoglycemia within 3 months before screening;
  5. Have an increased risk of thrombosis at screening, including personal or family history of deep vein thrombosis;
  6. Have abnormal indicators with clinical significance at screening or before randomization: vital signs, physical examination, laboratory tests, chest X-ray, and 12-lead ECG as determined by the investigator;
  7. Have had a severe infection, trauma, or surgery within 4 weeks before screening;
  8. Have smoked more than 5 cigarettes per day within 3 months before screening, or have smoked within 48 hours before using the investigational drug or cannot stop using any tobacco products during the trial;
  9. Have used any prescription drugs, Chinese herbal medicines, over-the-counter drugs, or health supplements (except for regular vitamin supplements) within 2 weeks before screening;
  10. Have donated blood ≥ 400 ml or had any component blood donation within 3 months before screening, or have lost a total of ≥ 400 ml of blood for any reason, or have a history of blood transfusion or use of blood products;
  11. Have consumed more than 14 units of alcohol per week within 3 months before screening: 1 unit ≈ 360 ml of beer, or 45 ml of spirits, or 150 ml of wine, and cannot abstain from alcohol within 48 hours before using the investigational drug;
  12. Have consumed excessive amounts of tea, coffee, and/or caffeine-rich beverages (more than 8 cups, 1 cup ≈ 250 ml) daily within 3 months before screening;
  13. Have positive results for human immunodeficiency virus (HIV) antibodies, hepatitis B surface antigen (HBsAg), hepatitis C virus (HCV) antibodies, or Treponema pallidum antibodies;
  14. Have a history of drug abuse or drug use within 3 months before screening, or have positive results for alcohol tests or urine drug screening at screening. 15. Participants who have participated in other clinical trials and used investigational drugs or medical devices within the 3 months prior to screening;

16. Participants with a weight change greater than 5% within the 3 months prior to screening [(maximum weight within the 3 months prior to screening - minimum weight within the 3 months prior to screening) / minimum weight within the 3 months prior to screening × 100%, as self-reported by the participant]; 17. Participants with any food allergies or special dietary requirements that prevent them from adhering to a uniform diet (such as intolerance to standard meal foods, lactose intolerance, etc.); 18. Participants who have experienced acute diseases during the screening period; 19. Participants with a history of fainting at the sight of needles or blood, who cannot tolerate venipuncture blood collection, or who have difficulty with blood collection; 20. Participants for whom the investigator deems there to be any circumstances that make them unsuitable for participation in the trial.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Randomisert
  • Intervensjonsmodell: Crossover-oppdrag
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Aktiv komparator: Insulin icodec Injection
The first cycle is Awiqli® 1 U/kg, and the second cycle is IBI3035 1 U/kg
IBI3035 administered subcutaneously(SC)
Insulin icodec Injection administered subcutaneously(SC)
Eksperimentell: IBI3035
The first cycle is IBI3035 1 U/kg, and the second cycle is Awiqli® 1 U/kg
IBI3035 administered subcutaneously(SC)
Insulin icodec Injection administered subcutaneously(SC)

Hva måler studien?

Primære resultatmål

Resultatmål
Tidsramme
The area under the blood drug concentration-time curve from 0 to 168 hours
Tidsramme: From 0 to 168 hours after administration
From 0 to 168 hours after administration
Area Under Curve Glucose Infusion Rate (AUCGIR) 0-168h
Tidsramme: From 0 to 168 hours after administration
From 0 to 168 hours after administration

Sekundære resultatmål

Resultatmål
Tidsramme
Area Under Curve (AUC0-84h)
Tidsramme: From 0 to 84 hours after administration
From 0 to 84 hours after administration
Tmax
Tidsramme: From 0 to 168 hours after administration
From 0 to 168 hours after administration
Glucose Infusion Rate (GIR) max
Tidsramme: From 0 to 168 hours after administration
From 0 to 168 hours after administration
Area Under Curve Glucose Infusion Rate (AUCGIR) 24-48h
Tidsramme: From 24 to 48 hours after administration
From 24 to 48 hours after administration
Adverse events (AE)
Tidsramme: through study completion, an average of 16 weeks
through study completion, an average of 16 weeks
The generation of Anti-drug antibodies (ADA) and Neutrolizing antibodies (NAb if required)
Tidsramme: through study completion, an average of 16 weeks
through study completion, an average of 16 weeks
Area Under Curve (AUC) 84-168h
Tidsramme: From 84 to 168 hours after administration
From 84 to 168 hours after administration
Cmax
Tidsramme: From 0 to 168 hours after administration
From 0 to 168 hours after administration
T1/2
Tidsramme: From 0 to 168 hours after administration
From 0 to 168 hours after administration
tGIRmax
Tidsramme: From 0 to 168 hours after administration
From 0 to 168 hours after administration
AUCGIR 144-168h
Tidsramme: From 144 to 168 hours after administration
From 144 to 168 hours after administration
vital signs (Body temperature)
Tidsramme: through study completion, an average of 16 weeks
through study completion, an average of 16 weeks
laboratory tests (fasting plasma glucose (GLU))
Tidsramme: through study completion, an average of 16 weeks
through study completion, an average of 16 weeks
12-lead Electrocardiogram (RR interval, PR interval, heart rate (HR), QRS interval, QT interval, QTcF (QTcF = QT/RR^0.33))
Tidsramme: through study completion, an average of 16 weeks
through study completion, an average of 16 weeks
vital signs (pulse)
Tidsramme: through study completion, an average of 16 weeks
through study completion, an average of 16 weeks
vital signs (respiratory rate)
Tidsramme: through study completion, an average of 16 weeks
through study completion, an average of 16 weeks
vital signs (blood pressure: systolic, diastolic)
Tidsramme: through study completion, an average of 16 weeks
through study completion, an average of 16 weeks

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

8. mai 2026

Primær fullføring (Antatt)

30. juli 2027

Studiet fullført (Antatt)

31. august 2027

Datoer for studieregistrering

Først innsendt

21. april 2026

Først innsendt som oppfylte QC-kriteriene

11. mai 2026

Først lagt ut (Faktiske)

15. mai 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

16. juli 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

14. juli 2026

Sist bekreftet

1. juli 2026

Mer informasjon

Begreper knyttet til denne studien

Ytterligere relevante MeSH-vilkår

Andre studie-ID-numre

  • CIBI3035A101CN
  • MR-50-26-033399 (Annen identifikator: Medical Research Registration Information System)

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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