Denne siden ble automatisk oversatt og nøyaktigheten av oversettelsen er ikke garantert. Vennligst referer til engelsk versjon for en kildetekst.

Multiple Ascending Doses of SY-008 in Type 2 Diabetes Mellitus

A Phase Ib Placebo-controlled Study to Assess Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of SY-008 After Multiple Ascending Doses in Patients With Type 2 Diabetes Mellitus

This is a phase Ib placebo-controlled study to assess safety, tolerability, pharmacokinetics and pharmacodynamics of SY-008 after Multiple Ascending Doses in patients with Type 2 Diabetes Mellitus (T2DM).

Studieoversikt

Detaljert beskrivelse

This is a multicenter, randomized, double-blind, placebo-controlled, dose-increasing, multiple oral administration clinical trial. The planned dose increasing level was 6, 12 and 18 mg daily dose (3 administration groups).

After the completion of the test and safety evaluation of the initial dose 6mg daily dose group, the main researchers of the team leader and the sponsor jointly determine whether to enter the 12mg daily dose study.

After the completion of the test and safety evaluation of the 12 mg daily dose group, the main researchers of the team leader and the sponsor jointly determine whether to enter the 18 mg daily dose study.

Studietype

Intervensjonell

Registrering (Faktiske)

30

Fase

  • Fase 1

Kontakter og plasseringer

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

Studiesteder

    • Jiangsu
      • Nanjing, Jiangsu, Kina, 210093
        • Nanjing Gulou Hospital

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

18 år til 65 år (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

Inclusion Criteria:

  • body weight of male ≥ 50kg, female ≥ 45kg, and body mass index (BMI) between 18.0 and 35.0 kg / m2 (including the threshold value) at screening;
  • Have T2DM prior to entering the trial based on the disease diagnostic criteria (WHO, 1999), and currently being treated with diet and exercise only for at last 12 weeks , or no systemic treatment of diabetes (the cumulative use of antidiabetic drugs in the past 3 months has lasted no more than 2 weeks and no antidiabetic drugs has been used in the past month);
  • 7% ≤ HbA1c ≤ 9.5% at screening;
  • 7 mmol/L≤FPG ≤ 13.3 mmol/L at baseline;
  • During the study period and within 60 days after the end of the study, the subjects has no fertility or sperm / egg donation plan and will voluntarily take effective physical contraceptive measures;
  • Have given written informed consent to participate in this study, are well motivated, capable, and willing to communicate with the investigator and complete all the requirements according to the protocol.

Exclusion Criteria:

  • Those who are known to be allergic to the test drug (including the auxiliary materials of the test drug) or its analogues, or who are allergic to two or more drugs, food and pollen, or who have taken SGLT1 or SGLT2 inhibitors in the past year;
  • It was diagnosed as type 1 diabetes, or gestational diabetes, or other special type diabetes;
  • There is enough evidence to show that there is proliferative retinopathy of active diabetes;
  • History of severe hypoglycemia (such as consciousness disorder and coma caused by hypoglycemia), or history of severe unconsciousness hypoglycemia;
  • Organ transplantation history, or other acquired, congenital immune system diseases, or peripheral vascular diseases with clinical significance;
  • Have significant hyperglycemia symptoms, such as polyuria, polydipsia, accidental weight loss or dehydration;
  • Habitual diarrhea, irritable bowel syndrome, clinically significant abnormal gastric emptying (such as gastric outlet obstruction), severe chronic gastrointestinal diseases (such as active ulcer within 6 months), long-term medication with direct impact on gastrointestinal peristalsis, or gastrointestinal surgery;
  • Have obvious blood system diseases (such as aplastic anemia, myelodysplastic syndrome), or any disease causing hemolysis or red blood cell instability (such as malaria), or accompanied by hemoglobin diseases (such as sickle type red blood cell disease) that may affect the determination of HbA1c level;
  • Obvious autonomic neuropathy, such as urinary retention, orthostatic hypotension, diabetic diarrhea or gastroparesis.
  • History of heart failure (NYHA class Ⅲ and Ⅳ, Appendix 2), or history of acute myocardial infarction or unstable angina within 6 months before screening, or history of coronary angioplasty, coronary stent implantation or coronary bypass surgery within 6 months before screening, or recent cardiac surgery plan;
  • Serious trauma, infection or operation that may affect blood glucose control occurred within one month before screening;
  • In the first two months of the screening, the drug with weight control effect was used or the operation that can lead to weight instability was performed, or the drug is currently in the weight-loss plan and is not in the maintenance stage;
  • Completed or withdrawn an intervention clinical trial within 3 months before screening, or is currently conducting the intervention clinical trial, or participated in other medical research activities, which is not suitable for the study according to the judgment of the researcher;
  • Those who frequently drink alcohol (more than 21 units (male) and 14 units / week (female) (1 unit = 360ml beer; or 150ml wine; or 45ml white wine) in the three months before screening, or who can't stop drinking during the test;
  • Those who are addicted to smoking (more than 10 cigarettes per day or the same amount of tobacco) within 3 months before screening or who cannot quit smoking (stop nicotine intake) during the trial;
  • Those who lost / donated more than 400 ml blood within 3 months before screening (except female physiological blood loss), received blood transfusion or used blood products, or planned to donate blood within 1 month (30 days) after the end of the trial or during the trial;
  • To screen the patients with unstable thyroid function (such as thiourea and thyroid hormone drugs) in the first 6 months, with poor control of hypothyroidism or history of hypothyroidism;
  • In the first 6 months of screening, there was a history of diabetic acute metabolic complications (diabetic ketoacidosis, hyperosmotic nonketotic coma, diabetic lactate acidosis);
  • In the screening period, when no pacemaker was installed, 12 lead ECG showed second degree or third degree atrioventricular block or qtcb interval prolonged more than 500 ms;
  • The results of clinical laboratory examination in screening period meet any of the following criteria:

    1. Hemoglobin (Hgb) < lower limit of normal value (LLN);
    2. Aspartate transaminase (AST) or alanine transaminase (ALT) > 2 times of upper limit of normal value (ULN);
    3. Total bilirubin (TBIL) > 1.5 times the upper limit of normal value (except for known Gilbert syndrome which meets the following requirements, that is, part of bilirubin indicates that the combined bilirubin is less than 35% of total bilirubin);
    4. Triglyceride (TG) ≥ 5.7mmol/l;
    5. Estimated glomerular filtration rate < 60 ml / min (estimated by Cockroft Gault formula);
    6. Fasting C peptide < 1.0 ng / ml (333 pmol / L);
    7. Hepatitis B surface antigen, hepatitis C virus antibody, Treponema pallidum antibody or human immunodeficiency virus antibody were screened positive;
  • Poor blood pressure control (SBP ≥ 160mmhg and / or DBP ≥ 100mmhg);
  • Patients with history of needle syncope, blood syncope or intolerant of venipuncture;
  • Those with a history of drug abuse or positive drug abuse screening;
  • Patients with obvious mental disorders, epilepsy and other persons without behavioral or cognitive abilities;
  • Female subjects in pregnancy, lactation, or with pregnancy intention, or positive pregnancy test (hCG test); and female subjects of childbearing age who can not take effective contraceptive measures (effective contraceptive measures include abstinence, sterilization, intrauterine device, or diaphragm method stipulated by local laws) during the test period;
  • The subject may not complete the study for other reasons or the researcher thinks it should not be included.

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: Sekvensiell tildeling
  • Masking: Dobbelt

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: SY-008-6mg/d
2mg TID. The subjects were given the drug for the first time before breakfast in D1, and then continued to take the drug daily until dinner in D7, and left after PD sample collection and safety assessment before breakfast in D8. The researchers will decide whether to move on to the next stage,12mg/d.
The subjects were admitted to the clinical trial center two days before the administration period (D-2), fasted for 10 hours overnight on the day before the Administration (D-1), and banned water for 1 hour before the administration. Take sy-009 test drug or placebo immediately before meal (QD is before breakfast, bid is before breakfast and dinner) in the morning of the first day of administration, and deliver it with not more than 200ml warm boiled water. From the day 2 (D2) to the day 7 (D7) before dinner, the oral cavity of the subjects was checked for residual drugs after each administration.
Eksperimentell: SY-008-12mg/d
4mg TID. The subjects were given the drug for the first time before breakfast in D1, and then continued to take the drug daily until dinner in D7, and left after PD sample collection and safety assessment before breakfast in D8. The researchers will decide whether to move on to the next stage,18mg/d.
The subjects were admitted to the clinical trial center two days before the administration period (D-2), fasted for 10 hours overnight on the day before the Administration (D-1), and banned water for 1 hour before the administration. Take sy-009 test drug or placebo immediately before meal (QD is before breakfast, bid is before breakfast and dinner) in the morning of the first day of administration, and deliver it with not more than 200ml warm boiled water. From the day 2 (D2) to the day 7 (D7) before dinner, the oral cavity of the subjects was checked for residual drugs after each administration.
Eksperimentell: SY-008-18mg/d
6mg TID. The subjects were given the drug for the first time before breakfast in D1, and then continued to take the drug daily until dinner in D7, and left after PD sample collection and safety assessment before breakfast in D8, and then the test will be terminated.
The subjects were admitted to the clinical trial center two days before the administration period (D-2), fasted for 10 hours overnight on the day before the Administration (D-1), and banned water for 1 hour before the administration. Take sy-009 test drug or placebo immediately before meal (QD is before breakfast, bid is before breakfast and dinner) in the morning of the first day of administration, and deliver it with not more than 200ml warm boiled water. From the day 2 (D2) to the day 7 (D7) before dinner, the oral cavity of the subjects was checked for residual drugs after each administration.
Placebo komparator: SY-008 matching placebo
Oral administration of the same number of tablets in the corresponding test group.
SY-008 matching placebo

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Maximum postprandial (breakfast, lunch, dinner) blood glucose added value.
Tidsramme: 7 days
Compared with placebo, the maximum change in glucose from baseline at D7.
7 days
Blodglukose AUC (AUC 0-4,AUC 4-10, AUC 10-14, AUC 0-24) i ulike perioder.
Tidsramme: 7 dager
Sammenlignet med placebo, gjennomsnittlig endring i glukose AUC fra baseline ved D7.
7 dager
The Safety and tolerance of SY-009,Collecting Number of subjects with adverse events as assessed by CTCAE V5.0.
Tidsramme: 7 days
Number of subjects with adverse events, major adverse events, serious adverse events, abnormal Laboratory Values, abnormal vital signs, Abnormal physical examination, Abnormal ECG data,Gastrointestinal adverse reactions (diarrhea, etc.) and hypoglycemia events.
7 days
C-peptidkonsentrasjonen endres før og etter måltid.
Tidsramme: 7 dager
Sammenlignet med placebo, gjennomsnittlig endring fra baseline ved D7.
7 dager
Endringer i insulinkonsentrasjon før og etter måltid.
Tidsramme: 7 dager
Sammenlignet med placebo, gjennomsnittlig endring fra baseline ved D7.
7 dager
GLP-1-konsentrasjonen endres før og etter måltid.
Tidsramme: 7 dager
Sammenlignet med placebo, gjennomsnittlig endring fra baseline ved D7.
7 dager
GIP-konsentrasjonen endres før og etter måltid.
Tidsramme: 7 dager
Sammenlignet med placebo, gjennomsnittlig endring fra baseline ved D7.
7 dager

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Toppkonsentrasjon (Cmax)
Tidsramme: 1 dag
etter den første dosen
1 dag
Topptid (Tmax)
Tidsramme: 1 dag
etter den første dosen
1 dag
Terminalelimineringshastighetskonstant (λ z)
Tidsramme: 1 dag
etter den første dosen
1 dag
Terminal eliminasjonshalveringstid (T1 / 2)
Tidsramme: 1 dag
etter den første dosen
1 dag
Område under medikamenttidskurven fra 0 til siste påvisbare tidspunkt (auc0-t)
Tidsramme: 1 dag
etter den første dosen
1 dag
Areal under medikamenttidskurven (auc0 - ∞) fra 0 til uendelig tid
Tidsramme: 1 dag
etter den første dosen
1 dag
Auc0 - ∞ ekstrapoleringsprosent (% aucex)
Tidsramme: 1 dag
etter den første dosen
1 dag
Tilsynelatende klarering (CL / F)
Tidsramme: 1 dag
etter den første dosen
1 dag
Tilsynelatende distribusjonsvolum (VZ / F).
Tidsramme: 1 dag
etter den første dosen
1 dag
Steady state toppkonsentrasjon (Cmax, SS).
Tidsramme: 7 dager
Etter å ha nådd steady state
7 dager
Steady state topptid (Tmax, SS).
Tidsramme: 7 dager
Etter å ha nådd steady state
7 dager
Steady state terminal eliminasjonshalveringstid (T1 / 2, SS).
Tidsramme: 7 dager
Etter å ha nådd steady state
7 dager
Område under medikamenttidskurve (auc0-t, SS) fra steady state 0 til siste detekterbare tid.
Tidsramme: 7 dager
Etter å ha nådd steady state
7 dager
Arealet under medikamenttidskurven (auc0 - ∞, SS) med steady state fra 0 til uendelig tid.
Tidsramme: 7 dager
Etter å ha nådd steady state
7 dager
Auc0 - ∞ ekstrapoleringsprosent (% aucex)
Tidsramme: 7 dager
Etter å ha nådd steady state
7 dager
Akkumuleringsforhold (rauc, rcmax)
Tidsramme: 7 dager
Etter å ha nådd steady state
7 dager
Stabil dalkonsentrasjon (gjennomsnitt, SS).
Tidsramme: 7 dager
Etter å ha nådd steady state
7 dager

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)

15. juni 2020

Primær fullføring (Faktiske)

15. desember 2021

Studiet fullført (Faktiske)

15. desember 2021

Datoer for studieregistrering

Først innsendt

9. april 2020

Først innsendt som oppfylte QC-kriteriene

10. april 2020

Først lagt ut (Faktiske)

14. april 2020

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

18. mai 2022

Siste oppdatering sendt inn som oppfylte QC-kriteriene

17. mai 2022

Sist bekreftet

1. mai 2021

Mer informasjon

Begreper knyttet til denne studien

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

Abonnere