- ICH GCP
- Yhdysvaltain kliinisten tutkimusten rekisteri
- Kliininen tutkimus NCT04345120
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
Tutkimuksen yleiskatsaus
Tila
Interventio / Hoito
Yksityiskohtainen kuvaus
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.
Opintotyyppi
Ilmoittautuminen (Todellinen)
Vaihe
- Vaihe 1
Yhteystiedot ja paikat
Opiskelupaikat
-
-
Jiangsu
-
Nanjing, Jiangsu, Kiina, 210093
- Nanjing Gulou Hospital
-
-
Osallistumiskriteerit
Kelpoisuusvaatimukset
Opintokelpoiset iät
Hyväksyy terveitä vapaaehtoisia
Sukupuolet, jotka voivat opiskella
Kuvaus
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:
- Hemoglobin (Hgb) < lower limit of normal value (LLN);
- Aspartate transaminase (AST) or alanine transaminase (ALT) > 2 times of upper limit of normal value (ULN);
- 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);
- Triglyceride (TG) ≥ 5.7mmol/l;
- Estimated glomerular filtration rate < 60 ml / min (estimated by Cockroft Gault formula);
- Fasting C peptide < 1.0 ng / ml (333 pmol / L);
- 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.
Opintosuunnitelma
Miten tutkimus on suunniteltu?
Suunnittelun yksityiskohdat
- Ensisijainen käyttötarkoitus: Hoito
- Jako: Satunnaistettu
- Inventiomalli: Peräkkäinen tehtävä
- Naamiointi: Kaksinkertainen
Aseet ja interventiot
Osallistujaryhmä / Arm |
Interventio / Hoito |
|---|---|
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Kokeellinen: 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.
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Kokeellinen: 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.
|
|
Kokeellinen: 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.
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Placebo Comparator: SY-008 matching placebo
Oral administration of the same number of tablets in the corresponding test group.
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SY-008 matching placebo
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Mitä tutkimuksessa mitataan?
Ensisijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
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Maximum postprandial (breakfast, lunch, dinner) blood glucose added value.
Aikaikkuna: 7 days
|
Compared with placebo, the maximum change in glucose from baseline at D7.
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7 days
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Verensokerin AUC (AUC 0-4, AUC 4-10, AUC 10-14, AUC 0-24) eri ajanjaksoina.
Aikaikkuna: 7 päivää
|
Verrattuna lumelääkkeeseen glukoosin AUC:n keskimääräinen muutos lähtötilanteesta 7. päivänä.
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7 päivää
|
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The Safety and tolerance of SY-009,Collecting Number of subjects with adverse events as assessed by CTCAE V5.0.
Aikaikkuna: 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.
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7 days
|
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C-peptidipitoisuus muuttuu ennen ateriaa ja sen jälkeen.
Aikaikkuna: 7 päivää
|
Plaseboon verrattuna keskimääräinen muutos lähtötilanteesta päivänä 7.
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7 päivää
|
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Insuliinipitoisuuden muutokset ennen ateriaa ja sen jälkeen.
Aikaikkuna: 7 päivää
|
Plaseboon verrattuna keskimääräinen muutos lähtötilanteesta päivänä 7.
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7 päivää
|
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GLP-1-pitoisuus muuttuu ennen ateriaa ja sen jälkeen.
Aikaikkuna: 7 päivää
|
Plaseboon verrattuna keskimääräinen muutos lähtötilanteesta päivänä 7.
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7 päivää
|
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GIP-pitoisuus muuttuu ennen ateriaa ja sen jälkeen.
Aikaikkuna: 7 päivää
|
Plaseboon verrattuna keskimääräinen muutos lähtötilanteesta päivänä 7.
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7 päivää
|
Toissijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
|
Huippupitoisuus (Cmax)
Aikaikkuna: 1 päivä
|
ensimmäisen annoksen jälkeen
|
1 päivä
|
|
Huippuaika (Tmax)
Aikaikkuna: 1 päivä
|
ensimmäisen annoksen jälkeen
|
1 päivä
|
|
Päätteen eliminointinopeusvakio (λ z)
Aikaikkuna: 1 päivä
|
ensimmäisen annoksen jälkeen
|
1 päivä
|
|
Terminaalinen eliminaation puoliintumisaika (T1/2)
Aikaikkuna: 1 päivä
|
ensimmäisen annoksen jälkeen
|
1 päivä
|
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Lääkeaikakäyrän alla oleva pinta-ala 0:sta viimeiseen havaittavissa olevaan aikaan (auc0-t)
Aikaikkuna: 1 päivä
|
ensimmäisen annoksen jälkeen
|
1 päivä
|
|
Lääkeaikakäyrän alla oleva pinta-ala (auc0 - ∞) 0:sta äärettömään aikaan
Aikaikkuna: 1 päivä
|
ensimmäisen annoksen jälkeen
|
1 päivä
|
|
Auc0 - ∞ ekstrapolointiprosentti (% aucex)
Aikaikkuna: 1 päivä
|
ensimmäisen annoksen jälkeen
|
1 päivä
|
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Näennäinen välys (CL / F)
Aikaikkuna: 1 päivä
|
ensimmäisen annoksen jälkeen
|
1 päivä
|
|
Näennäinen jakautumistilavuus (VZ / F).
Aikaikkuna: 1 päivä
|
ensimmäisen annoksen jälkeen
|
1 päivä
|
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Vakaan tilan huippupitoisuus (Cmax, SS).
Aikaikkuna: 7 päivää
|
Vakaan tilan saavuttamisen jälkeen
|
7 päivää
|
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Vakaan tilan huippuaika (Tmax, SS).
Aikaikkuna: 7 päivää
|
Vakaan tilan saavuttamisen jälkeen
|
7 päivää
|
|
Vakaan tilan terminaalinen eliminaation puoliintumisaika (T1/2, SS).
Aikaikkuna: 7 päivää
|
Vakaan tilan saavuttamisen jälkeen
|
7 päivää
|
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Lääkkeen aikakäyrän alla oleva alue (auc0-t, SS) vakaasta tilasta 0 viimeiseen havaittavissa olevaan aikaan.
Aikaikkuna: 7 päivää
|
Vakaan tilan saavuttamisen jälkeen
|
7 päivää
|
|
Lääkkeen aikakäyrän alla oleva alue (auc0 - ∞, SS) vakaassa tilassa 0:sta äärettömään aikaan.
Aikaikkuna: 7 päivää
|
Vakaan tilan saavuttamisen jälkeen
|
7 päivää
|
|
Auc0 - ∞ ekstrapolointiprosentti (% aucex)
Aikaikkuna: 7 päivää
|
Vakaan tilan saavuttamisen jälkeen
|
7 päivää
|
|
Akkumulaatiosuhde (rauc, rcmax)
Aikaikkuna: 7 päivää
|
Vakaan tilan saavuttamisen jälkeen
|
7 päivää
|
|
Vakaa laakson pitoisuus (Ctrough, SS).
Aikaikkuna: 7 päivää
|
Vakaan tilan saavuttamisen jälkeen
|
7 päivää
|
Yhteistyökumppanit ja tutkijat
Opintojen ennätyspäivät
Opi tärkeimmät päivämäärät
Opiskelun aloitus (Todellinen)
Ensisijainen valmistuminen (Todellinen)
Opintojen valmistuminen (Todellinen)
Opintoihin ilmoittautumispäivät
Ensimmäinen lähetetty
Ensimmäinen toimitettu, joka täytti QC-kriteerit
Ensimmäinen Lähetetty (Todellinen)
Tutkimustietojen päivitykset
Viimeisin päivitys julkaistu (Todellinen)
Viimeisin lähetetty päivitys, joka täytti QC-kriteerit
Viimeksi vahvistettu
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