- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT04790006
A Study of TG103 in Subjects With Type 2 Diabetes
7. März 2021 aktualisiert von: CSPC ZhongQi Pharmaceutical Technology Co., Ltd.
A Randomized, Double-blind, Placebo-controlled, Multicenter, Multiple Ascending Dose Phase Ib Study in Subjects With Type 2 Diabetes to Evaluate the Safety, Tolerability and Pharmacokinetic Profile of TG103 Injection
The main purpose of this study is to assess the safety and tolerability of multiple ascending doses of TG103 in subjects with type 2 diabetes.
Studienübersicht
Status
Noch keine Rekrutierung
Bedingungen
Intervention / Behandlung
Detaillierte Beschreibung
This study is a randomized, double-blind, placebo-controlled, multicenter, dose-escalating study to characterize the safety (including the anti-drug antibodies(ADA)), tolerability pharmacokinetics (PK) and pharmacodynamic parameters(PD)of TG103.
The study will consist of 3 periods: an approximately 2-week lead-in period, followed by a 12-week treatment period, and a 3-week safety follow-up period.
Three dose groups (7.5mg, 15mg and 22.5mg) of subjects will be enrolled and dosed sequentially; 12
Studientyp
Interventionell
Einschreibung (Voraussichtlich)
54
Phase
- Phase 1
Kontakte und Standorte
Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.
Studienkontakt
- Name: Jiaoran Song
- Telefonnummer: 0311-69085931
- E-Mail: songjiaoran@mail.ecspc.com
Teilnahmekriterien
Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.
Zulassungskriterien
Studienberechtigtes Alter
18 Jahre bis 75 Jahre (Erwachsene, Älterer Erwachsener)
Akzeptiert gesunde Freiwillige
Nein
Studienberechtigte Geschlechter
Alle
Beschreibung
Inclusion Criteria:
- 1. Subjects who fully understand the test content and possible adverse reactions and voluntarily participate in the trial and sign the informed consent form;
- 2.Age: 18 to 75 years of age inclusive; no gender limitation;
- 3. Weight:body mass index (BMI) within the range of 18.5-35 kg/m2 (inclusive), BMI = weight (kg) / height 2 (m2);
- 4. Patients have diagnosed with type 2 diabetes ≤ 3 years according to the World Health Organization (WHO1999) classification; and not on medication or without a history of regular medication for more than 1 week in the 3 months prior to screening (subjects with a history of medication only include those with a history of oral medication and a history of short-term intensive insulin therapy (≤ 2 weeks));
- 5. 7.0% ≤ HbA1c ≤ 10.0%;
- 6. Subjects of childbearing potential must use reliable methods of contraception from the date of signing an informed consent to at least 3 months after the last dose;
- 7. The subject has the ability to communicate properly with the researcher and willing to fully comply with the research protocol.
Exclusion Criteria:
- 1. Fasting plasma glucose ≥13.9mmol/L or a history of severe hypoglycemia (blood sugar below 2.2mmol/L);
- 2. Systolic blood pressure ≥160 mmHg or diastolic blood pressure ≥100 mmHg during screening;
- 3. During the screening period, the white blood cell count fall outside the reference range by 10%, or hemoglobin<100g / L;
- 4. Have one or more positive tests in Hepatitis B surface antigen, hepatitis C virus antibody, anti-human immunodeficiency virus antibody or anti- Treponema pallidum-specific antibody;
- 5. Aspartate aminotransferase(AST) or Alanine aminotransferase (ALT) > 2.5x upper limit of normal (ULN), or triglyceride > 5.7mmol/L or eGFR<60 mL/(min*1.73 m2)during the screening period;
- 6. Hypercortisolism, polycystic ovary syndrome, abnormal thyroid function (those who need to be given medication or who have not reached clinical stability after treatment and whose medication still needs to be adjusted), etc. or other diseases that may affect blood glucose metabolism.
- 7. Have a personal or family history of medullary thyroid carcinoma (MTC) or type 2 multiple endocrine neoplasia, or other genetic diseases that are susceptible to medullary cancer; personal or family history of medullary thyroid carcinoma (MTC) or type 2 multiple endocrine neoplasia, or other genetic diseases that are susceptible to medullary cancer;
- 8. Acute complications of diabetes (including diabetic ketoacidosis, hyperosmolar nonketotic diabetic coma, lactic acidosis and hypoglycemia coma);
- 9. Proliferative diabetic retinopathy, foot ulcers/gangrene, and manifestations of peripheral neuropathy with obvious symptoms (e.g., gastroparesis, urinary retention, intestinal obstruction, urinary incontinence, and painful peripheral neuropathy);
- 10. Lost more than 400 ml of blood due to blood donation or other reasons within 3 months before the screening period;
- 11. During 3 months prior to screening through the entire study period, subjects used or plan to use drugs that may affect blood glucose metabolism or directly reduce gastrointestinal motility (e.g., anticholinergic drugs, antispasmodic, 5-HT3 antagonists, dopamine antagonists, and opioids), or oral and intramuscular injections of systemic corticosteroids, or inhalation or intranasal use of potent steroidal drugs with high systemic absorption; subjects regularly used thiazide diuretics within the 3 months prior to screening (Continuous medication > 1 week), or will use high doses of thiazide diuretics during the study period (hydrochlorothiazide>100 mg/d, chlorothiazide> 2 g/d, indapamide> 5 mg/d, chlorthalidone> 100 mg/d);
- 12. During the screening period, subjects with second degree or third degree atrioventricular block (except for subjects who use the pacemaker), long QT syndrome or prolonged QTc interval (male>450ms, female>470ms), or those with significant clinical symptoms of ischemic heart disease; or those with other heart diseases that are judged by the investigator to be unsuitable for entry into the study;
- 13. Any of the following cardiovascular and cerebrovascular events within half a year before screening: unstable angina pectoris requiring hospitalization, myocardial infarction, coronary artery bypass grafting, percutaneous coronary intervention (diagnostic angiography is allowed), moderate to severe congestive heart failure (NYHA grade III or IV), atrial or ventricular arrhythmia requiring hospitalization (such as atrial fibrillation and ventricular tachycardia). Subjects with pacemaker or defibrillator implantation, transient ischemic attack or cerebrovascular accident (e.g. stroke), or those with coronary artery bypass grafting or revascularization planned during the study period;
- 14. Have chronic or acute pancreatitis ( or have a history of chronic pancreatitis or acute pancreatitis) or severe gastrointestinal disease, such as confirmed reflux esophagitis or gallbladder disease, or any impact on gastric emptying (such as gastric bypass surgery, pyloric stenosis, except for appendectomy) or gastrointestinal diseases that may be aggravated by GLP-1 analogues; for patients with a history of gallbladder stones (gallstone removal or lithotripsy) and/or cholecystectomy, if there are no further sequelae, the entering of the study will be determined by researchers after assessing the risk;
- 15.Have a history of severe respiratory, blood system, and central nervous system (e.g. epilepsy) diseases; or have a history of malignant tumors or mental illnesses (such as depression, anxiety, etc.); or have other medical conditions that may endanger the safety of the subject and the investigator believes it is not suitable for inclusion;
- 16. Have had undergone major surgery within 3 months before screening, or had ongoing severe or acute infection within 4 weeks before screening;
- 17. Have a serious history of drug or food allergy, or may be allergic to the investigational product according to the judgment of the researcher;
- 18. Have taken prescription or over-the-counter medications for weight loss (e.g., orlistat, sibutramine, rimonabant, phenylpropanolamine, or chlorambucil) within 3 months prior to screening; or have undergone surgery that can cause weight instability; or have had a significant change in weight (>10% change);
- 19. Average alcohol intake is more than 21 units of alcohol (male)/14 units of alcohol (female) per week (1 unit ≈ 360mL beer, or 45mL spirits with 40% alcohol content, or 150mL wine) within the 3 months prior to screening;
- 20. Regularly consumption of caffeine is more than 600 mg of per day within the 3 months prior to screening (1 cup of coffee contains about 100 mg of caffeine, 1 cup of tea contains about 30 mg of caffeine, and 1 can of cola contains about 20 mg of caffeine);
- 21. Smoke more than 20 cigarettes per day within 3 months prior to screening;
- 22. Have skin abnormalities (such as: dermatitis) within a radius of 2cm of the administration site;
- 23.Participated in other clinical trial involving an investigational product within 3 months before the screening and the time of the last dose of the study drug is less than 3 months before the screening of this trial; or subjects withdrawn from the previous study due to an adverse event; or plan to participate other clinical trial during the study period;
- 24. Pregnant (blood pregnancy test positive in screening period) and lactating female;
- 25. Not suitable for this study in the researcher's opinion.
Studienplan
Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Vervierfachen
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Experimental: TG103
TG103 will be administered via subcutaneous injection once weekly in subjects with type 2 diabetes.
|
SC verabreicht
|
|
Placebo-Komparator: Placebo
Placebo will be administered via subcutaneous injection once weekly in subjects with type 2 diabetes.
|
SC verabreicht
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Safety and tolerability assessed by incidence and severity of adverse events
Zeitfenster: up to 15 weeks
|
A summary of SAEs and other non-serious adverse events (AEs), regardless of causality, will be reported in the Reported Adverse Events module
|
up to 15 weeks
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Area under the plasma concentration versus time curve (AUC)
Zeitfenster: Day1, 8, 15, 22, 29, 36, 43, 50, 57, 64, 71, and 78
|
PK parameters after administration of of TG103
|
Day1, 8, 15, 22, 29, 36, 43, 50, 57, 64, 71, and 78
|
|
glycosylated hemoglobin (HbA1c)
Zeitfenster: Day15, 29, 43, 57,71, and 78,
|
Pharmacodynamic (PD) parameters after administration of of TG103
|
Day15, 29, 43, 57,71, and 78,
|
|
The occurrence of TG103 anti-drug antibodies (ADA)
Zeitfenster: up to 15 weeks
|
AD Aafter administration of of TG103
|
up to 15 weeks
|
|
Peak Plasma Concentration (Cmax),
Zeitfenster: Day1, 8, 15, 22, 29, 36, 43, 50, 57, 64, 71, and 78
|
PK parameters after administration of of TG103
|
Day1, 8, 15, 22, 29, 36, 43, 50, 57, 64, 71, and 78
|
|
Time to maximum plasma concentration (Tmax)
Zeitfenster: Day1, 8, 15, 22, 29, 36, 43, 50, 57, 64, 71, and 78
|
PK parameters after administration of of TG103
|
Day1, 8, 15, 22, 29, 36, 43, 50, 57, 64, 71, and 78
|
|
Half time (t1/2),
Zeitfenster: Day1, 8, 15, 22, 29, 36, 43, 50, 57, 64, 71, and 78
|
PK parameters after administration of of TG103
|
Day1, 8, 15, 22, 29, 36, 43, 50, 57, 64, 71, and 78
|
|
Apparent clearance (CL/F)
Zeitfenster: Day1, 8, 15, 22, 29, 36, 43, 50, 57, 64, 71, and 78
|
PK parameters after administration of of TG103
|
Day1, 8, 15, 22, 29, 36, 43, 50, 57, 64, 71, and 78
|
Mitarbeiter und Ermittler
Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.
Ermittler
- Hauptermittler: Wenying Yang, China-Japan Friendship Hospital
Studienaufzeichnungsdaten
Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.
Haupttermine studieren
Studienbeginn (Voraussichtlich)
1. April 2021
Primärer Abschluss (Voraussichtlich)
1. März 2022
Studienabschluss (Voraussichtlich)
1. März 2022
Studienanmeldedaten
Zuerst eingereicht
3. März 2021
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
7. März 2021
Zuerst gepostet (Tatsächlich)
10. März 2021
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
10. März 2021
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
7. März 2021
Zuletzt verifiziert
1. März 2021
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- SYSA1803-CSP-003
Plan für individuelle Teilnehmerdaten (IPD)
Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?
Nein
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Nein
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
Nein
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