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A Phase 1, Double-blind, Randomized Study to Evaluate the Safety, Tolerability, Pharmacodynamics, and Pharmacokinetics of Single Dose and Multiple Doses of CG-0416 in Healthy Participants.

23 luglio 2026 aggiornato da: HongKong Curegene Innovation Co., Limited
A Phase 1, double-blind, randomized study to evaluate the safety, tolerability, pharmacodynamics, and pharmacokinetics of single dose and multiple doses of CG-0416 in healthy participants. HongKong Curegene Innovation Co. Limited is developing the study drug CG-0416 as a potential new treatment for overweight and obesity. The purpose of this research is to investigate the safety, tolerability (if any side effects occur), pharmacokinetics (the amount of study drug or any of its breakdown products in your body) and pharmacodynamics (how the study drug affects your body), of single and multiple oral doses of a study drug called CG-0416.

Panoramica dello studio

Stato

Non ancora reclutamento

Condizioni

Intervento / Trattamento

Tipo di studio

Interventistico

Iscrizione (Stimato)

64

Fase

  • Fase 1

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Backup dei contatti dello studio

Luoghi di studio

    • Victoria
      • Melbourne, Victoria, Australia, 3004

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto

Accetta volontari sani

Sì

Descrizione

Inclusion Criteria:

  1. Male and female participants aged 18 to 60 years, inclusive, at the time of screening.
  2. BMI of ≥ 18 kg/m2 to ≤ 32 kg/m2 for SAD and ≥ 21 kg/m2 to ≤ 35 kg/m2 for MAD at screening, and body weight > 50 kg for SAD and MAD.
  3. Participants will be assessed to be in good health by the investigator, such as no clinically relevant abnormalities that will affect participant safety in the opinion of the investigator based on medical history, physical examination, clinical laboratory assessments (hematology, serum chemistry, coagulation, urinalysis, TH), and 12-lead ECG.
  4. LDL-C > 1.8 mmol/L (70 mg/dL) in SAD, LDL-C > 2.6 mmol/L (100 mg/dL) in MAD.
  5. Self-reported stable weight (within ± 5% change) for at least 3 months prior to screening.
  6. Participant and his/her sexual partner are not planning to fall pregnant and male participants can't donate sperm for 95 days after the last dose of study drug and willing to use two or more effective contraception methods (contraception guidance is provided in Appendix 17.1). Women of childbearing potential (WOCBP) must have a negative serum or urine pregnancy test within 24 hours prior to the start of study drug and must not be breastfeeding, lactating or planning pregnancy during the study period. WOCBP are defined as any female who has experienced menarche and who has not undergone surgical sterilization (hysterectomy, bilateral salpingectomy or bilateral oophorectomy) and is not postmenopausal. Menopause is defined as 12 months of amenorrhea in the absence of other biological causes. In addition, females under the age of 55 years must have a documented serum FSH level > 40 mIU/mL to confirm menopause. Male participants with potentially postmenopausal partners who are under the age of 55 years must use condoms unless their partner's postmenopausal status has been confirmed by FSH level.
  7. Participants have a full understanding of the trial content, process and possible adverse reactions, and voluntarily signed the informed consent form (ICF).

Exclusion Criteria:

  1. Clinically significant infection and/or cardiovascular, hematologic, renal, hepatic, pulmonary, endocrine, gastrointestinal, immunologic, dermatologic, neurologic, current or history of ADHD, anxiety or depression, or psychiatric disease at screening that, or its treatment, may have interfered with the conduct of the study (e.g., study procedure compliance, safety assessment, study results interpretation) or, in the judgment of the investigator, will have placed the participant at an unacceptable risk if participating in the study.
  2. Clinically significant diseases (including but not limited to gastrointestinal, renal, hepatic, neurological, hematological, endocrine, neoplastic, pulmonary, immunological, psychiatric or cardiovascular disease) within 6 months before screening.
  3. Thyroid diseases: a) active hyperthyroidism; b) TSH >7 IU/L with symptoms of hypothyroidism or >10 IU/L without symptoms.
  4. Diagnosis of type 1 or 2 diabetes or other autoimmune diabetes (fully resolved gestational diabetes will be permitted).
  5. Glycated hemoglobin (HbA1c) > 6.5% or fasting blood glucose ≥ 7.0 mmol/L.
  6. Fasting (TG ≥ 500 mg/dL (or 5.65 mmol/L) at screening.
  7. Participant meets any of the following:

    1. Transaminases (AST, ALT) > 1.5 × ULN.
    2. Alkaline phosphatase (ALP) > 1.5 × ULN.
    3. Serum total bilirubin > 1.5 × ULN (participants diagnosed with Gilbert's syndrome at screening are allowed to meet all other criteria).
    4. Platelet count < 100,000/mm³.
    5. International normalized ratio (INR) > ULN (as per the local laboratory reference range).
    6. Albumin < 35 g/L.
    7. Estimated glomerular filtration rate < 60 mL/min/1.73m2 per Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) 2021 formula.
  8. Severe allergic diseases or suspected allergy to any component of the study drug, allergic constitution (multiple drug and food allergy) judged by the investigator.
  9. Any of the following abnormalities on the 12-lead ECG at screening:

    1. QTcF (Fridericia-corrected QT interval) > 450 msec for males or > 470 msec for females.
    2. In addition to the above, any clinically significant ECG abnormality, as judged by the investigator.
  10. Systolic blood pressure > 145 mmHg and diastolic blood pressure > 95 mmHg in supine position (at least 5 minutes) at screening, confirmed by retest.
  11. Use of antibiotics or immunosuppressive drugs (e.g., systemic corticosteroids) within 30 days prior to administration of CG-0416 on Day 1.
  12. Any short-term or long-term treatment for obesity within 3 months prior to screening.
  13. For use of prescription medication, within 14 days or 5 half-lives (whichever is longer) before screening with the exception of hormone replacement and contraception therapy. For use of over-the-counter (OTC) medications, food supplements (excluding routing vitamins, paracetamol, ibuprofen), weight loss and fat reduction supplements (L-carnitine, green coffee extract, chitosan, weight loss tea, yerba mate tea, meal replacement, etc.), supplements for thyroid endocrine disruption (iodine supplements, seaweed and kelp extracts, etc.), lipid-lowering supplements (fish oil, etc.) etc. 7 days before screening is sufficient (Only vitamins and other supplements that do not affect the study drug are allowed to be used. Other supplements are not permitted).
  14. Smoking > 5 cigarettes (or equivalent amount of nicotine products) per week within 30 days before the screening or inability to abstain from tobacco products during the study.
  15. Any vaccination within 14 days prior to screening or anticipated administration of a live vaccine during the study.
  16. Receipt of an investigational drug or device or participation in a drug study within 60 days (or 5 half-lives of the drug, whichever is longer) before dosing on Day 1.
  17. Positive during screening for hepatitis B surface antigen (HBsAg), hepatitis B core antibody (HBcAb), hepatitis C antibody (amplification test to confirm if positive; cured hepatitis C can be enrolled), or human immunodeficiency virus (HIV) antibody, treponema pallidum antibody.
  18. History of drug abuse within 6 months before screening, or positive drug abuse test at screening.
  19. Weekly alcohol consumption of more than 10 units of alcohol (1 unit of alcohol = 360 mL of beer or 45 mL of spirit with the alcohol content of 40% or 150 mL of wine) in any week within the past 3 months before screening; intake of alcohol-containing products within 48 hours prior to the first dose of study drug or inability to abstain from any alcohol during the study, or positive alcohol test at screening.
  20. Donation of more than 400 mL of blood or plasma within 30 days before screening or planned donation within 90 days of study treatment administration.
  21. Consumption/consumption of coffee, tea, grapefruit, chocolate or soft drinks such as cola containing methylxanthines (theophylline, caffeine or theobromine) within 48 hours before dosing.
  22. Strenuous exercise, such as weightlifting, sprinting, long-distance running, cycling, swimming, and playing soccer, is performed within 72 hours before screening and any study visit until the follow-up has been completed; if it is not within the window period before the above-mentioned screening and study visits, maintenance of daily exercise or activity plan is allowed.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione sequenziale
  • Mascheramento: Quadruplicare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Cohort 1
8 healthy participants will be randomly assigned in a ratio of 3:1 to receive a single dose of CG-0416 or placebo
CG-0416 is a novel selective, liver-directed thyroid hormone receptor beta (THR-β) agonist, given orally once daily.
Sperimentale: Cohort 2
8 healthy participants will be randomly assigned in a ratio of 3:1 to receive a single dose of CG-0416 or placebo
CG-0416 is a novel selective, liver-directed thyroid hormone receptor beta (THR-β) agonist, given orally once daily.
Sperimentale: Cohort 3
8 healthy participants will be randomly assigned in a ratio of 3:1 to receive a single dose of CG-0416 or placebo
CG-0416 is a novel selective, liver-directed thyroid hormone receptor beta (THR-β) agonist, given orally once daily.
Sperimentale: Cohort 4
8 healthy participants will be randomly assigned in a ratio of 3:1 to receive a single dose of CG-0416 or placebo
CG-0416 is a novel selective, liver-directed thyroid hormone receptor beta (THR-β) agonist, given orally once daily.
Sperimentale: Cohort 5
8 healthy participants will be randomly assigned in a ratio of 3:1 to receive a single dose of CG-0416 or placebo
CG-0416 is a novel selective, liver-directed thyroid hormone receptor beta (THR-β) agonist, given orally once daily.
Sperimentale: Cohort 1a
8 healthy participants will be randomly assigned in a ratio of 3:1 to receive a low dose of CG-0416 or placebo once daily for 14 consecutive days.
CG-0416 is a novel selective, liver-directed thyroid hormone receptor beta (THR-β) agonist, given orally once daily.
Sperimentale: Cohort 2a
8 healthy participants will be randomly assigned in a ratio of 3:1 to receive a middle dose of CG-0416 or placebo once daily for 14 consecutive days.
CG-0416 is a novel selective, liver-directed thyroid hormone receptor beta (THR-β) agonist, given orally once daily.
Sperimentale: Cohort 3a
8 healthy participants will be randomly assigned in a ratio of 3:1 to receive a high dose of CG-0416 or placebo once daily for 14 consecutive days.
CG-0416 is a novel selective, liver-directed thyroid hormone receptor beta (THR-β) agonist, given orally once daily.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
To determine number of participants with treatment-related adverse events as assessed by CTCAE v6.0 of single dose and multiple doses of CG-0416 in healthy participants.
Lasso di tempo: up to 3 weeks
Number of Incidence and frequency of adverse events (AEs) / SAEs possibly or probably related to study drug.
up to 3 weeks
To determine the safety and tolerability of single dose and multiple doses of CG-0416 in healthy participants
Lasso di tempo: up to 3 weeks
Concentration changes from baseline in clinical laboratory safety tests: thyroid hormones [TH] , thyroid-stimulating hormone (TSH), free triiodothyronine (FT3), free thyroxine (FT4)], follicle-stimulating hormone (FSH), luteinizing hormone, estradiol, testosterone, and free testosterone.
up to 3 weeks
To determine the safety and tolerability of single dose and multiple doses of CG-0416 in healthy participants.
Lasso di tempo: up to 3 weeks
Baseline and placebo-corrected QTcF (ΔΔQTcF).
up to 3 weeks

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
To define pharmacokinetics (PK) profile of CG-0416 and its active metabolite CG-0400
Lasso di tempo: up to 3 weeks
Area under the concentration-time curve from time 0 to the last measurable concentration (AUC0-last).
up to 3 weeks
To define pharmacokinetics (PK) profile of CG-0416 and its active metabolite CG-0400
Lasso di tempo: up to 3 weeks
Area under the concentration-time curve from time 0 to theoretical infinity (AUC0-inf).
up to 3 weeks
To define pharmacokinetics (PK) profile of CG-0416 and its active metabolite CG-0400
Lasso di tempo: up to 3 weeks
peak concentration (Cmax).
up to 3 weeks
To define pharmacokinetics (PK) profile of CG-0416 and its active metabolite CG-0400
Lasso di tempo: up to 3 weeks
Time to peak concentration (Tmax).
up to 3 weeks
To define pharmacokinetics (PK) profile of CG-0416 and its active metabolite CG-0400
Lasso di tempo: Up to 3 weeks
Terminal elimination half-life (T1/2).
Up to 3 weeks
To assess pharmacodynamic (PD) parameters
Lasso di tempo: up to 3 weeks
Concentration changes from baseline in fasting blood apolipoprotein B (ApoB), lipoprotein (a) [Lp(a)], low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C), total cholesterol (TC), triglyceride (TG)
up to 3 weeks
To assess pharmacodynamic (PD) parameter insulin
Lasso di tempo: up to 3 weeks
Concentration changes from baseline in insulin
up to 3 weeks
To assess pharmacodynamic (PD) parameter sex hormone binding globulin (SHBG)
Lasso di tempo: up to 3 weeks
Concentration changes from baseline in sex hormone binding globulin (SHBG).
up to 3 weeks

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Investigatori

  • Investigatore principale: Philip Ryan, MD, Nucleus Network Pty Ltd.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

1 luglio 2026

Completamento primario (Stimato)

1 marzo 2027

Completamento dello studio (Stimato)

1 aprile 2027

Date di iscrizione allo studio

Primo inviato

9 luglio 2026

Primo inviato che soddisfa i criteri di controllo qualità

23 luglio 2026

Primo Inserito (Effettivo)

24 luglio 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

24 luglio 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

23 luglio 2026

Ultimo verificato

1 luglio 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • CG-AU-0416-01

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .