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SAD Study of CGB3002 in Healthy Participants

16 juin 2026 mis à jour par: ChainGen Biopharma Ltd

A Randomized, Double-blind, Placebo-controlled, Phase I Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Immunogenicity of Single Ascending Doses of CGB3002 in Healthy Participants

This is a randomized, double-blind, placebo-controlled phase I clinical study to evaluate the safety, tolerability, pharmacokinetics and immunogenicity of single ascending IV doses of CGB3002 in healthy participants. CGB3002 is being developed to treat Alzheimer's Disease.

Aperçu de l'étude

Description détaillée

This study includes 5 planned sequential cohorts. Participants will be randomized to receive a single IV dose of CGB3002, active comparator or placebo, with doses administered in ascending order. Based on the emerging data, there will be options to adjust the number of participants on active or placebo per subsequent dose level, and doses may be repeated or adjusted based on safety, tolerability and plasma pharmacokinetic data. Optional cohorts may be added to evaluate an intermediate dose level or to expand the dose level by SRC.

Type d'étude

Interventionnel

Inscription (Estimé)

46

Phase

  • La phase 1

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

Lieux d'étude

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Adulte

Accepte les volontaires sains

Oui

La description

Inclusion Criteria:

  • Must have signed written informed consent before any study-related activities are carried out and must be able to understand the full nature and purpose of the trial, including possible risks and adverse effects. Be willing and able to comply with all study assessments and adhere to the protocol schedule and restrictions.
  • Age≥18 years and<55 years at the time of consent, healthy participants, male or female.
  • A body mass index (BMI) of 18 to 32 kg/m2 (cutoff inclusive), with male participants weighing no less than 50 kg, female participants weighing no less than 40 kg.
  • Males and females of childbearing potential agree to have no plans for childbearing, use reliable contraceptive measures and not to donate sperm or ova from 30 days prior to dosing until 120 days after dosing. For females of childbearing potential, hormonal contraceptives should begin at least 1 month prior to screening to ensure contraceptive is in full effect.

Exclusion Criteria:

  • A known history of clinically significant drug allergy or atopic allergic disease (asthma, urticaria, eczematous dermatitis) or a known history of allergy to biologics or any excipients in biologics, fully resolved childhood asthma can be enrolled.
  • Any disease that may affect the safety evaluation of the participants or the in vivo process of the investigational product, including the central nervous system, cardiovascular system, digestive system, respiratory system, urinary system, hematopoietic system, metabolic endocrine system, etc.
  • Use of prescription drugs within 14 days or five half-lives (whichever is longer) prior study drug administration, unless determined by the Investigator and Sponsor to be non-interfering (e.g., hormonal contraceptives).
  • Use of over-the-counter (OTC) or Chinese herbal medicine within 7 days or 5 half-lives (whichever is longer) prior to study drug administration, unless determined by the Investigator and Sponsor to be non-interfering.
  • With a history of drug abuse within 12 months prior to dosing.
  • Cannot tolerate punction, have a history of needle fainting or blood fainting.
  • Have participated in clinical trials, whether for drugs or medical devices, within 30 days prior to administration or within 7 times the known elimination half-life, whichever is longer.
  • Blood donation or significant blood loss (> 300 mL) within 30 days prior to dosing, and planning to blood donate during the study.
  • Any vaccinations with a live vaccine (excluding influenza vaccine) within 60 days prior to dosing.
  • Aspartate aminotransferase (AST) or alanine aminotransferase (ALT) ≥1.5×ULN at screening or Day -2. Total bilirubin (TBIL) > ULN at screening or Day -2(except in those due to findings consistent with Gilbert's disease).
  • Estimated creatinine clearance < 80 mL/ min (Cockroft-Gault equation) at screening or Day-2.
  • Test positive for syphilis, hepatitis B virus surface antigen (HbsAg), hepatitis B core antibody (HBcAb), hepatitis C virus antibody (HCV-Ab) or HIV antibody at screening.
  • Urine drug screening positive at screening or Day-2.
  • Have a head MRI demonstrating either cerebral microhemorrhages, or superficial siderosis, or prior evidence of microhemorrhage, or any other major intracranial pathology.
  • Still needed or planned to engage in vigorous physical activity or exercise during study participation.
  • Other conditions deemed inappropriate by the investigator to participate in the clinical trial.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Double

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Comparateur placebo: Placebo
Cohorts 1-5 each has 2 participants who will receive placebo, 10 in total.
Healthy participants will be administered a single intravenous dose of matching placebo.
Comparateur actif: Active Comparator
Cohorts 1-5 each has 2 participants will receive active comparator, 10 in total.
Healthy participants will receive a single intravenous dose of the comparator drug at the same dose level as CGB3002.
Expérimental: CGB3002 0.08 mg/kg
Healthy participants will be administered a single intravenous dose of CGB3002 (0.08 mg/kg).
Cohorts 1: healthy participants will be administered a single intravenous dose of CGB3002 at dose level of 0.08 mg/kg.
Expérimental: CGB3002 0.4 mg/kg
Healthy participants will be administered a single intravenous dose of CGB3002 (0.4 mg/kg).
Cohorts 2: healthy participants will be administered a single intravenous dose of CGB3002 at dose level of 0.4 mg/kg.
Expérimental: CGB3002 1.2 mg/kg
Healthy participants will be administered a single intravenous dose of CGB3002 (1.2 mg/kg).
Cohorts 3: healthy participants will be administered a single intravenous dose of CGB3002 at dose level of 1.2 mg/kg.
Expérimental: CGB3002 3.6 mg/kg
Healthy participants will be administered a single intravenous dose of CGB3002 (3.6 mg/kg).
Cohorts 4: healthy participants will be administered a single intravenous dose of CGB3002 at dose level of 3.6 mg/kg.
Expérimental: CGB3002 7.2 mg/kg
Healthy participants will be administered a single intravenous dose of CGB3002 (7.2 mg/kg).
Cohorts 5: healthy participants will be administered a single intravenous dose of CGB3002 at dose level of 7.2 mg/kg.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Percentage of Participants with Adverse Events as a Measure of Safety and Tolerability
Délai: up to Day 15 weeks.
Safety assessment variables will include all adverse events (AEs) including AEs, physical examinations, neurological examinations, vital sign measurements, electrocardiograms, laboratory parameters.
up to Day 15 weeks.

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
PK of CGB3002: Maximum Concentration (Cmax)
Délai: up to 8 weeks
Cmax after single intravenous infusion of CGB3002 based on non-compartmental analysis.
up to 8 weeks
PK of CGB3002: time attain to Cmax (Tmax)
Délai: up to 8 weeks
Tmax after single intravenous infusion of CGB3002 based on non-compartmental analysis.
up to 8 weeks
PK of CGB3002: Apparent terminal half-life (T1/2)
Délai: up to 8 weeks
T1/2 after single intravenous infusion of CGB3002 based on non-compartmental analysis.
up to 8 weeks
PK of CGB3002: Area under the plasma concentration versus time curve from zero to t h post-dose (AUC0-t)
Délai: up to 8 weeks
AUC0-t after single intravenous infusion of CGB3002 based on non-compartmental analysis.
up to 8 weeks
PK of CGB3002: Area under the plasma concentration versus time curve extrapolated to infinity (AUC0-inf)
Délai: up to 8 weeks
AUC0-inf after single intravenous infusion of CGB3002 based on non-compartmental analysis.
up to 8 weeks
PK of CGB3002: the total body clearance (CL)
Délai: up to 8 weeks
CL after single intravenous infusion of CGB3002 based on non-compartmental analysis.
up to 8 weeks
PK of CGB3002: Volume of distribution during the terminal phase (Vz)
Délai: up to 8 weeks
Vz after single intravenous infusion of CGB3002 based on non-compartmental analysis.
up to 8 weeks
Concentration ratio of CSF to plasma
Délai: Day 3
CSF concentrations were measured by a specific and validated method. Concentration ratio of CSF to plasma on Day 3 post dose will be calculated.
Day 3
Incidence of anti-CGB3002 antibodies (ADAs)
Délai: up to 8 weeks
For each dose group, the numbers and proportions of participants who were positive or negative for anti-drug antibodies (ADA) at baseline (baseline prevalence) and after study drug administration (post-baseline incidence during the treatment and follow-up periods) were summarized.
up to 8 weeks

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Les enquêteurs

  • Directeur d'études: Zhizheng Zhang, M.D., ChainGen Biopharma Ltd

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Estimé)

30 juin 2026

Achèvement primaire (Estimé)

30 avril 2027

Achèvement de l'étude (Estimé)

30 avril 2027

Dates d'inscription aux études

Première soumission

16 juin 2026

Première soumission répondant aux critères de contrôle qualité

16 juin 2026

Première publication (Réel)

22 juin 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

22 juin 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

16 juin 2026

Dernière vérification

1 juin 2026

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • CGB3002-RT01

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

NON

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

produit fabriqué et exporté des États-Unis.

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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