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SAD Study of CGB3002 in Healthy Participants

16. Juni 2026 aktualisiert von: 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.

Studienübersicht

Detaillierte Beschreibung

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.

Studientyp

Interventionell

Einschreibung (Geschätzt)

46

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

Studienorte

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

  • Erwachsene

Akzeptiert gesunde Freiwillige

Ja

Beschreibung

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.

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: Doppelt

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Placebo-Komparator: 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.
Aktiver Komparator: 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.
Experimental: 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.
Experimental: 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.
Experimental: 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.
Experimental: 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.
Experimental: 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.

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Percentage of Participants with Adverse Events as a Measure of Safety and Tolerability
Zeitfenster: 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.

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
PK of CGB3002: Maximum Concentration (Cmax)
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: 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
Zeitfenster: 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)
Zeitfenster: 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

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Ermittler

  • Studienleiter: Zhizheng Zhang, M.D., ChainGen Biopharma Ltd

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 (Geschätzt)

30. Juni 2026

Primärer Abschluss (Geschätzt)

30. April 2027

Studienabschluss (Geschätzt)

30. April 2027

Studienanmeldedaten

Zuerst eingereicht

16. Juni 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

16. Juni 2026

Zuerst gepostet (Tatsächlich)

22. Juni 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

22. Juni 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

16. Juni 2026

Zuletzt verifiziert

1. Juni 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Andere Studien-ID-Nummern

  • CGB3002-RT01

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

Produkt, das in den USA hergestellt und aus den USA exportiert wird

Nein

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