SAD Study of CGB3002 in Healthy Participants
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
Studie Overzicht
Toestand
Toestand
Conditie
Conditie
Interventie / Behandeling
Interventie / Behandeling
Gedetailleerde beschrijving
Studietype
Studietype
Inschrijving (Geschat)
Inschrijving
Fase
Fase
- Fase 1
Contacten en locaties
Studiecontact
Studiecontact
- Naam: Ofer Gonen, M.D.
- Telefoonnummer: (03) 8593 9801
- E-mail: o.gonen@nucleusnetwork.com.au
Studie Locaties
-
-
Victoria
-
Melbourne, Victoria, Australië, 3004
- Werving
- Nucleus Network
-
Contact:
- Nucleus Network Melbourne
- Telefoonnummer: 1800 243 733
- E-mail: melbourne@nucleusnetwork.com
-
-
Deelname Criteria
Geschiktheidscriteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Volwassen
Accepteert gezonde vrijwilligers
Beschrijving
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.
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Dubbele
Aantal wapens
Wapens en interventies
Deelnemersgroep / ArmDeelnemersgroep / Arm |
Interventie / BehandelingInterventie / Behandeling |
|---|---|
|
Placebo-vergelijker: 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.
|
|
Actieve vergelijker: 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.
|
|
Experimenteel: 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.
|
|
Experimenteel: 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.
|
|
Experimenteel: 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.
|
|
Experimenteel: 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.
|
|
Experimenteel: 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.
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Percentage of Participants with Adverse Events as a Measure of Safety and Tolerability
Tijdsspanne: 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.
|
Secundaire uitkomstmaten
Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
PK of CGB3002: Maximum Concentration (Cmax)
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: 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)
Tijdsspanne: 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
Tijdsspanne: 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)
Tijdsspanne: 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
|
Medewerkers en onderzoekers
Sponsor
Sponsor
Medewerkers
Medewerkers
Onderzoekers
Onderzoekers
- Studie directeur: Zhizheng Zhang, M.D., ChainGen Biopharma Ltd
Studie record data
Bestudeer belangrijke data
Studie start (Werkelijk)
Studie start
Primaire voltooiing (Geschat)
Primaire voltooiing
Studie voltooiing (Geschat)
Studie voltooiing
Studieregistratiedata
Eerst ingediend
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Eerst geplaatst
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update geplaatst
Laatste update ingediend die voldeed aan QC-criteria
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Andere studie-ID-nummers
Andere studie-ID-nummers
- CGB3002-RT01
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
Informatie over medicijnen en apparaten, studiedocumenten
Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel
Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct
product vervaardigd in en geëxporteerd uit de V.S.
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .