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
Studieoversigt
Status
Status
Betingelser
Betingelser
Intervention / Behandling
Intervention / Behandling
Detaljeret beskrivelse
Undersøgelsestype
Undersøgelsestype
Tilmelding (Anslået)
Tilmelding
Fase
Fase
- Fase 1
Kontakter og lokationer
Studiekontakt
Studiekontakt
- Navn: Ofer Gonen, M.D.
- Telefonnummer: (03) 8593 9801
- E-mail: o.gonen@nucleusnetwork.com.au
Studiesteder
-
-
Victoria
-
Melbourne, Victoria, Australien, 3004
- Nucleus Network
-
Kontakt:
- Nucleus Network Melbourne
- Telefonnummer: 1800 243 733
- E-mail: melbourne@nucleusnetwork.com
-
-
Deltagelseskriterier
Berettigelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
- Voksen
Tager imod sunde frivillige
Beskrivelse
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.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Dobbelt
Antal våben
Våben og indgreb
Deltagergruppe / ArmDeltagergruppe / Arm |
Intervention / BehandlingIntervention / Behandling |
|---|---|
|
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.
|
|
Aktiv 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.
|
|
Eksperimentel: 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.
|
|
Eksperimentel: 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.
|
|
Eksperimentel: 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.
|
|
Eksperimentel: 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.
|
|
Eksperimentel: 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.
|
Hvad måler undersøgelsen?
Primære resultatmål
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Percentage of Participants with Adverse Events as a Measure of Safety and Tolerability
Tidsramme: 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.
|
Sekundære resultatmål
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
PK of CGB3002: Maximum Concentration (Cmax)
Tidsramme: 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)
Tidsramme: 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)
Tidsramme: 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)
Tidsramme: 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)
Tidsramme: 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)
Tidsramme: 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)
Tidsramme: 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
Tidsramme: 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)
Tidsramme: 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
|
Samarbejdspartnere og efterforskere
Sponsor
Sponsor
Samarbejdspartnere
Samarbejdspartnere
Efterforskere
Efterforskere
- Studieleder: Zhizheng Zhang, M.D., ChainGen Biopharma Ltd
Datoer for undersøgelser
Studer store datoer
Studiestart (Anslået)
Studiestart
Primær færdiggørelse (Anslået)
Primær færdiggørelse
Studieafslutning (Anslået)
Studieafslutning
Datoer for studieregistrering
Først indsendt
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Først opslået
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering sendt
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Andre undersøgelses-id-numre
Andre undersøgelses-id-numre
- CGB3002-RT01
Plan for individuelle deltagerdata (IPD)
Planlægger du at dele individuelle deltagerdata (IPD)?
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
Studerer et amerikansk FDA-reguleret lægemiddelprodukt
Studerer et amerikansk FDA-reguleret enhedsprodukt
produkt fremstillet i og eksporteret fra U.S.A.
Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .
Kliniske forsøg med Alzheimers sygdom
-
NCT05006612AfsluttetU/S guidet SAB VS U/S guidet SAB kombineret med modificeret brystnerveblok
-
NCT05994794AfsluttetForhøjet S-adenosylhomocystein
-
NCT02589067AfsluttetS. Aureus Oropharyngeal kolonisering
-
NCT06427005RekrutteringFruquintinib | S-1 | Raltitrexed
-
NCT05242081RekrutteringOpioidbrug, uspecificeret | S-ketamin
-
NCT00748176Afsluttet
-
NCT07024576Ikke rekrutterer endnuDupuytren & amp;#39; s kontraktur | Dupuytren & amp;#39; s fasciektomi | Dupuytren & amp;#39; s sygdom
-
NCT01791127AfsluttetSiello S Leads sikkerhed og effektivitet
-
NCT07157839RekrutteringAlzheimer & amp;#39; s sygdom
-
NCT02598908UkendtEkstern kvalitetskontrol | Thiopurin S-methyl transferase (TPMT)
Kliniske forsøg med Placebo
-
NCT03827590UkendtAkut bronkitis | Akut øvre luftvejsinfektion
-
NCT02177513Afsluttet
-
NCT06767540Ikke rekrutterer endnu
-
NCT02935712AfsluttetMandlige forsøgspersoner med type II-diabetes (T2DM)
-
NCT07624383Ikke rekrutterer endnu
-
NCT03198624AfsluttetFarmakokinetik | Sikkerhedsproblemer
-
NCT01872572Afsluttet