Safety and Tolerability of BDB-001 Injection in Healthy Subjects
A Randomized, Double-blind,Placebo-controlled,Single-Ascending Dose Phase Ⅰ Study to Evaluate the Safety,Tolerability,and Pharmacokinetics of BDB-001 Injection in Healthy Subjects
Studieoversigt
Status
Status
Betingelser
Betingelser
Intervention / Behandling
Intervention / Behandling
Undersøgelsestype
Undersøgelsestype
Tilmelding (Faktiske)
Tilmelding
Fase
Fase
- Fase 1
Kontakter og lokationer
Studiesteder
-
-
Beijing
-
Beijing, Beijing, Kina, 100032
- Peking Union Medical College Hospital
-
-
Deltagelseskriterier
Berettigelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
Inclusion Criteria:
- Aged ≥ 18 but ≤ 65, male and female;
- Medical histories, physical examinations, laboratory examinations and study-related examinations and tests of the subjects,the Investigator judges that they are healthy;
- Body weight: 50- 80 kg, inclusive; Body mass index: 18.0 -26.0 kg/m2, inclusive;
- Vital signs: Blood pressure (90 mmHg≤ systolic ≤140 mmHg, 50 mmHg≤ diastolic ≤90 mmHg), heart rate (50≤ heart rate ≤100 beats/min), body temperature < 37°C;
- Subjects (including their partners) agree to take highly effective contraceptive measures during the study, and they have no birth plan or sperm donation plan within 6 months after the end of the study;
- Subjects are aware of the risks of the study, and voluntarily participate in the clinical study and sign an informed consent form (ICF).
Exclusion Criteria:
- History of cardiovascular, respiratory, kidney, liver, metabolism, endocrine, gastrointestinal, blood, nerve, skin and mental illness, cancer or other major disease that in the judgment of the Investigator might put the subject as risk on this study;
- Past history of tuberculosis, history of contact with active tuberculosis, TB-SPOT test results exceeding the upper limit of 2 times or more, and recent infectious diseases;
- During the screening and baseline period, the white blood cell count and C-reactive protein test results are abnormal and have clinical significance, hemoglobin: male <120g/L or female <110g/L;
- Electrocardiogram (ECG) abnormalities and have clinical significance;
- Subjects who have an autoimmune disease or an immune deficiency disease, or a family history of an autoimmune disease or an immune deficiency disease;
- Subjects with clinically obvious allergic diseases;
- Positive screening test results for human immunodeficiency virus (HIV-1/HIV-2) antibodies, hepatitis B surface antigen (HBsAg) or hepatitis C antibody (HCV-Ab), treponema pallidum antibody;
- Participate in any drug or vaccine clinical trial as a subject within 3 months before screening or prepare to be vaccinated during the study period to 2 months after the end of the study;
- Have received any monoclonal antibody or biological agent treatment within the previous 3 months;
- Have taken drugs that may affect immune function within 6 months before screening or have taken prescription/over-the-counter drugs within the previous 14 days;
- Subjects who have donated either more than approximately 500 mL of blood within 3 months prior to screening or any plasma within 4 weeks prior to screening; Subjects who donated blood (>400 ml) within 3 months prior to screening, or plasma exchange within 4 weeks prior to screening;
- Drink more than 5 cups of coffee, tea or cola per day (150ml and above per cup);
- Subjects who test positive for alcohol or drugs during the screening;
- Subjects who smoke or smoke test results are positive;
- Subjects with poor compliance;
- Pregnant or lactating women;
- The investigator believes that there are any subjects who are not suitable to participate in this trial.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Firedobbelt
Antal våben
Våben og indgreb
Deltagergruppe / ArmDeltagergruppe / Arm |
Intervention / BehandlingIntervention / Behandling |
|---|---|
|
Eksperimentel: Cohort 0.3mg/kg
All participants (fasted) received either 0.3 mg/kg of BDB-001 as a single dose or dose-matched placebo.
|
Intravenous injection
Intravenøs injektion
|
|
Eksperimentel: Cohort 1mg/kg
All participants (fasted) received either 1 mg/kg of BDB-001 as a single dose or dose-matched placebo.
|
Intravenous injection
Intravenøs injektion
|
|
Eksperimentel: Cohort 3mg/kg
All participants (fasted) received either 3 mg/kg of BDB-001 as a single dose or dose-matched placebo.
|
Intravenous injection
Intravenøs injektion
|
|
Eksperimentel: Cohort 8mg/kg
All participants (fasted) received either 8 mg/kg of BDB-001 as a single dose or dose-matched placebo.
|
Intravenous injection
Intravenøs injektion
|
|
Eksperimentel: Cohort 16mg/kg
All participants (fasted) received either 16 mg/kg of BDB-001 as a single dose or dose-matched placebo.
|
Intravenous injection
Intravenøs injektion
|
|
Eksperimentel: Cohort 20mg/kg
All participants (fasted) received either 20 mg/kg of BDB-001 as a single dose or dose-matched placebo.
|
Intravenous injection
Intravenøs injektion
|
Hvad måler undersøgelsen?
Primære resultatmål
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Incidence of Adverse Events, Clinically Significant Laboratory Abnormalities, Clinically Significant Electrocardiogram Abnormalities, Clinically Significant Vital Signs Abnormalities And Clinically Significant Physical Examination Abnormalities
Tidsramme: Up to 50 days
|
Up to 50 days
|
|
Maximum plasma concentration (Cmax)
Tidsramme: Up to 1200 hours postdose
|
Up to 1200 hours postdose
|
|
Area under the plasma concentration-time curve from time 0 to infinity (AUC0inf)
Tidsramme: Up to 1200 hours postdose
|
Up to 1200 hours postdose
|
|
Area under the plasma concentration-time curve from time 0 to 1200hr(AUC00-1200hr)
Tidsramme: Up to 1200 hours postdose
|
Up to 1200 hours postdose
|
|
Time of maximum concentration (Tmax)
Tidsramme: Up to 1200 hours postdose
|
Up to 1200 hours postdose
|
|
Elimination half-life (t1/2)
Tidsramme: Up to 1200 hours postdose
|
Up to 1200 hours postdose
|
|
Clearance (CL)
Tidsramme: Up to 1200 hours postdose
|
Up to 1200 hours postdose
|
|
Apparent volume of distribution (Vz)
Tidsramme: Up to 1200 hours postdose
|
Up to 1200 hours postdose
|
|
Mean residence time (MRT)
Tidsramme: Up to 1200 hours postdose
|
Up to 1200 hours postdose
|
Sekundære resultatmål
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Number of participants developing anti-BDB-001 antibodies
Tidsramme: Up to 50 days
|
Up to 50 days
|
Samarbejdspartnere og efterforskere
Sponsor
Sponsor
Samarbejdspartnere
Samarbejdspartnere
Datoer for undersøgelser
Studer store datoer
Studiestart (Faktiske)
Studiestart
Primær færdiggørelse (Faktiske)
Primær færdiggørelse
Studieafslutning (Faktiske)
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
Andre undersøgelses-id-numre
Andre undersøgelses-id-numre
- STS-BDB001-01
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
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 .