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Trial details imported from ClinicalTrials.gov

For full trial details, please see the original record at https://clinicaltrials.gov/study/NCT05635084




Registration number
NCT05635084
Ethics application status
Date submitted
20/10/2022
Date registered
2/12/2022

Titles & IDs
Public title
A First-in-human Study of YN001 in Healthy Volunteers
Scientific title
A First-in-human, Randomized, Double-Blind, Placebo-Controlled, Single Ascending Dose and Multiple Ascending Dose Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Intravenously Administered YN001 in Healthy Subjects
Secondary ID [1] 0 0
YN001-001
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Cardiovascular Diseases 0 0
Condition category
Condition code

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Treatment: Drugs - YN001
Treatment: Drugs - Placebo for YN001

Experimental: YN001 - YN001 (with a strength of 5 mL:10 mg). Subjects will be administered 250 to 500 mL of YN001 diluted in 5% dextrose injection up to 120 min(which allows a +/-5 min infusion window) intravenous infusion.

Placebo comparator: Matching placebo for YN001 - Matching placebo for YN001 is 5% dextrose injection. Subjects will be administered 250 to 500mL of 5% dextrose injection up to 120 min (which allows a +/-5 min infusion window) intravenous infusion.


Treatment: Drugs: YN001
Dose ranges from 2-90mg

Treatment: Drugs: Placebo for YN001
5% dextrose injection to mimic the YN001
Intervention code [1] 0 0
Treatment: Drugs
Comparator / control treatment
Control group

Outcomes
Primary outcome [1] 0 0
The safety and tolerability of intravenously administered YN001 in healthy subjects.
Timepoint [1] 0 0
Up to 15 days of last dose
Secondary outcome [1] 0 0
Area under the plasma concentration-time curve from time 0 to the collection time point of the last measurable concentration (AUC0-t)
Timepoint [1] 0 0
Up to 168 hours of post initiation of last dose
Secondary outcome [2] 0 0
Area under the plasma concentration-time curve to infinity(AUCinf)
Timepoint [2] 0 0
Up to 168 hours of post initiation of last dose
Secondary outcome [3] 0 0
Maximum plasma concentration(Cmax)
Timepoint [3] 0 0
Up to 168 hours of post initiation of last dose
Secondary outcome [4] 0 0
Time of maximum concentration (Tmax)
Timepoint [4] 0 0
Up to 168 hours of post initiation of last dose
Secondary outcome [5] 0 0
Clearance(CL)
Timepoint [5] 0 0
Up to 168 hours of post initiation of last dose
Secondary outcome [6] 0 0
Elimination half-life (t1/2)
Timepoint [6] 0 0
Up to 168 hours of post initiation of last dose
Secondary outcome [7] 0 0
Volume of distribution estimates (Vdss)
Timepoint [7] 0 0
Up to 168 hours of post initiation of last dose
Secondary outcome [8] 0 0
Immunogenicity
Timepoint [8] 0 0
Up to 168 hours of post initiation of last dose

Eligibility
Key inclusion criteria
1. Written informed consent must be obtained before any assessment is performed.
2. Healthy male and female adults aged from 18 to 55 Years of age included, and in good health as determined by past medical history, physical examination, and vital signs, electrocardiogram, and laboratory tests at screening.
3. At screening, and baseline, vital signs (systolic and diastolic blood pressure and pulse rate) will be assessed in the sitting position after the subject has rested for at least three (3) minutes.
4. Weigh at least 50 kg, and have a body mass index (BMI) within the rage of 18-32 kg/m2.
5. Willing and able to comply with the requirements of the study.
Minimum age
18 Years
Maximum age
55 Years
Sex
Both males and females
Can healthy volunteers participate?
Yes
Key exclusion criteria
Subjects fulfilling any of the following criteria are not eligible for inclusion in this study.

1. Receiving an investigational agent at the time of enrollment, or within 30 days or 5 half-lifes of enrollment, whichever is longer prior to study drug administration.
2. Use of any prescription drugs, herbal supplements, within four (4) weeks prior to initial dosing, and/or over-the-counter (OTC) medication, COVID-19 vaccine, dietary supplements (vitamins included) within two (2) weeks prior to initial dosing. If needed, (i.e., an incidental and limited need of maximum 2 g per day, no more than 3 consecutive days within 2 weeks prior to dosing) paracetamol is acceptable, but must be documented in the Concomitant medications page of the CRF.
3. Fasting triglyceride concentration >2.8 mmol/L.
4. A history of clinically significant ECG abnormalities, or any of the following ECG abnormalities at Screening or Baseline:

* PR > 220 msec
* QRS complex > 120 msec
* QTcB > 450 msec (males)
* QTcB > 470 msec (females)
5. Pregnant or nursing (lactating) women.
6. Women of childbearing potential, defined as all women physiologically capable of becoming pregnant UNLESS the subject agrees to comply with highly effective, double barrier contraception for the entire duration of the study and for a period of 30 days after the dose of study drug. Fertile males, defined as all males physiologically capable of conceiving offspring UNLESS the subject agrees to comply with highly effective, double barrier contraception for the entire duration of the study and for a period of 30 days after the dose of study drug.
7. Smokers (use of tobacco products in the previous 1 month). Urine cotinine levels will be measured during screening and at baseline for all subjects. Smokers will be defined as any subject who reports tobacco use and/or who has a urine cotinine = 500 ng/mL. For light smokers to pass the cotinine test, smoking should be stopped at least 24 hours prior to reporting to the center (i.e., Day -2, early morning). Smoking will not be allowed during the study.
8. History of drug or alcohol abuse within the 12 months prior to dosing, or evidence of such abuse as indicated by the laboratory assays for alcohol, amphetamines, barbiturates, benzodiazepines, cannabinoids, cocaine, and opiates conducted during screening and/or baseline. Any THC-containing products should not be used at least 7 days prior to screening, and participant needs to abstain any THC-containing products during the trial. Alcohol abuse was defined as consumption of 14 or more standard drinks per week.
9. A positive hepatitis B surface antigen (HBsAg), or positive hepatitis C virus (HCV) or human immunodeficiency virus (HIV) test result.
10. A positive COVID-19 test result.
11. History of myopathy/myalgia, or susceptible to myopathy/rhabdomyolysis (e.g., hypothyroidism, family history of hereditary myopathy, previous muscle toxicity with HMG-CoA reductase inhibitors or fibrates).
12. Multiple drug allergies, or history of allergic reactions to rosuvastatin or any components of the study drug.
13. Donation or loss of more than 400 mL of blood within 3 months prior to study drug administration.
14. Plasma donation (> 100 ml) within 60 days prior to first dosing.
15. Hemoglobin levels below 12.0 g/dl at screening.
16. Recent (within the last 3 years) and/or recurrent history of autonomic dysfunction (e.g., recurrent episodes of fainting, palpitations, etc.).
17. Recent (within the last 3 years) and/or recurrent history of acute or chronic bronchospastic disease (including asthma and chronic obstructive pulmonary disease, treated or not treated), or cardiac dysfunction or myocardial infarction.
18. History of significant food allergies (e.g. anaphylactic reactions). Mild (non-anaphylactic, hypersensitivity) food allergies such as lactose intolerance/glucose intolerance are permitted.
19. Any surgical or medical condition which might significantly alter the distribution, metabolism, or excretion of drugs, or which may jeopardize the subject in case of participation in the study. The Investigator should make this determination in consideration of the subject's medical history and/or clinical or laboratory evidence of any of the following:

* Inflammatory bowel disease, ulcers, gastrointestinal or rectal bleeding in the last 6 months;
* Pancreatic injury or pancreatitis in the last 6 months;
* Liver disease or liver injury as indicated by abnormal liver function tests such as SGOT (AST), SGPT (ALT), ?-GT, alkaline phosphatase, or serum bilirubin. The Investigator should be guided by the following criteria:
* Any single parameter of ALT, AST, ?-GT, alkaline phosphatase, or serum bilirubin must not exceed 1.5 x upper limit of normal (ULN).
* Any elevation above ULN of more than one parameter of ALT, AST, ?-GT, alkaline phosphatase, or serum bilirubin excludes a subject from participation in the study.

If necessary, laboratory testing may be repeated on one occasion (as soon as possible) prior to randomization, to rule out any laboratory error.
* History or presence of impaired renal function as indicated by clinically significantly abnormal creatinine or BUN and/or urea values, or abnormal urinary constituents (e.g., albuminuria).
* Evidence of urinary obstruction or difficulty in voiding at screening.
20. Significant illness resolved within two (2) weeks prior to initial dosing.

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?
The people receiving the treatment/s

The people assessing the outcomes
The people analysing the results/data
Intervention assignment
Parallel
Other design features
Phase
Phase 1
Type of endpoint/s
Statistical methods / analysis

Recruitment
Recruitment status
Recruiting
Data analysis
Reason for early stopping/withdrawal
Other reasons
Date of first participant enrolment
Anticipated
Actual
16/12/2022
Date of last participant enrolment
Anticipated
Actual
Date of last data collection
Anticipated
29/08/2024
Actual
Sample size
Target
89
Accrual to date
Final
Recruitment in Australia
Recruitment state(s)
VIC
Recruitment hospital [1] 0 0
Nucleus Network Pty Ltd - Melbourne
Recruitment postcode(s) [1] 0 0
3004 - Melbourne

Funding & Sponsors
Primary sponsor type
Commercial sector/industry
Name
Beijing Inno Medicine Co., Ltd.
Address
Country

Ethics approval
Ethics application status

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 0 0
Ofer Gonen, Ph.D
Address 0 0
Nucleus Network Pty Ltd.
Country 0 0
Phone 0 0
Fax 0 0
Email 0 0
Contact person for public queries
Name 0 0
Jamie Zhang, Master
Address 0 0
Country 0 0
Phone 0 0
01082599080
Fax 0 0
Email 0 0
[email protected]
Contact person for scientific queries

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
No/undecided IPD sharing reason/comment


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

No documents have been uploaded by study researchers.


Results not provided in https://clinicaltrials.gov/study/NCT05635084