to evaluate pharmacokinetics, safety and tolerability of ZYBK2 in healthy adult human volunteers
- Registration Number
- CTRI/2020/08/027011
- Lead Sponsor
- Cadila Healthcare Ltd
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 31
1.Healthy male and female subjects between 18 and 55 years of age (Both inclusive).
2.Body mass index of 18.5 to 30.0 kg/m2 (Both inclusive) with a body weight of 50 to 100 kg (Both inclusive).
3.Normal QTc interval at screening and Check In [QTcF �450 ms]
4.Capable of giving written informed consent, which includes compliance with the study procedures, restrictions, and requirements listed in the protocol.
5.Subjects who, in the opinion of the Investigator, are healthy as determined by their pre study medical history, clinical examination, 12-lead ECG and clinical laboratory tests within the institutional normal range or judged as not clinically significant by the Investigator, including the following parameters: hematology, serum biochemistry, urinalysis, and serology
6.Male subjects and female subjects of childbearing potential must practice highly effective contraception
1.History or presence of alcoholism or drug abuse within the past 1 year.
2.Presence or history of any of the following disorders/disease within the past 3 months, that might have impact on the clinical trial as per the investigator discretion: cardiovascular, cerebrovascular, dermatological, gastrointestinal, gynecological, hematological, hepatic, malignancy, metabolic, musculoskeletal, neurological, psychiatric, renal, respiratory, venereal, any other major disorders
3.History of clinically significant hypersensitivity, intolerance, or allergies, as determined by the Investigator.
4.History or presence of smoking or consumption of tobacco/nicotine products within the past 1 year.
5.Difficulty with donating blood.
6.Systolic blood pressure more than 140 mmHg and less than 100 mmHg and diastolic blood pressure more than 90 mmHg and less than 60 mmHg.
7.Pulse rate less than 55/minute and more than 100/minute.
8.Any clinically significant laboratory or ECG findings during screening or check-In.
9.Surgery within last 3 months or planned major surgery within next 3 months from the date of screening (other than minor cosmetic surgery and minor dental surgery).
10.Subjects who have recent illness (eg, fever) within 7 days of check-in
11.Volunteers who have participated in any drug research study within past 3 months.
12.Volunteers who have donated one unit (350 ml) of blood in the past 3 months.
13.Has used prescription drugs and other substances (eg, dietary or herbal supplements such as St Johnââ?¬•s Wort) known to be either significant enzyme inducers or enzyme inhibitors within 4 weeks of Day 0, or use of grapefruit or similar substances (Seville oranges or marmalade, grapefruit juice, grapefruit hybrids, pomelos, exotic citrus fruits or fruit juices) within 7 days of Day 0.
14.Use of any over-the-counter (OTC), any prescription medications or alternative tradition of medicine (herbal medicines, homoeopathy, Siddha, Unani, etc.) within the 15 days or 5 half-lives (whichever is longer), prior to receiving study drug that might have impact on the clinical trial as per the investigator discretion.
15.A positive urine drugs of abuse test or positive alcohol breath test at check-in.
16.History of, or positive screening test for, hepatitis C infection (defined as positive for hepatitis C virus antibody), hepatitis B infection (defined as positive for hepatitis B surface antigen), or human immunodeficiency virus I or II.
17.Female subjects who are pregnant, currently breastfeeding, or attempting to conceive.
18.Any disorder that, in the Investigatorââ?¬•s opinion, may interfere with study compliance, such as significant mental, nervous disorder or other illness. In making this assessment, the Investigator must refer to the study information provided including the Investigatorââ?¬•s Brochure.
19.Inability to be venipunctured or tolerate venous puncture.
20.Any condition or abnormal baseline findings that in the Investigatorââ?¬•s judgment might increase the risk to the subject or decrease the chance of obtaining satisfactory data needed to obtain the objective of the study.
21.Other unspecified reasons that, in the opinion of the Investigator or the Sponsor, make the subject unsuitable for the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To characterize the pharmacokinetics of ZYBK2 when administered as a single subcutaneous dose to healthy subjectsTimepoint: Screening and Day 7
- Secondary Outcome Measures
Name Time Method �To evaluate safety and tolerability of ZYBK2 administered to healthy subjectsTimepoint: Screening and Day 7