A Phase 1 Single Dose Study to Assess the Pharmacokinetics and Safety of the Biosimilar Ustekinumab Healthy Volunteers
- Conditions
- Plaque PsoriasisInflammatory and Immune System - Autoimmune diseasesSkin - Other skin conditions
- Registration Number
- ACTRN12619001473156
- Lead Sponsor
- euClone Proprietary Limited
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 210
1) Male or female, light smoker or non-smoker, greater than or equal to 18 and less than or equal to 55 years of age, with BMI greater than or equal to 17.0 and less than or equal to 32.0 kg/m2 and body weight greater than or equal to 50.0 kg and less than or equal to 100 kg.
2) Healthy as defined by:
a) the absence of clinically significant illness and surgery within 4 weeks prior to drug
administration.
b) the absence of clinically significant history of neurological (including seizures),
endocrine, cardiovascular (including unstable angina, heart failure, and myocardial
infarction), pulmonary (including chronic obstructive pulmonary disease [COPD]),
hematological, immunological, psychiatric, gastrointestinal, renal, hepatic,
dermatological (including eczema and allergic dermatitis), and metabolic diseases.
c) the absence of clinically significant active or chronic infection.
d) values for hematology and for biochemistry tests of blood and urine within the reference
ranges or showing no clinically relevant deviations as judged by the Investigator.
3) Females of childbearing potential who are sexually active with a non-sterile male partner
must be willing to use one of the following acceptable contraceptive methods throughout the study and for at least 105 days after drug administration
4) Females of non-childbearing potential defined as post-menopausal and surgically sterile
5) Male subjects who are not vasectomized for at least 6 months, and who are sexually active
with a female partner of childbearing potential must be willing to use one of
the following acceptable contraceptive methods throughout the study until at least 105 days
after drug administration
6) Male subjects with a pregnant partner must agree to use a condom throughout the study until at least 105 days after drug administration.
7) Male subjects must be willing not to donate sperm throughout the study until at least
105 days following drug administration.
8) Capable of consenting and complying with study requirements and procedures.
1) Any clinically significant abnormality at physical examination or clinically significant
abnormal laboratory test results at screening or Day -1.
2) Positive test for HIV, hepatitis B, or hepatitis C found during medical screening.
3) Positive pregnancy test at screening or Day -1.
4) History of allergic reactions to ustekinumab or other related drugs, or to any excipient in the
formulation.
5) History of previous exposure to ustekinumab or other anti-IL12/23 molecules for a medical
condition or in the context of another clinical research study.
6) Clinically significant 12-lead ECG abnormalities or vital sign abnormalities at screening.
7) History of significant drug abuse within 1 year prior to screening or positive urine drug
screen
8) History of significant alcohol abuse within 1 year prior to screening or regular use of alcohol
within 6 months prior to the screening visit
9) Participation in a clinical research study involving the administration of an investigational or
marketed drug or device within 30 days or 5 half-lives of the previous drug
10)Use of medications for the timeframes specified below, with the exception of medications
exempted by the Investigator on a case-by-case basis because they are judged unlikely to
affect the PK profile of the study drug or subject safety (e.g., topical drug products without
significant systemic absorption) and hormonal contraceptives
11)Have received a live attenuated vaccine within 1 month prior to screening or plan to receive
such vaccination during the study.
12)Donation of plasma within 7 days prior to dosing. Donation or loss of blood of 50 mL to 499 mL of blood within 30 days, or more than 499 mL within 56 days prior to drug administration.
13) Breast-feeding subject.
14)History of cancer, including any form of skin cancer, or strong family history of cancer
15)History of relevant anaphylactic reactions, drug, or food allergies.
16) Self or any first degree relative history with known disturbance of coagulation or blood disorder which would be cause for anemia or excess bleeding Inclusion of subjects with first degree relative history of thalassemia will be at the discretion of the
Investigator.
17)Any confirmed or suspected immunosuppressive or immunodeficient condition based on
medical history, family history, and physical examination.
18)History of clinically significant opportunistic infection
19)History of serious local infection or systemic infection within 3 months prior to screening.
20)History of recurrent infections, including recurring sinus and respiratory infections.
21) Presence of fever within 2 weeks prior to drug administration.
22)History of active tuberculosis or presence of active or latent tuberculosis, or positive
QuantiFERON®-TB test indicating possible tuberculosis infection.
23)Have resided or travelled in regions where tuberculosis or mycosis is endemic within
1 month prior to screening, or plan to visit such a region during the study.
24)Any reason which, in the opinion of the Investigator, would prevent the subject from
participating in the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To evaluate the PK similarity of Neulara with Stelara-EU and Stelara-US reference products following single SC injection of 45 mg/0.5 ml in healthy volunteers[Total 16 blood samples will be collected to assess PK similarity at: Pre-dose and 12, 24, 48 (Day 3), 72 (Day 4), 96 (Day 5), 144 (Day 7), 192 (Day 9), 240 (Day 11), 312 (Day 14),<br>480 (Day 21), 648 (Day 28), 984 (Day 42), 1488 (Day 63), 1992 (Day 84), and<br>2496 (Day 105) hours post-dose. PK parameters for all the blood samples will be calculated by standard non-compartmental method for AUC, Cmax, Tmax , T1/2, CL/F (total clearance)]
- Secondary Outcome Measures
Name Time Method