| Eligibility |
Inclusion Criteria:
1. Patient has signed the informed consent form (ICF) and documentation as required by
relevant competent authorities and is able to understand and adhere to the visit
schedule and study requirements.
2. Chinese patients shall be recruited in Mainland China.
3. Patient is male or female, aged 18 to 75 years old, inclusive, at time of Screening.
4. Patient weighs =100 kg at Screening and at BL.
5. Patient has had moderate to severe chronic PsO for at least 6 months.
6. Patient has involved body surface area (BSA) =10%, PASI =12, and sPGA =3 (moderate) at
Screening and at BL.
7. Patient has had stable psoriatic disease for at least 2 months (ie, without
significant changes as defined by the investigator or designee) prior to Screening.
8. Patient is a candidate for systemic therapy because the patient has had a previous
failure, inadequate response, intolerance, or contraindication to at least 1 systemic
antipsoriatic therapy including, but not limited to, methotrexate, cyclosporine,
psoralen plus ultraviolet light A (PUVA), and ultraviolet light B (UVB).
9. Patient has a negative QuantiFERON test for tuberculosis (TB) during Screening.
Note: Patients with an indeterminate QuantiFERON test are allowed if they have all of
the following:
1. No evidence of active TB on chest radiograph within 3 months prior to the first
dose of study drug.
2. Documented history of adequate prophylaxis initiation prior to receiving study
drug in accordance with local recommendations.
3. No known exposure to active TB after most recent prophylaxis.
4. Asymptomatic at Screening and BL. Investigators should check with the medical
monitor before enrolling such patients.
10. Patient is naïve to ustekinumab therapy, approved or investigational.
11. Women of childbearing potential (except those who are postmenopausal for more than 2
years or if surgically sterile) must have a negative serum pregnancy test during
Screening and negative urine pregnancy test at BL.
Sexually active women of childbearing potential must agree to use highly effective
contraception (sterilization, hormonal contraception pills or injection or implants, and
abstinence) for the duration of the study and until 4 months after the last dose of the
study drug. Male patients must agree to use contraception for the duration of the study and
agree not to donate sperm during and for 4 months after the last dose of study drug.
Note: Male partners of female subjects should also use contraception and should not donate
sperm until 4 months after the last dose of study drug.
Exclusion Criteria:
1. Patient diagnosed with psoriatic arthritis, erythrodermic psoriasis, pustular
psoriasis, guttate psoriasis, medication-induced psoriasis, other skin conditions (eg,
eczema), or other systemic autoimmune disorder inflammatory disease at the time of the
Screening Visit that would interfere with evaluations of the effect of the study drug
on psoriasis.
2. Patient has prior use of any of the following medications within specified time
periods or will require use during the study:
1. Topical medications within 2 weeks of BL visit (except low- to mid-potency
topical corticosteroids on face, eyes, scalp, palms, soles, and genital area;
only).
2. PUVA phototherapy and/or UVB phototherapy within 4 weeks prior to the BL visit.
3. Nonbiologic psoriasis systemic therapies (eg, cyclosporine, methotrexate, and
acitretin) within 4 weeks prior to the BL visit.
4. Any systemic steroid in the 4 weeks prior to the BL visit.
5. Any oral traditional Chinese medicine (TCM) 4 weeks prior to the BL visit or any
topical TCM 2 weeks prior to the BL visit.
6. Investigational agent(s) within 90 days or 5 half-lives (whichever is longer)
before BL visit.
7. Other systemic biologics within 90 days or 5 half-lives (whichever is the longer)
before BL visit.
8. Any therapeutic agent targeting IL-12, IL-17 or IL-23 at any time. Specified
washout periods for approved/marketed products are provided in Table 5.1.
Table 5.1: Approved/Marketed Products Medication or Therapy Washout before BL Biologic
Therapies, including but limited to: Adalimumab Etanercept Secukinumab Infliximab
Certolizumab pegol Alefacept Briakinumab Guselkumab Brodalumab 12 weeks 8 weeks 12
weeks 12 weeks 24 weeks 24 weeks 24 weeks 13 weeks 13 weeks Any kinase inhibitor for
any reason (eg, tofacitinib citrate) 1 day Any phosphodiesterase type 4 inhibitor (eg,
apremilast [Otezla]) 4 weeks Cyclosporine 4 weeks Methotrexate 4 weeks PUVA-UVA/UVB 4
weeks Topical psoriasis treatments (examples include vitamin D analogs, topical
steroids, polifenols, etc) (except low- to mid-potency topical corticosteroids on
face, eyes, scalp, palms, soles, and genital area; only) 2 weeks Oral retinoids 4
weeks Corticosteroids IM - IV - oral - intraarticular 4 weeks Drugs that may cause new
onset or exacerbation of psoriasis (including, but not limited to, beta blockers,
lithium, and anti-malarials) 6 months1 TCM (oral) TCM (topical) 4 weeks 2 weeks
Abbreviations: BL = Baseline; IM = intramuscular; IV = intravenous; PUVA = psoralen
plus ultraviolet light A; TCM = traditional Chinese medicine; UVA = ultraviolet light
A; UVB = ultraviolet light B. 1 Unless the patient has been on a stable dose for at
least 6 months prior to BL Visit without exacerbation of psoriasis.
3. Patient has received live or attenuated vaccines during the 4 weeks prior to BL visit
or has the intention of receiving a live or attenuated vaccine at any time during the
study.
Note: Inactivated (non-live and non-attenuated) vaccines are allowed.
4. Patient has an underlying condition (including, but not limited to metabolic,
hematologic, renal, hepatic, pulmonary, neurologic, endocrine, cardiac, infectious, or
gastrointestinal) which, in the opinion of the investigator or designee, significantly
immunocompromises the patient and/or places the patient at unacceptable risk for
receiving an immunomodulatory therapy.
5. Patient has a planned surgical intervention during the duration of the study except
those related to the underlying disease and which, in the opinion of the investigator
or designee, will not put the patient at further risk or hinder the patient's ability
to maintain compliance with study drug and the visit schedule.
6. Patient has an active and serious infection or history of infections as follows:
a. Any active infection (including Severe Acute Respiratory Syndrome-Coronavirus-2
[SARS-CoV-2] infection) i. For which non-systemic anti-infectives were used within 4
weeks prior to BL visit. Note: patients receiving topical antibiotics for facial acne
do not need to be excluded.
ii. Which required hospitalization/quarantine or systemic anti-infective within 8
weeks prior to BL visit.
b. Recurrent or chronic infections or other active infection that, in the opinion of
the investigator or designee, might cause this study to be detrimental to the patient.
c. Invasive fungal infection or mycobacterial infection. d. Opportunistic infections,
such as listeriosis, legionellosis, or pneumocystis.
7. Patient is positive for human immunodeficiency virus (HIV), hepatitis C virus (HCV)
antibody, hepatitis B surface antigen (HBsAg), or hepatitis B core antibody (HBcAb).
8. Patient has severe progressive or uncontrolled, clinically significant disease that in
the judgment of the investigator or designee renders the patient unsuitable for the
study.
9. Patient has a history of malignancy within 5 years except for adequately treated
cutaneous squamous or basal cell carcinoma, in situ cervical cancer or in situ breast
ductal carcinoma.
10. Patient has active neurological disease such as multiple sclerosis, Guillain-Barré
syndrome, optic neuritis, transverse myelitis, or history of neurologic symptoms
suggestive of central nervous system demyelinating disease.
11. Patient has moderate to severe heart failure (New York Heart Association class
III/IV).
12. Patient has uncontrolled diabetes mellitus type 1 or 2.
13. Patient has a history of hypersensitivity to the active substance or to any of the
excipients of Stelara or AVT04.
14. Patient is pregnant or nursing (lactating) women, where pregnancy is defined as the
state of a female after conception and until the termination of gestation.
15. Patient has evidence (as assessed by the investigator or designee using good clinical
judgment) of alcohol or drug abuse or dependency at the time of Screening, for the 5
years prior to Screening, or during the study.
16. Patient is unable to follow study instructions and comply with the protocol in the
opinion of the investigator or designee.
17. Patient has a history of clinically significant hematological abnormalities, including
cytopenia (eg, thrombocytopenia, leukopenia).
18. Patient has a laboratory abnormality that, in the opinion of the investigator or
designee, could cause this study to be detrimental to the patient. The following
laboratory abnormalities should be excluded:
1. Hemoglobin <9 g/dL
2. Platelet count <100,000/mm³
3. White blood cell count <3000 cells/mm³
4. Aspartate aminotransferase and/or alanine aminotransferase that is persistently
=2 × the upper limit of normal. (Persistently indicates at least on 2 occasions
separated by a number of days, per the rescreening procedure)
5. Creatinine clearance <50 mL/min (Cockcroft-Gault formula)
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