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About
The main objective of this study is to investigate the safety and tolerability of si-544.
Other objectives are to study the metabolism of si-544 in the body and to assess the effects of si-544 on cells of the body's immune system (immune cells) that have been chronically activated by the disease. Likewise, the effect of si-544 on inflammatory responses in the body triggered by the disease and other disease symptoms will be investigated.
Enrollment
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Volunteers
Inclusion criteria
Subject has the capacity for consenting, was informed about the nature, the scope, and the relevance of the clinical study, voluntarily agrees in participation and in the study provisions, and duly signed the ICF approved by the ethics committee before any study-related procedure is performed
Men and women aged ≥18 to 75 years
Willing and able to adhere to the protocol requirements
Women of childbearing potential must:
Reliable methods for this study are:
i. combined (estrogen and progestogen containing) hormonal contraception associated with inhibition of ovulation (oral, intravaginal, transdermal) ii. progestogen-only hormonal contraception associated with inhibition of ovulation (oral, injectable, implantable) iii. intrauterine device iv. intrauterine hormone-releasing system v. bilateral tubal occlusion vi. vasectomized sexual partner (provided that the partner is the sole sexual partner of the woman of childbearing potential and has received medical assessment of the surgical success) vii. sexual abstinence (only if defined as refraining from heterosexual intercourse during the entire period of risk associated with the study treatment) Abstinence is only accepted as true abstinence: when this is in line with the preferred and usual lifestyle of the subject (periodic abstinence [eg, calendar, ovulation, symptothermal, postovulation methods and withdrawal] is not an acceptable method of contraception).
c. agree to abstain from breast feeding during the study participation and for 90 days after the last IMP injection
Postmenopausal (no menses for at least 1 year without alternative medical cause) or surgically sterile women (tubal ligation, hysterectomy, or bilateral oophorectomy)
Men must agree to practice true abstinence or to use a condom during sexual contact with a pregnant woman or a woman of childbearing potential during study participation and for at least 90 days after the last IMP injection, even after undergoing a successful vasectomy.
Ps-specific inclusion criteria:
Diagnosis of Ps at least 3 months before Screening
Active Ps with ≥3% BSA involved and with at least 1 psoriatic plaque (other than nail change)
PsA-specific inclusion criteria:
Diagnosis of PsA based on the classification for psoriatic arthritis criteria (CASPAR) at least 3 months before Screening
Diagnosis of active Ps with at least 1 psoriatic plaque (other than nail change)
Active PsA defined as
≥1 tender joint out of 68 assessed joints, and
≥1 swollen joint out of 66 assessed joints (dactylitis of a digit counts as one joint each), and
negative results for rheumatoid factor and anti-cyclic citrullinated peptide antibodies
Exclusion criteria
Known history of hypersensitivity to constituents or excipients in the pharmaceutical formulation of the IMP
Uncontrolled hypertension or uncontrolled diabetes, as judged by the investigator
Chronic disease other than Ps or PsA not adequately controlled by stable treatment (ie, no changes or initiation of treatment within 4 weeks before Screening and Day 1)
History of seizures
Presence or history of paresthesia or neuropathy
Clinically significant ECG abnormalities, as judged by the investigator
Clinically relevant disease which could affect the safety of the subject during the study or impede the subject's ability to complete the study, as assessed by the investigator
Presence of acute infection within 7 days before Screening or Day 1, as judged by the investigator
Known or active infection with Mycobacterium tuberculosis and/or positive tuberculosis interferon γ release assay result at Screening
Known or active infection with HIV, hepatitis B virus, or hepatitis C virus
Known or suspected abuse of alcohol, drugs, or medicinal products
Therapy with biologics used for the treatment of Ps and/o PsA (including those under investigation) within 1 year before Day 1
UV phototherapy or systemic therapy (except methotrexate for the treatment of PsA) within 4 weeks of Day 1
Vaccination within 2 weeks (for live vaccines within 4 weeks) before Day 1 and/or planned vaccination during the treatment period
Current or previous (within 4 weeks before Day 1) participation in another clinical study with an IMP or a medical device
Employee of the sponsor, or employee, or relative of the investigator
Committed to an institution by virtue of an order issued either by the judicial or the administrative authorities
Legal incapacity or limited legal capacity
Ps-specific exclusion criteria:
Drug-induced psoriasis
PsA-specific exclusion criteria:
Primary purpose
Allocation
Interventional model
Masking
45 participants in 2 patient groups, including a placebo group
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Central trial contact
Andreas Klostermann, Dr.
Data sourced from clinicaltrials.gov
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