Last updated: January 27, 2022
Sponsor: University of Erlangen-Nürnberg Medical School
Overall Status: Active - Not Recruiting
Phase
4
Condition
Psoriatic Arthritis
Psoriasis And Psoriatic Disorders
Arthritis And Arthritic Pain
Treatment
N/AClinical Study ID
NCT04887597
EBIO
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
The trial population consists of patients of both sexes, aged ≥ 18 years, with activepsoriatic arthritis and an indication for systemic treatment. Patient eligible for study participation will have to fulfil the following requirements:
- Must be male or female and aged > 18 years at time of consent
- Clinical signs of enthesitis for at least 6 weeks prior to enrolment
- Indication for systemic treatment for PsA according to guidelines
- Patients who failed to respond to or who have a contraindication to, or are intolerantto other systemic therapy including cyclosporine or methotrexate
- bDMARD and tsDMARD naive
- Must understand and voluntarily sign an informed consent form including writtenconsent for data protection
- Must be able to adhere to the study visit schedule and other protocol requirements
- Male subjects (including those who have had a vasectomy) must agree to use barriercontraception (latex condoms) when engaging in reproductive sexual activity withFemales of Childbearing Potential (FCBP) while on study medication and for at least 28days after taking the last dose of study medication.
- Females of childbearing potential (FCBP) must have a negative urine pregnancy test atscreening and must be willing to use one effective form of birth control when engagingin reproductive sexual activity while on study medication and for at least 28 daysafter taking the last dose of study medication. Effective contraception methods include:
- Total abstinence (when this is in line with the preferred and usual lifestyle of thepatient. Periodic abstinence (e.g., calendar, ovulation, symptothermal, postovulationmethods) and withdrawal are not acceptable methods of contraception;
- Female sterilization (have had surgical bilateral oophorectomy with or withouthysterectomy);
- total hysterectomy or tubal ligation at least six weeks before taking investigationaldrug. In case of oophorectomy alone, only when the reproductive status of the womanhas been confirmed by follow up hormone level assessment;
- Male sterilization (at least 6 months prior to screening). For female patients on thestudy, the vasectomized male partner should be the sole partner of that Patient;
- Barrier methods of contraception: Condom or occlusive cap (diaphragm or cervical/vaultcaps)
- Use of oral, (estrogen and progesterone), injected or implanted hormonal methods ofcontraception or other forms of hormonal contraception that have comparable efficacy (failure rate <1 percent), for example hormone vaginal ring or transdermal hormonecontraception or placement of an intrauterine device (IUD) or intrauterine system (IUS); In case of use of oral contraception, women should have been stable on the samepill for a minimum of 3 months before taking investigational drug; In case localregulations deviate from the methods listed, local regulations apply and will bedescribed in the ICF; Women are considered post-menopausal and not of child bearingpotential if they have had at least 12 months of natural (spontaneous) amenorrhea withan appropriate clinical profile (e.g. age appropriate, history of vasomotor symptoms)or have had surgical bilateral oophorectomy (with or without hysterectomy), totalhysterectomy or tubal ligation at least six weeks ago. Additional eligibility criterium prior to enthesial biopsy:
- Presence of inflammation (enthesitis, synovitis, tendinitis, osteitis or tenosynovitis)in MRI or ultrasound examination of the elbow/ankle must be detectable
Exclusion
Exclusion criteria:
- Any contraindications for the treatment with secukinumab
- Subjects requiring systemic anticoagulation therapy or suffering from coagulationdisorders or any other condition which might interfere with enthesitis tissue sampling
- IBD (e.g. Crohn´s disease, ulcerative colitis)
- Investigational study drug within 4 weeks (or 5 half-lives, whichever is longer) priorto enrolment
- Patients taking high-potency opioid analgesics, including but not limited to,methadone, hydromorphone, and morphine
- Any contraindication or unwillingness to perform MRI
- Rheumatologic, inflammatory diseases, including but not limited to: AS, RA
- Pregnant or nursing (lactating) women, where pregnancy is defined as the state of afemale after conception and until the termination of gestation, confirmed by apositive human chorionic gonadotropin (hCG) laboratory test.
- Women of childbearing potential, defined as all women physiologically capable ofbecoming pregnant, unless they are using effective methods of contraception
- Any underlying metabolic, hematologic, renal, hepatic, pulmonary, neurologic,psychiatric, endocrine, cardiac, infectious or gastrointestinal conditions which inthe opinion of the investigator immune-compromises the patient and/or places thepatient at unacceptable risk for participation in a secukinumab therapy
- Active systemic infections during the last two weeks (exception: common cold) prior toenrolment.
- Evidence of tuberculosis infection as defined by either a positive purified proteinderivative (PPD) skin test (the size of induration will be measured after 48-72 hours,and a positive result is defined as an induration of ≥ 5mm or according to localpractice/guidelines), or a positive Quantiferon test. Patients with a positive testmay participate in the study if further work up (according to localpractice/guidelines) establishes conclusively that the patient has no evidence ofactive tuberculosis. If presence of latent tuberculosis is established then treatmentaccording to local country guidelines must have been initiated prior to enrolment.
- Infection with human immunodeficiency virus (HIV) Hepatitis B (HBV) or Hepatitis C (HCV)
- History of lymphoproliferative disease or any known malignancy or history ofmalignancy of any organ system (except for basal cell carcinoma or actinic keratosesthat have been treated with no evidence of recurrence in the past 3 months, carcinomain situ of the cervix or non-invasive malignant colon polyps that have been removed),treated or untreated within the past 5 years prior to enrolment.
- History or evidence of ongoing alcohol or drug abuse, within the last six months priorto enrolment.
- Planned administration of live vaccines during the study period or within 6 weeksprior to enrolment.
- Patients who possibly are dependent on the Sponsor, the Principal Investigator orInvestigator (e.g. family members).
Study Design
Total Participants: 10
Study Start date:
March 18, 2019
Estimated Completion Date:
September 30, 2022
Study Description
Connect with a study center
University Hospital Erlangen, Department of Internal Medicine 3, Rheumatology and Immunology
Erlangen, Bavaria 91054
GermanySite Not Available
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