Study of sonelokimab injection in adults with active psoriatic arthritis who have not received biological DMARDs treatment before

1 1

What is this study about?

This study focuses on psoriatic arthritis, a condition that causes joint pain and inflammation in people who have psoriasis. The study will test a new medication called sonelokimab, which is given as a subcutaneous injection under the skin. This medicine works by blocking specific proteins in the body that cause inflammation.

The purpose of this research is to determine how well sonelokimab works compared to placebo in treating people with active psoriatic arthritis who have not previously used biological medications. The study will compare two different ways of giving sonelokimab against placebo treatment.

Participants will receive either sonelokimab injections or placebo for 16 weeks. The medication dose will be 60 milligrams, given every four weeks. Throughout the study, doctors will monitor the participants’ symptoms, particularly focusing on how their joint pain and inflammation respond to the treatment. The study will also track any changes in participants’ ability to perform daily activities and their overall well-being.

1 Initial visit and assessment

You will undergo initial assessment to confirm your eligibility for the study if you have psoriatic arthritis for at least 6 months

Your doctor will verify that you have at least 3 tender joints and 3 swollen joints

You must have at least one psoriatic plaque of 2 cm or more, or nail changes consistent with psoriasis

2 Assignment to treatment group

You will be randomly assigned to one of three groups:

Group 1: Sonelokimab 60 mg with induction regimen

Group 2: Sonelokimab 60 mg without induction regimen

Group 3: Placebo (inactive substance)

3 Treatment administration

You will receive subcutaneous injections (under the skin)

The treatment will be given every 4 weeks

The study will continue for at least 16 weeks to evaluate the primary results

4 Monitoring and assessment

Regular evaluations will check your joint pain and swelling

Your psoriasis symptoms will be monitored

Blood tests and other safety assessments will be performed

Your ability to perform daily activities will be evaluated

X-rays will be taken to check joint damage

5 Final assessment

At week 16, your response to treatment will be evaluated

The main measurement will be a 50% improvement in arthritis symptoms (ACR50)

Your psoriasis improvement will be assessed if you had skin involvement at the start

Overall health status and quality of life measurements will be taken

Who Can Join the Study?

  • Must be at least 18 years old
  • Must have confirmed psoriatic arthritis with symptoms present for at least 6 months
  • Must have moderate to severe active disease with at least 3 tender joints and 3 swollen joints
  • Must have active plaque psoriasis with at least one psoriatic patch of 2 cm or larger, or nail changes from psoriasis, or documented history of plaque psoriasis
  • Must test negative for rheumatoid factor and anti-cyclic citrullinated peptide (proteins found in blood that can indicate certain types of arthritis)
  • Must have been taking stable doses of anti-inflammatory medications (NSAIDs) for at least 4 weeks with inadequate symptom control, or have documented inability to take these medications
  • Must have tried at least one conventional disease-modifying medication (such as methotrexate, sulfasalazine, or leflunomide) for at least 12 weeks with inadequate response, or have documented inability to take these medications
  • Must have at least one bone erosion on hand and feet X-rays OR elevated levels of C-reactive protein (a marker of inflammation in blood)
  • Women who can become pregnant must use effective birth control during the study and for 8 weeks after the last treatment
  • Men must use condoms when sexually active with partners who can become pregnant during the study and for 8 weeks after the last treatment, unless surgically sterile
  • Must be able to follow the study protocol and schedule
  • Must be able to understand and sign informed consent documents

Who Cannot Join the Study?

  • Age below 18 or above 75 years old
  • Previous treatment with sonelokimab (the study medication)
  • Known allergic reactions to biological medications
  • Active or chronic infections, including tuberculosis and hepatitis B or C
  • History of cancer within the past 5 years (except successfully treated non-melanoma skin cancer)
  • Pregnant or breastfeeding women
  • Significant heart problems or uncontrolled high blood pressure
  • Severe kidney or liver disease
  • Other inflammatory arthritis conditions besides psoriatic arthritis
  • Major surgery planned during the study period
  • Participation in another clinical trial within 30 days before this study
  • Active substance abuse or mental health conditions that could interfere with study participation
  • Use of prohibited medications, including certain immunosuppressive drugs (medications that weaken the immune system)
  • Unstable psoriatic arthritis requiring immediate change in treatment
  • Live vaccines received within 12 weeks before starting the study

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Site Name City Country Status
Futuremeds Sp. z o.o. Wroclaw Poland
Centrum Terapii Wspolczesnej J.M. Jasnorzewska S.K.A. Lodz Poland
CHU Grenoble Alpes La Tronche France
Reumedika s.c. Poznan Poland
NZOZ LECZNICA MAK-MED s.c. Nadarzyn Poland
Praxis für Rheumatologie, Gastroenterologie und Innere Medizin Munich Germany
CENTRUM MEDYCZNE REUMA PARK Warsaw Poland
Vasarhelyi Sarkanyfu Kft. Hodmezovasarhely Hungary
Acibadem City Clinic Diagnostic And Consultation Center Tokuda EAD Sofia Bulgaria
Unidade Local De Saúde De Santa Maria, E.P.E. Lisbon Portugal
Innomedica OÜ Tallin Estonia

Other Sites

Site Name City Country Status
Centre Hospitalier Universitaire Rouen Rouen France
Kistarcsai Flor Ferenc Korhaz Kistarcsa Hungary
Praglandia s.r.o. Prague Czechia
Diagnostic Consulting Center XVII Sofia Ltd. Sofia Bulgaria
Saint Maria Hospital Bucharest Romania
Spitalul Clinic Judetean De Urgenta Craiova Craiova Romania
Lukmed 2 Sp. z o.o. Siedlce Poland
Bekes Varmegyei Koezponti Korhaz Gyula Hungary
CCAB Centro Clinico Academico Braga Associacao Braga Portugal
University General Hospital Of Heraklion Heraklion Greece
Rcmed Oddzial Sochaczew Sochaczew Poland
Hospital Universitario Basurto Bilbao Spain
Reumed Sp. z o.o. Lublin Poland
Twoja Przychodnia Nowosolskie Centrum Medyczne Sp. z o.o. Nowa Sol Poland
Hospital Quironsalud Sagrado Corazon Sevilla Spain
Silmedic Sp. z o.o. Katowice Poland
University Multiprofile Hospital For Active Treatment Kaspela EOOD Plovdiv Bulgaria
Clinicmed Daniluk Nowak Sp. k. Bialystok Poland
Albamed s.r.o. Zvolen Slovakia
Qualiclinic Kft. Budapest Hungary
Malopolskie Badania Kliniczne Sp. z o.o. Cracow Poland
Medical Center Teodora EOOD Ruse Bulgaria
Instituto Portugues De Reumatologia Lisbon Portugal
MVZ Rheumatologie und Autoimmunmedizin Hamburg GmbH Hamburg Germany
Unidade Local De Saude Do Alto Minho E.P.E. Ponte De Lima Portugal
Centrum Medyczne Oporow Wroclaw Poland
Athens Naval Hospital Athens Greece
Meditsinski Tsentar-N.I Pirogov EOOD Sofia Bulgaria
Mbal Lyulin EAD Sofia Bulgaria
Medicinski centar Kuna Peric d.o.o. Zagreb Croatia
Revita Kft. Budapest Hungary
Medical Center Zara-Med EOOD Stara Zagora Bulgaria
Centre Hospitalier Jean Rougier Cahors France
Complex Rendelo Med Zrt. Szekesfehervar Hungary
Kaunas city polyclinic Public institution Kaunas Lithuania
Accellacare Espana S.L. Alcobendas Spain
Policlinica CCBR S.R.L. Bucharest Romania
Nova Reuma Domyslawska I Rusilowicz Lekarza Reumatologa I Fizjoterapeuty sp.p. Bialystok Poland
Dc-Med Michal Kowalski sp.k. Swidnica Poland
Ambulatorium Sp. z o.o. Elblag Poland
Ai Centrum Medyczne Sp. z o.o. Poznan Poland
Termedia Sp. z o.o. Poznan Poland
Malopolskie Centrum Kliniczne Cracow Poland
Rheuma Medicus Sp. z o.o. Warsaw Poland
Wromedica I Bielicka A Strzalkowska s.c. Wroclaw Poland
Etyka Osrodek Badan Klinicznych Tomasz Pesta S.K.A. Olsztyn Poland
Medman s.r.o. Martin Slovakia
Reumex s.r.o. Rimavska Sobota Slovakia
Artromac N.O. Kosice Slovakia
Rheumatologische Schwerpunktpraxis Berlin Germany
Obudai Egeszseguegyi Centrum Kft. Dunaújváros Hungary
Revmatologicky Ustav Prague Czechia
University Multiprofile Hospital For Active Treatment Saint Georgi EAD Plovdiv Bulgaria
Szpital Uniwersytecki Nr 2 Im Dr Jana Biziela W Bydgoszczy Bydgoszcz Poland
Clinica Gaias Santiago Santiago De Compostela Spain
Etg Neuroscience Sp. z o.o. Warsaw Poland
University Of Debrecen Debrecen Hungary
Hospital Clinico Universitario De Valencia Valencia Spain
Dkc Fokus-5 Lzip OOD Sofia Bulgaria
Med Polonia Sp. z o.o. Poznan Poland
Affidea Praha s.r.o. Prague Czechia
Rigas 1. slimnica SIA Riga Latvia
MUDR. Zuzana URBANOVA Prague Czechia
Centrum Kliniczno-Badawcze J.Brzezicki, B.Gornikiewicz-Brzezicka Lekarze Sp. p. Elblag Poland
Spitalul Judetean De Urgenta Sfantul Ioan Cel Nou Suceava Suceava Romania
Hospital Quirón Salud Infanta Luisa Sevilla Spain
Hospital Universitario Virgen Macarena Sevilla Spain
Respublikine Siauliu ligonine VšĮ Siauliai Lithuania
Clinique De L’infirmerie Protestante De Lyon Caluire Et Cuire France
Virgen del Rocío University Hospital Sevilla Spain
NIEPUBLICZNY ZAKŁAD OPIEKI ZDROWOTNEJ BIF-MED S.C. A. Wawiernia,M. Roykiewicz,R. Roykiewicz Bytom Poland
Medyczne Centrum Hetmanska Poznan Poland
Universitaetsklinikum Erlangen AöR Erlangen Germany
Centre Hospitalier Universitaire De Montpellier Montpellier France
Universidade De Santiago De Compostela Santiago De Compostela Spain
Hospital General Universitario De Valencia Valencia Spain
Szabolcs-Szatmar-Bereg Varmegyei Oktatokorhaz Nyiregyhaza Hungary
Hospital General Universitario De Castellon Castello De La Plana Spain
Centre Hospitalier Universitaire De Nice Nice France
University Multiprofile Hospital For Active Treatment Eurohospital Plovdiv Ltd. Plovdiv Bulgaria
Medical Center Artmed Ltd. Plovdiv Bulgaria
Somed Cr Sp. z o.o. sp.k. Lodz Poland
St. Elisabeth Gruppe GmbH Katholische Kliniken Rhein-Ruhr Herne Germany
MediTrials OÜ Tartu Estonia
Satucon Oy Kuopio Finland
Klaipedos universiteto ligonine VšĮ Klaipeda Lithuania
Staedtisches Klinikum Dresden Dresden Germany
PV-Medical s.r.o. Zlin Czechia
Twoja Przychodnia Poznańskie Centrum Medyczne Sp. z o.o. Poznan Poland
Fakultni Thomayerova nemocnice Prague Czechia
North Estonia Medical Centre Foundation Tallin Estonia
Medicover GmbH Oldenburg In Holstein Germany
REUMA CENTRUM Specjalistyczna Praktyka Lekarska Dr n. med. Jakub Trefler Warsaw Poland
Centre Hospitalier De Narbonne Narbonne France
Vital Medical Center Veszprem Hungary
Myqyxtkan Innfasurdl Cnyezaev Sjvsdkoa Slb z obfk Warsaw Poland
Fuqgfmterj Skpqe Spoe Madrid Spain
Tmmfofdgjxx uqq Slyaxicdfse Bbmxxpda Goty Bad Bentheim Germany
Rkucrmxqekiy slioya Brno-Sever Czechia
Lerpvwnp Srgk Lisbon Portugal
Rekere sefrzj Breclav Czechia
Ccypdw plfwwxeukih Vilnius Lithuania
Cnmbzqa Mkhfgi Cydtxuunq ds Suqli Tsxtok Sd – Hvzjdtlr Ltsbhbph Bjnqg Braga Portugal
Clefkaf Dvq Sswb Madrid Spain
Cksizki Dk Kmchcslbmdpnc Sw Mkmov Bmjpe Senmpx Timisoara Romania
Hdtmyrgb Srhq Bucharest Romania
Evy Lldeew Sdf z ouor Debica Poland
Cspvlej Mkiwqdct Jeagdmc Sjx z otpe Warsaw Poland
Ulnvm Co Sde z ofqh Dabrowka Poland
Rtcqglul Pdzugv smpqjx Poprad Slovakia
Qylobkz Mxpaawg Cgnkjv Srdelw Bucharest Romania
Vrebalew sltitg Moravska Ostrava A Privoz Czechia
Horwbppv Uvzsbalyzsfym Rzyuqlkn Df Mcbods Malaga Spain
Pmjg Txlhx Htpwjwdz Uzwtkurujsqs Sabadell Spain
Bkhjmawdts Irdmkquocakl Beirp Ilwvydidzfger Kkgrhm Budapest Hungary
Pgbglyb Mzytve Sfq z Ozup Epb Pncaesztg Poniatowa Poland
Sunpugje Cgfilt &ddizbekdr Iw Cdwlzmodvcmwyysjic Bucharest Romania
Mjaxqwjms Mtanako ggpxd Munich Germany
Mrxxjas Cucept Ekfknx Mjormn Oms Pleven Bulgaria
Kgqexxzf brgebdhj cakxvw Rzujhq (kqwikmvx Htpflohi Csbivi Rccrtkt Rijeka Croatia
Ppjrbwrl Ptwstbqc Lkijnhaj Peox De Hal Mps Pwroo Hcvsgt Poznan Poland
Eaa Zxxtup Zamosc Poland
Khns Spo z osqz Wołomin Poland
Kxtc Kolexycjw Vnanqfgs Jpzirlypizl Czestochowa Poland
Fyyubvpw nrreymiug Mvzrj a Hgpylvj Prague Czechia
Cqkogq Hdovgmtbxkp Roymnzuu Uvxbcrtmiykgq Dk Twfum Tours France
Ktrhrbtv dan Ukhkbrminpmb Mikfwggp Aov Munich Germany
Ivmnvagyhygczxvsokke Gakt Berlin Germany
Fzmywtdcd Pmux Ls Iyjarnovwgyoi Bwwxkrzah Dve Hmlzlthh Upwzdjiffbscf Lr Pvi Madrid Spain
Cagqsnhdw Srwlydui scmjlo Butovice Czechia
Imtjaund dq Cuhknkcinxoi Hvfohhyyiav Uguwucnkskgzl do Srzcs Ekqoroj (tqmxnvv Saint Priest En Jarez France
Hfqdefpt Uqnaewmgdmbqx di A Crguql A Coruna Galicia Spain
Uijkpfegry Goytone Hatlentl Auykcaq Athens Greece
M &pixn M coqzcs Slx Adazi Latvia
Jvffbb Bdu Kalocsa Hungary

Want to learn more about this study or check if you can participate? Contact us.

Trial status

Country Status Recruitment Start
Bulgaria Bulgaria
Not recruiting
02.05.2025
Croatia Croatia
Not recruiting
02.05.2025
Czechia Czechia
Not recruiting
02.05.2025
Estonia Estonia
Not recruiting
02.05.2025
Finland Finland
Not recruiting
02.05.2025
France France
Not recruiting
02.05.2025
Germany Germany
Not recruiting
02.05.2025
Greece Greece
Not recruiting
02.05.2025
Hungary Hungary
Not recruiting
02.05.2025
Latvia Latvia
Not recruiting
02.05.2025
Lithuania Lithuania
Not recruiting
02.05.2025
Poland Poland
Not recruiting
02.05.2025
Portugal Portugal
Not recruiting
02.05.2025
Romania Romania
Not recruiting
02.05.2025
Slovakia Slovakia
Not recruiting
02.05.2025
Spain Spain
Not recruiting
02.05.2025

Trial locations

Investigated drugs:

Sonelokimab is a new biological medication that is being studied for treating psoriatic arthritis. It is given as an injection under the skin (subcutaneously) to patients who have never received biological disease-modifying antirheumatic drugs (DMARDs) before. This medication works by targeting specific components of the immune system that are involved in causing joint inflammation and skin symptoms in psoriatic arthritis.

A Placebo is used in this study as a comparison treatment. It is an inactive substance that looks identical to the real medication but contains no active ingredients. This helps researchers determine how effective the actual medication is by comparing results between patients who receive the real medication and those who receive the placebo.

Psoriatic arthritis – A chronic inflammatory joint condition that typically develops in people who have psoriasis. The condition causes joint pain, stiffness, and swelling that can affect any part of the body, particularly the fingers, toes, wrists, ankles, and lower back. It often results in joints becoming tender and swollen, with some people experiencing reduced range of motion. The condition can vary in severity, with some people having mild symptoms while others experience more persistent joint problems. The inflammation can also affect surrounding tendons and ligaments, causing additional discomfort and reduced mobility.

Trial ID:
2024-516213-20-00
Protocol code:
M1095-PSA-301
Trial Phase:
Therapeutic confirmatory (Phase III)

Other Trials to Consider

  • Tulisokibart for Psoriatic Arthritis in Adults

    Recruiting

    Investigated drugs:
    Germany Poland Spain
  • A study to evaluate the effectiveness and safety of JNJ-88545223 in people with active psoriatic arthritis

    Recruiting

    Czechia Germany Hungary Poland Spain