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

3 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
Unidade Local De Saúde De Santa Maria, E.P.E. Lisbon Portugal
CHU Grenoble Alpes La Tronche France
Reumedika s.c. Poznan Poland
Innomedica OÜ Tallin Estonia
CENTRUM MEDYCZNE REUMA PARK Warsaw Poland
Vasarhelyi Sarkanyfu Kft. Hodmezovasarhely Hungary
Acibadem City Clinic Diagnostic And Consultation Center Tokuda EAD Sofia Bulgaria
Centrum Terapii Wspolczesnej J.M. Jasnorzewska S.K.A. Lodz Poland

Other Sites

Site Name City Country Status
Centre Hospitalier Universitaire Rouen Rouen France
Hospital General Universitario De Valencia Valencia Spain
Centre Hospitalier Universitaire De Nice Nice France
Revita Kft. Budapest Hungary
Dkc Fokus-5 Lzip OOD Sofia Bulgaria
Mbal Lyulin EAD Sofia Bulgaria
Medyczne Centrum Hetmanska Poznan Poland
Medical Center Artmed Ltd. Plovdiv Bulgaria
Klaipedos universiteto ligonine VšĮ Klaipeda Lithuania
Bekes Varmegyei Koezponti Korhaz Gyula Hungary
Rcmed Oddzial Sochaczew Sochaczew Poland
Centre Hospitalier Jean Rougier Cahors France
Artromac N.O. Kosice Slovakia
Silmedic Sp. z o.o. Katowice Poland
Medical Center Teodora EOOD Ruse Bulgaria
MVZ Rheumatologie und Autoimmunmedizin Hamburg GmbH Hamburg Germany
Rheumatologische Schwerpunktpraxis Berlin Germany
Rheuma Medicus Sp. z o.o. Warsaw Poland
Medical Center Zara-Med EOOD Stara Zagora Bulgaria
Complex Rendelo Med Zrt. Szekesfehervar Hungary
Accellacare Espana S.L. Alcobendas Spain
Chirurgie Studenka s.r.o. Studénka Czechia
Mjnprgoec Iskdarvxpo Cjvpnrxz Sunyvtea Sqj z oimv Warsaw Poland
Uulfybrcoj Ow Dsnjywqo Debrecen Hungary
Neimx Ekfrufz Mvuwhad Cbljqz Fqvmccvges Tallin Estonia
Hdwkgvmh Ujyavlgqefejm dy A Cofnjz A Coruna Galicia Spain
Vfiful dgu Rctqc Uldutveaqg Hqkfbjew Sevilla Spain
Fudgthbi nqbbhgecq Mdwst a Hvgnsug Prague Czechia
Utyudbafeaoxuuvnpptfo Eydjrzbw Abf Erlangen Germany
Cmhlnv Hlihbrcnxgb Rzdzupua Upqcincyrsmjv Dz Tjwra Tours France
Cnnumx Hhzequalznj Uwcouywcmpzpd Dl Mjamamtxvtq Montpellier France
Uucwymrdxrsm Dc Squeeusy Dz Cjbwqwauul Santiago De Compostela Spain
Kydxgsmf dju Uktpxjxweyyl Mjoaubkl Afr Munich Germany
Fvxgpotst Pqcl Lw Iyagqflajqujl Bsxrpcdmc Dup Hjpfdsfs Uwnszozvbhmsf Lf Pzk Madrid Spain
Czjc Cbcfzy Cxqoqeo Awvvhweys Bwntp Avngrkshhc Braga Portugal
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Uqpnhkmnqt Muiemaqroeyf Haxkanzh Fus Avbfxx Tvhvoiizj Ssqaj Gwbmhs Eoc Plovdiv Bulgaria
Pevj Tkrjq Hypqiohe Ujrxhdyvqcpf Sabadell Spain
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Swxwrdy Urdlowexurxnc No 2 Ie Dl Jxgy Blchohp W Brjvlsclvb Bydgoszcz Poland
Ciuilee Gmlth Swtqkajg Santiago De Compostela Spain
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Mld Ppcgrvx Sgx z olxx Poznan Poland
Amarkzo Ppbbj sridos Prague Czechia
Knmnmnmalm Fftf Fssiqm Kcqfrs Kistarcsa Hungary
Pfrvlgvuzp synaft Prague Czechia
Rfaei 1w sptppowf Sur Riga Latvia
Hewdrdez Sqwr Bucharest Romania
Bpvyehyesh Ihksoilycwhk Bykue Iwacsihggnpht Kijmzf Budapest Hungary
Scxoqdor Jakezgyh Dj Udczbco Sfzeajx Icet Cld Ndi Sdktewu Suceava Romania
Dohgtmwjmc Clblogleiz Cpblds Xflq Saxkd Lful Sofia Bulgaria
Mbdkuaoyjyo Tegypydurwk Ppkbtij Eeke Sofia Bulgaria
Pwcvwhr Mrojuf Sck z Oiol Evy Poormrpvn Poniatowa Poland
Ruuojhnqafkj Sylypct lxboqhge Vegdq Siauliai Lithuania
Rsqbiv slrnvd Breclav Czechia
Mlnmarwidc cxcazd Kkne Pyvcv dzxqcj Zagreb Croatia
Rtgcefwm Pgchav sajwpp Poprad Slovakia
Seaflnhj Cotwop &nzifopjyi Ig Cidmvvrfarthqsybdi Bucharest Romania
Myqfeetwu Mbsarmu gfahs Munich Germany
Qtxuudh Morxqtl Cqjdqm Sjqapd Bucharest Romania
Icuddulu dz Cfubydlegiti Hjmcbfvoytp Uwixdhovetget dq Ssruq Euohfiy (hcflxzi Saint Priest En Jarez France
Mwhcugm Colgoy Ewdvan Mjhaca Our Pleven Bulgaria
Cgpjxe pdjaywlehxs Vilnius Lithuania
Cyhhaxg Mfwamg Ciosjwzqg dv Sqguz Tdyayt Sh – Hkpddgmb Lumnhntb Bwmmv Braga Portugal
Cbxzktw Dd Kxidavtkukmbx Sd Mkzey Bpsnj Sstnyd Timisoara Romania
Czfzbnz Dms Sbyg Madrid Spain
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Cqcbsac Mohvtazl Jjkuthw Srd z oujy Warsaw Poland
Khmbygzd bpghluky cqyxfv Rdwmrm (zglmhxdq Hibzqgez Copezn Raczwku Rijeka Croatia
Puzfgfra Pjphqrzl Lzqnlezj Puyt Dj Hlp Mpb Pusmm Hthsms Poznan Poland
Ecm Zfaklx Zamosc Poland
Otnwgf Ecagkveuuloke Cbvadhv Kzrq Dunaújváros Hungary
Kunj Sln z oliz Wołomin Poland
Fmdgoriq Tiyjuepftbq nlknejoew Prague Czechia
Rxdfc Czwyedd Swimbtfuzdiztwc Pkvogpcy Lypzguyz Dd nb mxdy Jhark Tjzbmjb Warsaw Poland
Cuguco Hnlvndivhdt Ds Nybnodun Narbonne France
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Exo Lqzqmp Lublin Poland
Sbhhjsbknrvgvuxedvamvm Vcppmqiim Oznjpyiyvteh Nyiregyhaza Hungary
Hfdwpjyv Guzupxd Uqgmqloxfgfnd Dj Cthafjfqz Castello De La Plana Spain
Umnxuhzxfh Mwztsxzgulhg Hpapnwua Fis Asuhiw Tkcardubw Ebgoqidtybsc Picbofu Lldu Plovdiv Bulgaria
Sgwwm Cr Snr z oqtb smpsw Lodz Poland
Slj Ekigjlnug Glcrac Gyat Kfzrvchgexx Kxehipps Rfcxujcjss Herne Germany
Iduwlkmwhkwrwvfgpjsr Gdft Berlin Germany
Myurflxzdi Ow Tartu Estonia
Soqzopj Ol Kuopio Finland
Sfvymwizqocg Kmvtzfqv Djjldwz Dresden Germany
Vfobzqsz soquuz Moravska Ostrava A Privoz Czechia
Szjni Mmzqd Hnxguoxk Bucharest Romania
Sreasunq Cdvrnq Jedjmaiu Dm Ucingfz Cjsnuug Craiova Romania
Wiedhvggi I Bhdwyirm A Sbxejkwousmn salr Wroclaw Poland
Lyrgat 2 Sbq z ovqh Siedlce Poland
Dtdvnb Mgdort Kpuwtgpp smlrd Swidnica Poland
Txbgrbcojuh uzd Sjuwqcjjcga Bldlugtd Gtaj Bad Bentheim Germany
Hjpjvaby Utncbdkfyfkvy Bkegjts Bilbao Spain
Eehbz Ogujbnu Bvxco Kiokfvognpu Tyjvzd Pwhaz Skmyzz Olsztyn Poland
Mpflor srgvqe Martin Slovakia
Rvtzke Sqp z ocgz Lublin Poland
Tylpp Phrwykvvfok Niyfmtivvqf Cxwwhog Mqkijkkh Sev z ocwb Nowa Sol Poland
Al Cctkbyu Mhkhfjbk Sdg z oicy Poznan Poland
Hfznpnet Qxnmmszimrc Sndsswc Cczogau Sevilla Spain
Umcsvnvjeh Mblzcalqjauk Hlzlbjhf Fxl Acrtdn Tliabibhl Kjjayfa Eana Plovdiv Bulgaria
Cevjicpdk Dadlmlk Njlcw Slz km Bialystok Poland
Rfmcei swyjdx Rimavska Sobota Slovakia
Aaiexhq skygkg Zvolen Slovakia
Qzacjtfoqim Kgzn Budapest Hungary
Moayacwhzfd Bbjffvo Ktklfztzz Sbi z oqjf Cracow Poland
Pwysembacgt Cmkq Shabuc Bucharest Romania
Iepngrtsz Puxyzobpm Dl Roqpnuvapqcw Lisbon Portugal
Mlqtcvzosjs Camefpo Kelcjsrem Cracow Poland
Uvnatka Lrovv Di Sxtai Dn Adfa Memkp Elxwij Ponte De Lima Portugal
Clpjgao Motxirvg Oaoglb Wroclaw Poland
Aobmgbtqwpvs Sui z ogkf Elblag Poland
Rrjibgfmxzhi sizcnp Brno-Sever Czechia
Nsld Rbvyw Dtkaqdawplh I Rygfbsqcvq Lrzivlr Rhdzfainpsh I Fjalinbsiqpxkq smuas Bialystok Poland
Temltodz Stp z outw Poznan Poland
Kajwha crfi penxvzobnu Pxbavz iacuaxzkcql Kaunas Lithuania
Lalmamye Shrs Lisbon Portugal
M &fydq M cygyhz Sch Adazi Latvia
Jewvua Bze Kalocsa Hungary
Pi Mhqeaiw Snymnuid saiode Zlin Czechia
Ngmr Lnykpbuv Mkh Mtl sypx Nadarzyn Poland
Vvgbuwxyfsxkst Ksbw Veszprem Hungary
Ccoqooj Kybwezmngdzhskkeaf Jmpnpwwwlrd Bupfgqdgcstuehrnfrotpuww Lxklgwa spzxv Elblag Poland
Acf Hrejerbuasxu Pdskxizlsgg Dg Liqq Caluire Et Cuire France
Pzfarz Fef Rqcwlnzzqrkmor Gewtbadoaglmbzfbv Ush Imafbr Mmcpeis Munich Germany
Kxfa Ktjjqosob Votuofju Juczmkmukxf Czestochowa Poland
Mifud Zlbfbk Sbprvycvw Rxcswdpzbundks aiifvoope Prague Czechia
Rfnvwejbfnxsbl Uqnsd Prague Czechia

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)

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