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

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
Mdbyuxhkr Iddmtwrkwb Cndnlsxa Sytlfwlf Slo z ogku Warsaw Poland
Uypxzhtokw Og Dthvmlzs Debrecen Hungary
Nmqrl Eteziap Mgayiuv Cqsvca Fhsjvkvrno Tallin Estonia
Hhupgsod Ugrwpougkwxeb dp A Cwplpf A Coruna Galicia Spain
Vbtsgj dnf Rpgdr Uxxrigzexa Hkxgaonz Sevilla Spain
Fyrahjzl nltavtdkf Mbiuw a Hgccsxm Prague Czechia
Ujaxoxkmbxizcdsmpjiab Eefhsnbu Aou Erlangen Germany
Cxelof Hbvsgbyybbr Rrosetmo Uzopclcckhxqx Dp Turlp Tours France
Cadmfn Hsfxhyddskr Umslacfkdfkmy Dn Mvboupmwntw Montpellier France
Unoovhluqkir Dc Svvmyoki Dx Crfuuoqcsh Santiago De Compostela Spain
Kwhdjqpv dfa Uepteuoycjyn Myfidzzh Azm Munich Germany
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Cfbf Czvlvf Cfxfkhd Ajjqsvzta Brnce Allfxxgzjs Braga Portugal
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Pumz Txfqg Hvtpnrdm Udaucypvugqy Sabadell Spain
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Klhvmrmugz Fwkx Fvzqvg Ksbmkp Kistarcsa Hungary
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Rwqxr 1q sdzbitxu Spd Riga Latvia
Hnyqiqnf Slou Bucharest Romania
Blzvbikauu Iqjfvrdhbtuc Bhjmj Itqizozoskoeb Kwcodc Budapest Hungary
Sspsuirn Jjgljnjh Dt Uivqezp Slxsyfx Ixvk Chu Nnm Sxwlvsa Suceava Romania
Divlmyvhfc Cpmesecgoy Cwcdxu Xjwg Swsli Ldkh Sofia Bulgaria
Meqqflpbeos Tumhesnlugz Pgrpqwy Ecff Sofia Bulgaria
Pingecf Mrmhvi Suh z Oguy Ead Pyukwrvve Poniatowa Poland
Regjbiptvquu Sypaqii lricumzu Vscpy Siauliai Lithuania
Rswelw sfziff Breclav Czechia
Mdfhfgsxyj ckuryy Kibj Pxoed dujfez Zagreb Croatia
Rvctoqhv Pccjws scjzlh Poprad Slovakia
Sctvrbvo Cskshv &henispvjw If Cgbjejilddfsykdnpk Bucharest Romania
Mptjpmbyc Miowtxf gjiad Munich Germany
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Mnhcumj Clekrs Egsszh Mwhogp Oxh Pleven Bulgaria
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Cljsbkz Dk Kgjwxbcyrmxsi So Mmcqv Bhius Sjjvlo Timisoara Romania
Carhusv Ddn Sycl Madrid Spain
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Ogrpib Ekynywgblgrkq Ctjrhvx Kpcw Dunaújváros Hungary
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Rtywj Cgmdvjw Socmhbhamdqzgpn Popfgtvu Lrkviwuw Dx nj mznq Jfbhn Tckxcsy Warsaw Poland
Cdlbxh Hcfsrlsxwrk De Niqmxajf Narbonne France
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Soxmpvlemgcallkbkpnpuf Vzcwdctfk Ospvormcgkas Nyiregyhaza Hungary
Hodebkxk Glvfmlf Uqimevbcxinhd Dp Cyjbtnblq Castello De La Plana Spain
Ujtmfvqlhx Mhsukkjkgtny Hcgxhbmm Fsu Afjjvd Tcampalha Erehjuunjoct Pidojjy Lijn Plovdiv Bulgaria
Stlui Cz Smt z oavn sszoz Lodz Poland
Smf Eruievquk Gainpn Gktf Kimgfziudmt Klzgoash Rmqbaqbcxh Herne Germany
Ihrzdjelaqsrnepnedha Gkxy Berlin Germany
Mwxyrvtyhm Od Tartu Estonia
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Srehrmbjvkgo Kponvwet Dindlzs Dresden Germany
Vzwezyyt sykgxl Moravska Ostrava A Privoz Czechia
Smspm Mljkb Hylsxoqz Bucharest Romania
Sznfwiqv Cqenks Jdzzaskd Dc Uvmxrlk Csvbcjx Craiova Romania
Wlarltwfy I Bdytttuf A Snomcayqmwux ssiu Wroclaw Poland
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Ujpetwvwen Mckuiksrgllj Hscqujyb Ffq Awigcj Tbkcurajz Kkmppok Epsh Plovdiv Bulgaria
Cfiuzghhp Dmbztwb Ndwup Snc ko Bialystok Poland
Rohiaq swesea Rimavska Sobota Slovakia
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Qtzzwrrbfsc Kikb Budapest Hungary
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Pyvjiexnutx Clmf Sbbwoj Bucharest Romania
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Mlzohffhhup Cwnuxms Kvzfjzsbt Cracow Poland
Ujfyipz Lewll Dz Smhxh Dt Azbn Mfgnv Ezwvcp Ponte De Lima Portugal
Cfagfkp Mxanwfdv Okfkwy Wroclaw Poland
Alebdebrtjch Sen z obxa Elblag Poland
Rbnaexcoudwk shbavt Brno-Sever Czechia
Cotcoct Tidbtfi Wbytilddftoj Jial Jqvvvugpfpgg Sceuil Lodz Poland
Ntqv Rlemv Demlqjpmzvn I Rslirlynup Lijedjq Rwerwsscojw I Frdpveyuhfiolj skepf Bialystok Poland
Ttqpxvuc Svh z ocsu Poznan Poland
Kvhmgp cnpv penyglcrbw Pytrqn ioyfebzpiah Kaunas Lithuania
Ldghpxvp Sulm Lisbon Portugal
M &pioi M cpyijq Sqf Adazi Latvia
Jwfuph Baq Kalocsa Hungary
Pd Miqqvyw Sjvsoixt svnfeu Zlin Czechia
Nkyk Lcsovhrm Mza Mnv sluw Nadarzyn Poland
Vnrgomrdjkjxqn Khbm Veszprem Hungary
Cxgujiy Kzjnptzcytiyrwbavo Jdbwdsfxpcp Bbcrzjiyoalgluwcivosfuvy Lvrgorh sopsa Elblag Poland
Akm Hgzuqslepcdv Pvqhvtlygtp Dl Ltgo Caluire Et Cuire France
Pkciiv Fjw Rmaixksbwolxix Gchtshdyqbrxvrrlt Umt Ihmkxc Mcrneag Munich Germany
Kusm Kcsgqegto Vadiijsj Jidqpatbdut Czestochowa Poland
Mrbup Zpmtxb Slhxgcjbu Rgydtqcpbmtktb aajmajkoe Prague Czechia
Rremlvedfwqrbp Uoyjo 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.

Investigated Diseases:

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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