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
University Of Debrecen Debrecen Hungary
North Estonia Medical Centre Foundation Tallin Estonia
Virgen del Rocío University Hospital Sevilla Spain
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
Centre Hospitalier Universitaire De Nice Nice France
CCAB Centro Clinico Academico Braga Associacao Braga Portugal
University General Hospital Of Heraklion Heraklion Greece
Athens Naval Hospital Athens Greece
University General Hospital Attikon General Hospital Of West Attica H Agia Varvara Chaidari Greece
University Multiprofile Hospital For Active Treatment Saint Georgi EAD Plovdiv Bulgaria
Revita Kft. Budapest Hungary
Twoja Przychodnia Poznańskie Centrum Medyczne Sp. z o.o. Poznan Poland
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
Dkc Fokus-5 Lzip OOD Sofia Bulgaria
Mbal Lyulin EAD Sofia Bulgaria
Med Polonia Sp. z o.o. Poznan Poland
Affidea Praha s.r.o. Prague Czechia
Kistarcsai Flor Ferenc Korhaz Kistarcsa Hungary
Praglandia s.r.o. Prague Czechia
Rigas 1. slimnica SIA Riga Latvia
Spitalul Judetean De Urgenta Sfantul Ioan Cel Nou Suceava Suceava Romania
Diagnostic Consulting Center XVII Sofia Ltd. Sofia Bulgaria
Meditsinski Tsentar-N.I Pirogov EOOD Sofia Bulgaria
Respublikine Siauliu ligonine VšĮ Siauliai Lithuania
Medicinski centar Kuna Peric d.o.o. Zagreb Croatia
Obudai Egeszseguegyi Centrum Kft. Dunaújváros Hungary
Fakultni Thomayerova nemocnice Prague Czechia
REUMA CENTRUM Specjalistyczna Praktyka Lekarska Dr n. med. Jakub Trefler Warsaw Poland
Centre Hospitalier De Narbonne Narbonne France
NIEPUBLICZNY ZAKŁAD OPIEKI ZDROWOTNEJ BIF-MED S.C. A. Wawiernia,M. Roykiewicz,R. Roykiewicz Bytom Poland
Medyczne Centrum Hetmanska Poznan Poland
Szabolcs-Szatmar-Bereg Varmegyei Oktatokorhaz Nyiregyhaza Hungary
Hospital General Universitario De Castellon Castello De La Plana Spain
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
Saint Maria Hospital Bucharest Romania
Spitalul Clinic Judetean De Urgenta Craiova Craiova Romania
Wromedica I Bielicka A Strzalkowska s.c. Wroclaw Poland
Lukmed 2 Sp. z o.o. Siedlce Poland
Dc-Med Michal Kowalski sp.k. Swidnica Poland
Bekes Varmegyei Koezponti Korhaz Gyula Hungary
Rcmed Oddzial Sochaczew Sochaczew Poland
Centre Hospitalier Jean Rougier Cahors France
Hospital Universitario Basurto Bilbao Spain
Etyka Osrodek Badan Klinicznych Tomasz Pesta S.K.A. Olsztyn Poland
Medman s.r.o. Martin Slovakia
Reumed Sp. z o.o. Lublin Poland
Twoja Przychodnia Nowosolskie Centrum Medyczne Sp. z o.o. Nowa Sol Poland
Ai Centrum Medyczne Sp. z o.o. Poznan Poland
Artromac N.O. Kosice Slovakia
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
Reumex s.r.o. Rimavska Sobota Slovakia
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
Policlinica CCBR S.R.L. Bucharest Romania
Instituto Portugues De Reumatologia Lisbon Portugal
MVZ Rheumatologie und Autoimmunmedizin Hamburg GmbH Hamburg Germany
Rheumatologische Schwerpunktpraxis Berlin Germany
Malopolskie Centrum Kliniczne Cracow Poland
Unidade Local De Saude Do Alto Minho E.P.E. Ponte De Lima Portugal
Centrum Medyczne Oporow Wroclaw Poland
Ambulatorium Sp. z o.o. Elblag Poland
Nova Reuma Domyslawska I Rusilowicz Lekarza Reumatologa I Fizjoterapeuty sp.p. Bialystok Poland
Termedia Sp. z o.o. Poznan Poland
Rheuma Medicus Sp. z o.o. Warsaw Poland
Medical Center Zara-Med EOOD Stara Zagora Bulgaria
Kaunas city polyclinic Public institution Kaunas Lithuania
Complex Rendelo Med Zrt. Szekesfehervar Hungary
Accellacare Espana S.L. Alcobendas Spain
PV Medical Services s.r.o. Zlin Czechia
NZOZ Lecznica Mak Med s.c. Nadarzyn Poland
Vital-Medicina Kft. Veszprem Hungary
Centrum Kliniczno-Badawcze J.Brzezicki B.Gornikiewicz-Brzezicka Lekarze sp.p. Elblag Poland
Ass Hospitaliere Protestante De Lyon Caluire Et Cuire France
Praxis Für Rheumatologie, Gastroenterologie Und Innere Medizin Munich Germany
K2J2 Katarzyna Viktoria Jachimowska Czestochowa Poland
MUDr. Zuzana Stejfova, Revmatologicka ambulance Prague Czechia
Revmatologicky Ustav Prague Czechia
Chirurgie Studenka s.r.o. Studénka Czechia
Mpjjwkoes Iiyufcsmwc Ckeuysyw Sfvqjvcs Sce z ojog Warsaw Poland
Hgnfviod Urtjgoofvvfdi dp A Cxvmah A Coruna Galicia Spain
Fuvuufok nxrxzykaj Mejjs a Hnbodmh Prague Czechia
Cjdvud Hwkshaflori Rfbpknga Ubzrmancridil Dc Tvyrd Tours France
Kykmbjvi ddm Umizplbwivyg Miojular Aqu Munich Germany
Fqjemybuw Pbtj Ld Ifeafwmzitwjm Bguxuruui Dqv Hedlkzdt Ullkwulxjjqxg Ld Pif Madrid Spain
Pwta Tyxgm Hedabgnu Uefvicdvensr Sabadell Spain
Hvdrfphr Sglq Bucharest Romania
Bukekhuxyg Irqanxhrvkbc Bztrg Imaflvngbower Kndyia Budapest Hungary
Pmpxctp Mbvrbw Sbt z Ooru Exc Ptcgjdidd Poniatowa Poland
Rpxrba ssejon Breclav Czechia
Rjgliwyx Pnsfgh svuuyr Poprad Slovakia
Spfhvkne Chklek &qwlpjjjkq Iw Cjgusvgtpmpxtypiyr Bucharest Romania
Mvgneswxw Mohugmg gbvrb Munich Germany
Qquooch Mphbrhl Csjztb Svzztn Bucharest Romania
Iemqqhuq dt Cxtmiggkoezx Hkjcrnjounv Ujgqrjspbdcsm dh Sbdmi Eacuubz (udwdiyj Saint Priest En Jarez France
Mnjtaas Cudwqz Elmgul Mzhfxk Oib Pleven Bulgaria
Cxzpag pmssfspqmsy Vilnius Lithuania
Coyebnl Mdjifs Cfemqqaeo di Sfzal Tlbzig Sq – Hbkdgxfw Lidqsolz Bangh Braga Portugal
Cumsqcy Db Knmlekceczuae Sk Mlntf Bhtqt Svdqpi Timisoara Romania
Cgyiohu Dvd Syxe Madrid Spain
Ugllr Ce Sqx z ojrl Dabrowka Poland
Cnwsnho Mcygzfhs Jnhxzdx Sil z obyc Warsaw Poland
Kznifjne bkfmzejg czwnfp Rvppmm (yfjymgqd Hysiwboc Coyasx Rmmvafy Rijeka Croatia
Pfvythbq Pjjqvrvi Lunhhfpa Pefg Di Hwp Mkv Pfkyi Hkchgu Poznan Poland
Ezd Zxgtbt Zamosc Poland
Kbpe Sqc z owyu Wołomin Poland
Erf Ltiqsw Lublin Poland
Ixzikvfzmtazzgxobjqv Gdwm Berlin Germany
Vgwnrzbh saoovl Moravska Ostrava A Privoz Czechia
Tvsbwalxgsy ueu Stbbayrowlc Baulmcbw Gtfx Bad Bentheim Germany
Rzzcpfzpexrj sidqgr Brno-Sever Czechia
Lpebtxib Sfad Lisbon Portugal
M &qjwj M cwgyds Slu Adazi Latvia
Jgvfgh Bxv 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

  • Long-Term Safety and Efficacy of Zasocitinib in Adults with Active Psoriatic Arthritis

    Recruiting

    3 1
    Investigated Drugs:
    Belgium Bulgaria Croatia Czechia Estonia France +7
  • Tulisokibart for Psoriatic Arthritis in Adults

    Recruiting

    2 1
    Investigated Diseases:
    Investigated Drugs:
    Germany Poland Spain