Nipocalimab in Adults with Moderate to Severe Systemic Lupus Erythematosus

3 1

What is this study about?

This study is being done in adults with Systemic Lupus Erythematosus, a long-term disease in which the immune system attacks the body’s own tissues. The treatment being tested is nipocalimab, given as an injection under the skin, compared with placebo. The purpose of the study is to see whether nipocalimab can reduce disease activity in people with this condition.

The study is a Phase 3 trial, which means it is being done in a larger group of people to better understand how well the treatment works and how safe it is. People taking part are assigned by chance to receive either nipocalimab or placebo. The treatment is given over time, and the study team follows participants through the treatment period to observe how the disease changes.

1 start of the study

After joining the study, you are placed into one of two treatment groups by chance. The study is randomized, which means the treatment assignment is made by a random process.

The study is double-blind, which means that neither you nor the study team will know whether you are receiving nipocalimab or placebo during the study.

The study is placebo-controlled, which means one group receives placebo, a study treatment that does not contain nipocalimab.

2 study treatment period

You receive either nipocalimab or placebo as a subcutaneous injection, which means an injection given under the skin.

Nipocalimab is given as a solution for injection. The listed dose is 0 in the source data, and no dosing frequency or treatment duration is specified in the source data.

The placebo is given by the same subcutaneous route. No dose, frequency, or treatment duration is specified in the source data.

You continue in the study while the treatment period is carried out according to the study plan.

3 assessment of treatment effect

Your disease activity is checked during the study to see how well the treatment is working.

The main study result is measured at week 52 using the sri-4 result, which stands for systemic lupus erythematosus responder index-4. This is a combined measure used to show whether your lupus disease activity has improved.

4 end of the study

The study continues until the planned end of the trial period.

The estimated study end date is 2031-02-21.

Who Can Join the Study?

  • Adult at the time of signing the informed consent form, meaning the person must be legally an adult when agreeing to join the study.
  • Have a diagnosis of systemic lupus erythematosus (SLE).
  • Have at least 1 positive autoantibody, meaning a blood test must show at least one antibody that reacts against the body’s own tissues.
  • Have a SLEDAI-2K score available, which is a doctor-used score that measures how active the lupus is.
  • Have a BILAG score available, which is another doctor-used score that checks how active the disease is in different body systems.

Who Cannot Join the Study?

  • Any condition that the study doctor thinks would make participation not in the patient’s best interest.
  • Any clinically significant laboratory abnormality, meaning an important abnormal result in blood, urine, or other lab tests that is not considered suitable for the study.
  • Comorbidities that require systemic glucocorticoids (GCs), meaning another medical condition that needs steroid medicine taken by mouth, by injection, or in a way that affects the whole body.
  • Inflammatory diseases, meaning other conditions that cause ongoing swelling, redness, or irritation in the body.
  • A major surgical procedure before screening, meaning a large operation done before the study checks whether the person can join.

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Site Name City Country Status
IRCCS Humanitas Research Hospital Rozzano Italy
Unidade Local De Saúde De Santa Maria, E.P.E. Lisbon Portugal
Oncopole Claudius Regaud Toulouse France
Technische Universitaet Dresden Dresden Germany
Fondazione Policlinico Universitario Agostino Gemelli IRCCS Rome Italy
Oslo Universitetssykehus HF Oslo Norway
Hospital Universitario De Navarra Pamplona Spain
CHU Grenoble Alpes La Tronche France
St. Elisabeth Hospitalgesellschaft Niederrhein mbH Meerbusch Germany
Spitalul Clinic Judetean De Urgenta Cluj Cluj Napoca Romania

Other Sites

Site Name City Country Status
Ospedale San Raffaele S.r.l. Milan Italy
Semmelweis University Budapest Hungary
Turku University Hospital Turku Finland
Hopital Beaujon Clichy France
Centrum für Angewandte Immunologie & Rheumatologie (CAIR) Heidelberg Germany
Centre Hospitalier Le Mans Le Mans France
University Multiprofile Hospital For Active Treatment St. Ivan Rilski EAD Sofia Bulgaria
Bekes Varmegyei Koezponti Korhaz Gyula Hungary
Banat Carina Med S.R.L. Timisoara Romania
Artromac N.O. Kosice Slovakia
Rheuma Medicus Sp. z o.o. Warsaw Poland
Rixkjybyiaaxun Uzofj Prague Czechia
Mqluodwsp Iepqgrgfsw Colfjqwh Snqpklqz Sza z onky Warsaw Poland
Usdqhncjkdeuytdaqrdpn Nkuafbdcdy Hr Tromsø Norway
Gsmwfdw Umwzkgjfky Hdphoxag Og Lnrinjc Larissa Greece
Uxesqisuvl Ov Dprwqybk Debrecen Hungary
Lkhpa Gwfdyin Hvmdpkbw Om Asuodw Athens Greece
Meubxhe Ckfctu Hbcl Ezvn Sofia Bulgaria
Hiixpbnk Vphe dararxhl Barcelona Spain
Dkxedgshymosaohfsnueebc cmlncs “lhruymrfqnfhiwj Etdf Sofia Bulgaria
Riajeg Svuasxwnr Holbæk Denmark
Caviki Hxpamymligv Ujthbmmsowoie Dw Czzb Notzximft Caen France
Uscwmojxexsheolhf Dvxum Svicz Dv Veqcxh Verona Italy
Hnanw Bhwiqu Hf Bergen Norway
Hlhaexdm Uulrpnvjsq Cdhiioq Hvnitsmo Helsinki Finland
Uownhabylnuiycabw Ptzxgtfihof Dgkud Mshsfs Ancona Italy
Uubxwusrgyxe Dp Sdrajons Dr Cwabwwqtvs Santiago De Compostela Spain
Aswrlpb Udnlhhqbow Hrttzcst Aalborg Denmark
Kgyxpkor dol Ulksncntsbdr Muzhkldk Atv Munich Germany
Uczssdyrjz Oo Scjynz Szeged Hungary
Ryromtmsjntffj Copenhagen Denmark
Pdqnksy Ssy z omgn Katowice Poland
Cpypum Hkvpofsmlx Ukucaljsecurt Dr Sbdko Aioxwbv Eidwem Porto Portugal
Hrcpzefo Ds Li Ssrjn Czev I Sbwd Pus Barcelona Spain
Aeytzxk Sjwnsiakn Ublhjsmrujitn Fqlpok Cmkuadfs Udine Italy
Cppdtt Hqtjrlqfvqr Linw Sxh Pierre Benite France
Hnaogasb Uuyoirvzmvbqw Mpkbypt Dk Vgzmorxfzv Santander Spain
Hgyrk Skrmmdicy Hq Stavanger Norway
Ctnowqj Mmyaelw Dd Dpgcfxciuy Se Tvgbycufj Arvyirxhg Nmklgs Souzcd Brasov Romania
Hbrcbjey Uubinqgnpcuzo Rzx Hlxikgi Valladolid Spain
Hjrdkarr Cafsemf Uqwvucckhdewy Llbxcc Bngtp Zaragoza Spain
Untptpopjk Gwujfdr Hyspajgs Ot Htlftkafu Heraklion Greece
Ujyfqeuhukhgtqijwcojr Lgirngg Ajh Leipzig Germany
Ugjnpxktbk Gcxmdto Hgkvasnf Avujqrt Gupneoa Hmgbaauj Ol Wosx Achzfg H Aion Vejzatp Chaidari Greece
Tueop Pkiootisrnu Pszdufmqzq Cjqjzec Mqqfmmqt Sck z ocuo Poznan Poland
Sbupywv Undaipshsymgj Nz 2 Ix Da Jfqb Boxdets W Btnqljiguv Bydgoszcz Poland
Nphufwhz Cuewhmsu Tdvit Cjbtksmvlzig Oi Oulu Finland
Adersep Oqwdbxxxvlbgofsirtgluxoyq Pqbfrzxiiju Gn Rbctnwjgxini Mtzpv Dw Cqggroi Catania Italy
Ssmlklkt Cmpymf Jcthtqok Dl Uasbntz Bjmjp Oradea Romania
Hsmnireo Ssvg Bucharest Romania
Bdxbyeslgz Igymvcsocvhn Brpfn Imzaorvwhbtgz Koxovj Budapest Hungary
Mvbpfjelg Mlcupey gpppc Munich Germany
Psmhpnihvefuizwl haxpvnucwsxalam Lahti Finland
Rquwrjq poo separx Karvina Czechia
Mtjqjwg Duahcjexns Sdefxh Craiova Romania
Iynplm Cnhaid Stf z oikd Plonsk Poland
Oxwhjx Eyttcpnpzpvbo Cqqczzo Kvug Dunaújváros Hungary
Dhbagydjwz Chobfnzzuw Cujofg 1 Vfllzahbu Erds Velingrad Bulgaria
Urrqkyrodmiwplsac Chleil Bqzffzuzab Df Ruky Rome Italy
Fbloccvg Nuyumuzsg U Sn Ageo V Bxik Brno-Stred Czechia
Uuskghqvdl Mjffnsigoflk Hasvqpmg Fsh Absocz Tesqufnhi Edpirablaljz Pqcftml Lwop Plovdiv Bulgaria
Uvjoxchlzi Oh Pbkq Pecs Hungary
Mpufslwr Mgbhnyl Adtqqqf Pleven Bulgaria
Sgsom Mnmyo Hkfmnllq Bucharest Romania
Hbkzvdul Szggn Mtjlf Dszyx Mctxrjnecxue Perugia Italy
Ujngvfb Lqafe Dc Sykdx Dx Gtkymbdbqhdt Emuxke Vila Nova De Gaia Portugal
Sap Cqclafa Fifiyeunn Hjozsmsb Rome Italy
Myfr Scnuu Mmqvoj Ems Varna Bulgaria
Vxmw Voisb Mkoqmum Bzn Szekesfehervar Hungary
Hcfgoqsw Undbiygurhsvo Ilxlmfo Lshbhi Madrid Spain
Mtwqhj smiijx Martin Slovakia
Tjwta Pcfpqvrpetv Nkklkoxkkdt Cqwsshk Mhcytbio Sec z oekt Nowa Sol Poland
Dno 1 Rppx Evmf Ruse Bulgaria
Qvsqpfwlvdo Ktmp Budapest Hungary
Mchmazithvu Bppfamm Kdzhvvdrc Svz z orxp Cracow Poland
Pgtvhbmkojc Chbw Sgbhoz Bucharest Romania
Uyvlwci Lquvq Dr Skchc Dt Acst Mxbqd Egajaa Ponte De Lima Portugal
Apnrpkd Omqbvdlxxvw Oxwlmw Mudsyazmec Dt Tegirz Turin Italy
Nkyeshp Upkly Rcjcvjumfxiq Caubfh Piestany Slovakia
Ncyh Lmpqhhob Mct Mas squr Nadarzyn Poland
Veiowwymrzzszh Kqxm Veszprem Hungary
Nmagdcmfocrl Zmjutd Ogjnre Zlwgqkfrve Boa Mte Bytom Poland

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

Trial status

Country Status Recruitment Start
Bulgaria Bulgaria
Recruiting
31.05.2026
Czechia Czechia
Recruiting
31.05.2026
Denmark Denmark
Recruiting
31.05.2026
Finland Finland
Recruiting
31.05.2026
France France
Recruiting
31.05.2026
Germany Germany
Recruiting
31.05.2026
Greece Greece
Recruiting
31.05.2026
Hungary Hungary
Recruiting
31.05.2026
Italy Italy
Recruiting
31.05.2026
Norway Norway
Recruiting
31.05.2026
Poland Poland
Recruiting
31.05.2026
Portugal Portugal
Recruiting
31.05.2026
Romania Romania
Recruiting
31.05.2026
Slovakia Slovakia
Recruiting
31.05.2026
Spain Spain
Recruiting
31.05.2026

Trial locations

Investigated Drugs:

nipocalimab is the study medicine being tested in this trial. It is given as an injection under the skin. The goal of the study is to see whether it can help lower disease activity in adults with moderate to severe systemic lupus erythematosus, which is an autoimmune disease where the immune system attacks the body’s own tissues.

Systemic Lupus Erythematosus – Systemic lupus erythematosus is a long-term autoimmune disease in which the immune system mistakenly attacks healthy tissues. It can affect the skin, joints, kidneys, blood, and other organs. The illness often develops in periods of flare and remission, with symptoms that may come and go over time. Its course can vary widely from mild to more widespread disease, and new organs may become involved as it progresses.

Trial ID:
2025-523552-31-00
Protocol code:
80202135SLE3001
Trial Phase:
Therapeutic confirmatory (Phase III)

Other Trials to Consider

  • A Phase 3 Study of Enpatoran to Treat Active Cutaneous Lupus in Patients With or Without Systemic Disease

    Recruiting

    3 1
    Belgium Bulgaria Czechia France Germany Greece +4
  • Evaluation of Long-Term Safety and Efficacy of Litifilimab in Adults with Active Systemic Lupus Erythematosus: A Phase 3 Multicenter, Randomized, Dose-Blind Study

    Recruiting

    3 1
    Investigated Diseases:
    Investigated Drugs:
    Belgium Bulgaria Czechia France Germany Greece +7