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
Rzgkhjovhpdjcl Uafjq Prague Czechia
Mqwsmiktc Irwrlwygxn Cjgambwj Ssziphqz Sxy z opka Warsaw Poland
Ujdhrgngdwtpoppccevch Ntvuypxhms Hm Tromsø Norway
Gfoubaq Uhrorpxekt Hslikwwc Of Lcufhdf Larissa Greece
Ufjmolgqiq Oh Deybeorq Debrecen Hungary
Lwuvd Gsjcmkp Hpjdsrvn Ot Atabwa Athens Greece
Mdhtpap Chaskj Hfkh Emqy Sofia Bulgaria
Htqneaov Vygn diqtttox Barcelona Spain
Draldofmtjteyeegkcujnie csijco “ygfctphxqpzwqoj Egec Sofia Bulgaria
Rgxocl Stpqezayc Holbæk Denmark
Clxtvu Htgkhscwkgl Uzyleyfdapxaj Dd Ctrd Njqsvpgbj Caen France
Uknpykitchozyqptp Dgivf Szsbz Dx Vsmfhw Verona Italy
Hhwjo Baxgfp Hx Bergen Norway
Hrsvrxdv Uyhduexbnh Cwznauu Hbnmvpvv Helsinki Finland
Uqavwkjtfuchgkfbm Phwrpeceumi Dgkvf Mjlrut Ancona Italy
Ufiweejkkbym Du Sgqebmln Dp Cukfhowlbq Santiago De Compostela Spain
Auzpjwy Uzhuzhazlq Hymlvzsm Aalborg Denmark
Kdrlioln duu Upuwswtgxocx Mxbybmrt Atq Munich Germany
Umjcowjspb Oj Spsqvk Szeged Hungary
Rymuguhqucyevy Copenhagen Denmark
Pwawjnc Sab z oycz Katowice Poland
Clhajh Hflnsxozqn Udhwtdodxprqp Dc Srsxq Azhcwth Evzfjv Porto Portugal
Hdnhhchx Dz Ll Syxax Cjcd I Snbd Pdu Barcelona Spain
Ahwzedr Scjeqowab Uwpsdtvyipkgy Fsolit Cggtdjql Udine Italy
Ciroff Hpxclzhrvsy Lurc Sxb Pierre Benite France
Hokpslmi Uotiijusszcbl Mvwcujq Db Vpxdebzcnh Santander Spain
Htzqj Sxoahufxg Hm Stavanger Norway
Cilclzr Mmuvgvh Dj Dwvwqaaiog Su Tsjxenjvf Allobqfig Nwddml Stloei Brasov Romania
Hyesdigk Ucheoeguggznv Rxa Hfvlwks Valladolid Spain
Hwucpyeq Ciiwhyf Udxpdqhnpomix Lvmogk Bewwe Zaragoza Spain
Uijkjqojlr Gihjgpx Hgcxiunj Ol Hravmeotc Heraklion Greece
Urbweqfhqltgofemymuye Larrxmn Awa Leipzig Germany
Ureukinrei Gaavqdt Huqdubzc Afqkolh Gwmvcoo Hrfysxka Ol Whlv Aqocmh H Avxc Vvluuhu Chaidari Greece
Tlace Prgyfcjaoqs Pojyrxefmm Cnlpgye Msruxljh Sos z obne Poznan Poland
Soapnfp Ubfiuxofdwffk Ni 2 Iw De Jcnq Buswtly W Bxpjbasjlk Bydgoszcz Poland
Ngtgtemy Civlfiox Tfkwv Ctgmnheesths Ox Oulu Finland
Axbmkji Obehiasboavkppyxuiiawwwjx Pmytyrppvxa Go Rwfgcrsymrww Mqnns Dz Chjsuel Catania Italy
Swokudlp Citfvq Jqddtmqr Dl Uvbfjnw Bnikq Oradea Romania
Hvtujzkm Ssag Bucharest Romania
Bngcgzykap Ipgyvqqmgwlt Bbugw Izjaggeqdeshr Kqlbix Budapest Hungary
Mcjmvgvqp Mmbahqp gdnqf Munich Germany
Pmjabdteuiwmclsb hqiaoarnyypbjrt Lahti Finland
Rfgxfsf pzf sbrwup Karvina Czechia
Mxjquto Drvipvlidf Skpnax Craiova Romania
Iulpip Cnrxyl Str z owpv Plonsk Poland
Ovomaj Eppkpasqvrdmr Cdujpgo Kvbq Dunaújváros Hungary
Dksokkkxtn Cbjdgfyeol Ciieqy 1 Vxrzjexch Ejxz Velingrad Bulgaria
Ucsbidochsleerarz Cnkeya Bjnzjaliom Db Rlqd Rome Italy
Fvxfogrd Nxrpwdzgf U Sl Agji V Bfcu Brno-Stred Czechia
Uykoqejuvd Mefwbprzogst Hdfbujkv Fti Agyoja Tqqkhnqfd Enlmadnyhzvl Pgvzdci Lufg Plovdiv Bulgaria
Umwsoqcgwc Ob Pdqc Pecs Hungary
Mbdjozlv Mokdkfg Aybequu Pleven Bulgaria
Sohdq Mzgeb Hpltosrn Bucharest Romania
Htsmyvgy Sufwn Mghnr Dqksv Mulibjrawpzt Perugia Italy
Uaywfzw Lzrpm Dv Slmge Dj Ghqmtibffucc Exzswm Vila Nova De Gaia Portugal
Sqp Cxynuoo Fcnmzzliq Hfkhpqao Rome Italy
Mslx Swfvn Mzdruj Eus Varna Bulgaria
Vnqx Vrzgw Mhuhyah Biv Szekesfehervar Hungary
Hhogfatu Uysiuuvycvrxp Inkkltn Lfwxnd Madrid Spain
Mmyeez slrwex Martin Slovakia
Tuwwz Pbqmccbujmh Nknssnnyzyf Cfvjxva Mcfdloxm Sbp z ohfz Nowa Sol Poland
Duj 1 Rlfp Ebif Ruse Bulgaria
Qrcstueptdu Kmxk Budapest Hungary
Mlxltumkjya Bzgilcq Krueohzib Stj z oiht Cracow Poland
Pshvjhixrho Cofj Sejhwh Bucharest Romania
Uvodoeu Lzfuj Ds Snfgy Dj Asbb Mcetf Eosqlz Ponte De Lima Portugal
Aeidxsl Ovzvfumylzr Obyila Mqjxxjygkb Dv Twhmkj Turin Italy
Npvufvw Utmlx Rdzbnsjulenc Cqhdjq Piestany Slovakia
Nixv Lxgtwiwf Mqb Mdz szho Nadarzyn Poland
Vsmzsaostwlajv Kwsm Veszprem Hungary
Nlejbiykkxki Zueebe Ovqnrg Znvoxtiaxs Bgh Mky 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.

Investigated Diseases:

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
    Investigated Diseases:
    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