Study on Long-Term Safety and Efficacy of Litifilimab for Adults with Active Subacute or Chronic Cutaneous Lupus Erythematosus Resistant to Antimalarial Therapy

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What is this study about?

This clinical trial is focused on studying two types of skin conditions related to lupus: Subacute Cutaneous Lupus Erythematosus and Chronic Cutaneous Lupus Erythematosus. These conditions can cause skin rashes and lesions, and sometimes they may be associated with other symptoms throughout the body. The study is testing a treatment called BIIB059, also known as litifilimab, which is given as an injection under the skin. The purpose of the study is to evaluate the long-term safety and effectiveness of this treatment in adults who have these active skin conditions and have not responded well to or cannot tolerate antimalarial medications.

Participants in the study will receive the BIIB059 treatment over a period of time, and their health will be monitored to see how they respond to the medication. The study will look at how well the treatment works in reducing the severity of the skin conditions and any potential side effects that may occur. Some participants may receive a placebo, which is a substance with no active medication, to compare the effects of the treatment.

The study will last for up to 128 weeks, during which participants will have regular check-ups to assess their condition and any changes in their symptoms. The goal is to gather information on how safe and effective BIIB059 is for treating these types of lupus-related skin conditions over a long period. This information will help determine if the treatment can be a viable option for people with these conditions in the future.

1 joining the study

Upon joining the study, participants will be informed about the purpose and potential risks of the trial. Participants must provide informed consent, which means agreeing to participate after understanding the study details.

Participants must have completed the previous study, known as the parent study, and attended the last assessment visit at Week 52.

2 receiving the medication

Participants will receive the medication called BIIB059, also known as litifilimab. This medication is administered as an injection under the skin, a method known as subcutaneous injection.

The frequency and dosage of the medication will be determined by the study protocol and will continue for up to 128 weeks.

3 monitoring and assessments

Throughout the study, participants will undergo regular monitoring to evaluate the safety and effectiveness of the medication. This includes checking for any side effects or adverse reactions.

Participants will have their condition assessed using various measures, such as the Cutaneous Lupus Erythematosus Disease Area and Severity Index (CLASI) to track improvements in their condition.

4 completion of the study

The study is expected to last up to 128 weeks. During this time, participants will continue to receive the medication and attend scheduled assessments.

At the end of the study, participants will have a final assessment to evaluate the overall impact of the treatment on their condition.

Who Can Join the Study?

  • Participants must have completed the parent study (230LE301, Part A or Part B) on study treatment. This means they received treatment through Week 48 and attended the last study assessment visit at Week 52.
  • Participants must be able to understand the purpose and risks of the study.
  • Participants must be able to provide informed consent. This means they agree to participate after understanding the study details.
  • Participants must authorize the use of their confidential health information according to national and local privacy regulations.
  • The study is open to both male and female participants.
  • The study includes participants from vulnerable populations. This means people who might need special protection or care.

Who Cannot Join the Study?

  • Patients with active infections that are not well controlled. This means if you have an infection that is not being managed effectively, you cannot participate.
  • Patients who have had a serious allergic reaction to similar medications in the past. A serious allergic reaction can include symptoms like difficulty breathing, swelling, or severe rash.
  • Patients with other autoimmune diseases that are not stable. Autoimmune diseases are conditions where the immune system attacks the body’s own tissues.
  • Patients who are currently using other treatments that might interfere with the study medication.
  • Patients who are pregnant or breastfeeding. This is to ensure the safety of both the mother and the baby.
  • Patients with a history of substance abuse. Substance abuse refers to the harmful or hazardous use of substances like alcohol or drugs.
  • Patients with severe mental health conditions that are not well controlled. This includes conditions like severe depression or anxiety.
  • Patients who have participated in another clinical trial recently. This is to avoid any interference between different study medications.

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Other Sites

Site Name City Country Status
Fondazione IRCCS Ca Granda Ospedale Maggiore Policlinico Milan Italy
Ospedale San Raffaele S.r.l. Milan Italy
Karolinska University Hospital Solna Sweden
Azienda USL Toscana Centro Florence Italy
Hospices Civils De Lyon Lyon France
Centre hospitalier universitaire de Liege Liege Belgium
Universitair Ziekenhuis Gent Gent Belgium
Uniwersyteckie Centrum Kliniczne Warszawskiego Uniwersytetu Medycznego Warsaw Poland
University Of Pecs Pecs Hungary
Klinikum Oldenburg AöR Oldenburg In Holstein Germany
Hopital Tenon Paris France
Uniwersytecki Szpital Kliniczny Im.Fryderyka Chopina W Rzeszowie Rzeszow Poland
Universitaetsklinikum Erlangen AöR Erlangen Germany
Centre Hospitalier Universitaire De Toulouse Toulouse France
Centre Hospitalier Universitaire De Montpellier Montpellier France
Hopital Prive D Antony Antony France
University Multiprofile Hospital For Active Treatment St. Ivan Rilski EAD Sofia Bulgaria
Universitaetsklinikum Aachen AöR Aachen Germany
Elbe Kliniken Stade-Buxtehude gGmbH Buxtehude Germany
Hospital Universitario Puerta De Hierro De Majadahonda Majadahonda Spain
Hospital Del Mar Barcelona Spain
Hospital Universitario Rio Hortega Valladolid Spain
Hospital Cuf Descobertas S.A. Lisbon Portugal
Dkc 1 Ruse EOOD Ruse Bulgaria
Artromac N.O. Kosice Slovakia
Narodny Ustav Reumatickych Chorob Piestany Slovakia
Virgen del Rocío University Hospital Sevilla Spain
Rheinische Friedrich-Wilhelms-Universitaet Bonn Bonn Germany
Universita Degli Studi Di Brescia Brescia Italy
Dkc Fokus-5 Lzip OOD Sofia Bulgaria
IRCCS Ospedale Policlinico San Martino Genoa Italy
Centre Hospitalier Universitaire De Nice Nice France
Centro Hospitalar Universitario De Santo Antonio E.P.E. Porto Portugal
Charite Research Organisation GmbH Berlin Germany
Centre Hospitalier Universitaire De Caen Normandie Caen France
Diagnostic-Consultative Center Alexandrovska EOOD Sofia Bulgaria
Dermoklinika-Medyczne Centrum s.c. M.Kierstan J.Narbutt A.Lesiak Lodz Poland
Royalderm Warsaw Poland
Cfhptwbpa Uzntzpdtzxdbky Sgabgdktn Woluwe-Saint-Lambert Belgium
Hkpjzmvi Do Lw Sgldu Cdqn I Sojn Plq Barcelona Spain
Tmzblvzctei unl Swupefzeics Bpzxvthu Gddg Bad Bentheim Germany
Bpzypdrr Ujlyevvpwg Hygqtjlt Ctylss Besançon France
Unlhgwffatpokbrnngldv Mrgszvjc Aee Munster Germany
Mgcotmstebpnbjchalnghwllgl Hpgxeyvjvjgifhfl Halle (Saale) Germany
Usbiapbyaw Mvzopywtlxih Hcwmmhke fvh Aqtogb Tmvjsgqif Symfl Mxuymv &zidqoz Phfpas Pleven Bulgaria
Ajyicunuun Pincajct Hfafcoci Dc Pzigb Paris France
Auqvgif Utdje Svtjmwrcu Ljgjko Dz Bgqsnxl Bologna Italy
Hwosucsh Uubbhdjarrahe Hhhkwnem Tlqri y Pbszna Iaeexuey Cudmkj dxlvwkhzkjnfofudg (emcj Badalona Spain
Hdwcjfdw Vuce dthpviqq Barcelona Spain
Mwinfmj Cqyjjf Mgyvpfnmls Pcyzue Ogi Pleven Bulgaria
Hhkzstjl Uzhbchubjrnry dg A Cppnba A Coruna Galicia Spain
Mzzkazga mcrolbx arrxjug &rgszcq Mrwe &voxjid Sbbwe Sofia Bulgaria
Cmxanj Hzcqdapngi E Upjtaafptrgny Dg Cffwvpd Ehmjtp Coimbra Portugal

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

Trial status

Country Status Recruitment Start
Belgium Belgium
Not yet recruiting
16.02.2024
Bulgaria Bulgaria
Recruiting
16.02.2024
France France
Recruiting
16.02.2024
Germany Germany
Recruiting
16.02.2024
Hungary Hungary
Recruiting
16.02.2024
Italy Italy
Recruiting
16.02.2024
Poland Poland
Recruiting
16.02.2024
Portugal Portugal
Recruiting
16.02.2024
Slovakia Slovakia
Recruiting
16.02.2024
Spain Spain
Recruiting
16.02.2024
Sweden Sweden
Recruiting
16.02.2024

Trial locations

Investigated drugs:

BIIB059 (Litifilimab) is a medication being studied for its potential to help people with certain types of lupus, specifically subacute cutaneous lupus erythematosus and chronic cutaneous lupus erythematosus. These are conditions where the immune system mistakenly attacks the skin, causing rashes and other symptoms. This medication is being tested to see if it can safely and effectively reduce these symptoms over a long period. It is particularly aimed at people who have not had success with or cannot tolerate traditional treatments like antimalarial drugs. The goal is to find out if this medication can be a reliable option for managing lupus symptoms without causing significant side effects.

Subacute Cutaneous Lupus Erythematosus – This is a form of lupus that primarily affects the skin, causing lesions that are often red, scaly, and can appear in sun-exposed areas. The lesions may be ring-shaped or have a papulosquamous appearance, resembling psoriasis. Over time, these lesions can lead to skin discoloration but typically do not cause scarring. The condition can be triggered or worsened by sun exposure. It is often associated with mild systemic symptoms, such as joint pain or fatigue. The disease can fluctuate, with periods of flare-ups and remission.

Chronic Cutaneous Lupus Erythematosus – This form of lupus is characterized by persistent skin lesions that can lead to scarring. The most common type is discoid lupus erythematosus, which presents as round, red, and scaly patches that can thicken and scar over time. These lesions are typically found on the face, scalp, and ears, and can cause hair loss if they occur on the scalp. The condition is chronic, meaning it can last for a long time and may have periods of activity and inactivity. Sun exposure can exacerbate the lesions. Unlike systemic lupus, this form primarily affects the skin and is less likely to involve internal organs.

Trial ID:
2023-504863-17-00
Protocol code:
230LE305
Trial Phase:
Therapeutic confirmatory (Phase III)

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