Effectiveness And Safety Of MK-6194 In Adult Patients With Lupus (MK-6194-006)

RECRUITING

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The purpose of this study is to assess the efficacy and safety of MK-6194 in adult patients with Lupus. The primary hypothesis is that at least 1 of the MK-6194 arms is superior to placebo in the primary endpoint of percentage of patients with systemic lupus erythematosus responder index (SRI-4) response at Week 28.

Conditions:

🦠 Systemic Lupus Erythematosus

🗓️ Study Start (Actual) 27 December 2023

🗓️ Primary Completion (Estimated) 22 January 2026

✅ Study Completion (Estimated) 9 July 2027

👥 Enrollment (Estimated) 270

🔬 Study Type INTERVENTIONAL

📊 Phase PHASE2

Locations:

📍 La Palma, California, United States

📍 Denver, Colorado, United States

📍 Clearwater, Florida, United States

📍 Plantation, Florida, United States

📍 Charlotte, North Carolina, United States

📍 DeSoto, Texas, United States

📍 Sherbrooke, Quebec, Canada

📍 Temuco, Araucania, Chile

📍 La Serena, Coquimbo, Chile

📍 Santiago, Region M. De Santiago, Chile

📍 Beijing, Beijing, China

📍 Guangzhou, Guangdong, China

📍 Guiyang, Guizhou, China

📍 Nantong, Jiangsu, China

📍 Shanghai, Shanghai, China

📍 Medellín, Antioquia, Colombia

📍 Barranquilla, Atlantico, Colombia

📍 Chía, Cundinamarca, Colombia

📍 Zipaquira, Cundinamarca, Colombia

📍 Cali, Valle Del Cauca, Colombia

📍 Pessac, Aquitaine, France

📍 Toulouse, Haute-Garonne, France

📍 Montpellier, Herault, France

📍 Saint Priest En Jarez, Loire, France

📍 Lille, Nord, France

📍 Lyon, Rhone-Alpes, France

📍 Ciudad de Guatemala, Guatemala

📍 Guatemala, Guatemala

📍 Rome, Roma, Italy

📍 Siena, Toscana, Italy

📍 Nagoya, Aichi, Japan

📍 Kawasaki, Kanagawa, Japan

📍 Sendai-shi, Miyagi, Japan

📍 Tomigusuku, Okinawa, Japan

📍 Izumo, Shimane, Japan

📍 Shimotsuga, Tochigi, Japan

📍 Itabashiku, Tokyo, Japan

📍 Shinagawa, Tokyo, Japan

📍 Chiba, Japan

📍 Okayama, Japan

📍 Osaka, Japan

📍 Lembah Pantai, Kuala Lumpur, Malaysia

📍 Kuantan, Pahang, Malaysia

📍 Taiping, Perak, Malaysia

📍 Bydgoszcz, Kujawsko-pomorskie, Poland

📍 Lublin, Lubelskie, Poland

📍 Krakow, Malopolskie, Poland

📍 Bialystok, Podlaskie, Poland

📍 Bytom, Slaskie, Poland

📍 Poznan, Wielkopolskie, Poland

📍 A Coruña, La Coruna, Spain

📍 Valencia, Valenciana, Comunitat, Spain

📍 Barcelona, Spain

📍 Sevilla, Spain

📍 Valladolid, Spain

More locations available...

📋 Eligibility Criteria

Description

Inclusion Criteria:

* Has a diagnosis of systemic lupus erythematosus (SLE) ≥6 months prior to Screening.
* Is taking at least 1 background therapy (1 immunosuppressant or dapsone and/or 1 antimalarial and/or oral corticosteroids) for SLE.
* Has + antinuclear antibody (+ANA) (titer ≥1:80) or positive anti-double-strand deoxyribonucleic acid (dsDNA) antibody or positive anti-Sm antibody, or positive anti-SSA/Ro antibody.
* Has the presence of at least one of the following manifestations of SLE: Active lupus rash with CLASI-A erythema and scale/hypertrophy combined score \>2, or \>2 tender and swollen joints in wrists, metacarpophalangeals (MCPs), or proximal interphalangeals (PIPs).
* Has a hybrid Systemic Lupus Erythematosus Disease Activity Index (SLEDAI) total score of ≥6 and clinical hybrid SLEDAI score of ≥4.

Exclusion Criteria:

* Has a concurrent clinically significant disease or clinically relevant laboratory abnormalities, or a history of any illness or medical condition that, in the opinion of the investigator, might confound the results of the study or poses an additional risk to the participant by their participation in the study.
* Has symptomatic heart failure (New York Heart Association class III or IV) or myocardial infarction or unstable angina pectoris within 6 months prior to Screening.
* Has a severe chronic pulmonary disease requiring oxygen therapy.
* Has a transplanted organ which requires continued immunosuppression.
* Has a known systemic hypersensitivity to IL-2, or modified IL-2 including MK-6194, or its inactive ingredients.
* Has a known history of lymphoproliferative disease, including lymphoma, or signs and symptoms suggestive of possible lymphoproliferative disease, such as lymphadenopathy and/or splenomegaly.
* Has drug-induced cutaneous lupus erythematosus (CLE) and/or drug-induced SLE in the setting of continued treatment with a causative agent.
* Has active or unstable neuropsychiatric lupus including but not limited to the following: seizure, new or worsening impaired level of consciousness, psychosis, delirium or confused state, aseptic meningitis, cranial neuropathy, cerebrovascular accident, ascending or transverse myelitis, chorea, cerebellar ataxia, mononeuritis multiplex, or demyelinating syndromes.
* Has a diagnosis of Antiphospholipid Syndrome with history of vascular thrombosis, catastrophic APS, or pregnancy morbidity within 6 months prior to Screening.
* Has a history of any malignancy, except for successfully treated non-melanoma skin cancer or localized carcinoma in situ of the cervix.
* Has an active or clinically significant infection requiring hospitalization or treatment with anti-infectives.
* Has evidence of active tuberculosis (TB), latent TB, or inadequately treated TB.
* Has confirmed or suspected COVID-19 infection.
* Has had major surgery within 3 months prior to Screening or has a major surgery planned during the study.
* Is taking more than 1 immunosuppressant.
* Is taking more than 1 oral NSAID (excluding low-dose aspirin \[\<350 mg/day\]) or is taking daily oral nonsteroidal anti-inflammatory drug (NSAID) at greater than the maximum recommended dosage.
* Is currently on any chronic systemic (oral or IV) anti-infective therapy for chronic active infection (such as pneumocystis, cytomegalovirus, herpes zoster, or atypical mycobacteria).

Ages Eligible for Study: 18 Years to 75 Years (ADULT, OLDER_ADULT)

Sexes Eligible for Study: ALL

Accepts Healthy Volunteers: No

🗓️ Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

First Submitted 29 November 2023
First Submitted that Met QC Criteria 29 November 2023
First Posted 7 December 2023

Study Record Updates

Last Update Submitted that Met QC Criteria 26 July 2024
Last Update Posted 30 July 2024
Last Verified July 2024