Mosunetuzumab
DrugParticipants will receive SC mosunetuzumab.
NCT Number: NCT07598396
This study will assess how mosunetuzumab works in people who have systemic lupus erythematosus (SLE) who may or may not also have active lupus nephritis (LN).
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Phase 2
Clnica SER da Bahia, Salvador, Estado de Bahia, Brazil
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Participants will receive SC mosunetuzumab.
Time frame: Up to Week 76
Drug-Free Remission is defined as achieving both of the following: Absence of disease activity maintained for 6 months after completion of mosunetuzumab treatment, and; not receiving any SLE-directed therapy (except for antimalarials) during the 6 months. Doses of prednisone (or equivalent) ≤5 mg/day to treat secondary adrenal insufficiency are permitted.
Time frame: Up to Week 76
DORIS remission is defined as achievement of all of the following for at least 6 months: Clinical systemic lupus erythematosus disease activity index (cSLEDAI) = 0 after completion of mosunetuzumab treatment; stable dosing of SLE therapies for at least 6 months; Physician Global Assessment (PGA) of < 0.5, and; prednisone (or equivalent) dose ≤5 mg/day.
Time frame: Weeks 24, 52, 76, and 104
CRR is defined as all of the following: Urinary protein-to-creatinine ratio (UPCR) < 0.5 g/g, and; estimated glomerular filtration rate (eGFR) ≥ 85% of baseline, as calculated using the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equation or ≥ 60 ml/min per 1.73 m^2 of body-surface area.
Time frame: Weeks 24, 52, 76, and 104
PRR is defined as all of the following: ≥ 50% reduction in UPCR from baseline; UPCR < 1 g/g (or < 3 g/g if the baseline UPCR was ≥ 3 g/g), and; eGFR ≥85% of baseline, as calculated using the CKD-EPI equation.
Time frame: Up to 2.5 years
Time frame: Up to 2.5 years
Time frame: Up to 2.5 years
Time frame: Up to 2.5 years
Time frame: Baseline up to 2.5 years
Time frame: Up to 2.5 years
Time frame: Baseline to Week 76
Time frame: Baseline to Week 76
Contact information is provided by the study sponsor or research team.
Fastest response: use the inquiry form. https://www.gene.com/contact-us/submit-medical-inquiry
CONTACT
Reference Study ID Number: GA45799 https://forpatients.roche.com/ No attachments to email below.
CONTACT
888-662-6728 (U.S. Only)
Hoffmann-La Roche
Industry
A Phase II Open-Label Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of Mosunetuzumab in Patients With Systemic Lupus Erythematosus With or Without Active Lupus Nephritis
Acronym: SOLUNA
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT06434363
Autoimmune Diseases, Autoimmune Disorders
Houston, Texas, United States
View Trial DetailsNCT07107659
Autoimmune Diseases, Connective Tissue Diseases
New York, United States
View Trial DetailsNCT06839976
Autoimmune Diseases, CAR T Cell
Philadelphia, Pennsylvania, United States
View Trial DetailsNCT06737380
Autoimmune Diseases, Connective Tissue Diseases
Charleston, South Carolina, United States
View Trial Details