The purpose of this study is to investigate the safety and tolerability of LY4298445 in healthy participants and in participants with systemic lupus erythematosus (SLE) or rheumatoid arthritis (RA). Participation in the study will last up to approximately 52 weeks.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
SINGLE
Enrollment
68
Nucleus Network
Brisbane, Australia
RECRUITINGNucleus Network
Melbourne, Australia
RECRUITINGPeking University First Hospital
Number of Participants with One or More Serious Adverse Event(s) (SAEs) Considered by the Investigator to be Related to Study Drug Administration
A summary of SAEs regardless of causality, will be reported in the Reported Adverse Events module
Time frame: Baseline up to Week 52
Pharmacokinetics (PK): Area Under the Concentration Versus Time Curve (AUC) of LY4298445
PK: AUC of LY4298445
Time frame: Baseline up to Approximately Week 57
PK: Maximum Concentration (Cmax) of LY4298445
PK: Cmax of LY4298445
Time frame: Baseline up to Week 52
Pharmacodynamic (PD): Degree of Peripheral B Cell Depletion Following Biopsy in Participants
PD: Peripheral B cell depletion
Time frame: Baseline up to Week 52
Trial questions or participation questions: 1-877-CTLILLY (1-877-285-4559)
CONTACT
Physicians interested in becoming principal investigators please contact
CONTACT
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Beijing, China
Peking University Third Hospital
Beijing, China
NOT_YET_RECRUITINGXiangya Hospital of Central South University
Changsha, China
NOT_YET_RECRUITINGAnhui Provincial Hospital
Hefei, China
NOT_YET_RECRUITINGRenji Hospital, Shanghai Jiaotong University School of Medicine
Shanghai, China
NOT_YET_RECRUITINGThe First Affiliated Hospital of Wenzhou Medical University
Wenzhou, China
NOT_YET_RECRUITINGUnion Hospital Tongji Medical College Huazhong University of Science and Technology
Wuhan, China
NOT_YET_RECRUITING