LY4298445
DrugAdministered SC
NCT Number: NCT07276958
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.
Interested in participating?
Request Info18 year–55 year
All sexes
Interventional
Phase 1
Nucleus Network, Brisbane, Australia
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Healthy Participants
Healthy participants between the ages of 18 and 55 years.
Participants with Systemic Lupus Erythematosus (SLE)
Participants with Rheumatoid Arthritis (RA)
Exclusion criteria
Administered SC
Time frame: Baseline up to Week 52
A summary of SAEs regardless of causality, will be reported in the Reported Adverse Events module
Time frame: Baseline up to Approximately Week 57
PK: AUC of LY4298445
Time frame: Baseline up to Week 52
PK: Cmax of LY4298445
Time frame: Baseline up to Week 52
PD: Peripheral B cell depletion
Contact information is provided by the study sponsor or research team.
Physicians interested in becoming principal investigators please contact
CONTACT
Trial questions or participation questions: 1-877-CTLILLY (1-877-285-4559)
CONTACT
Eli Lilly and Company
Industry
A Phase 1, Multicenter, Randomized, Placebo-Controlled, Participant-Blind, Single-Ascending Dose Study of LY4298445 in Healthy Participants and an Open-Label Single-Ascending Dose and Multiple-Ascending Dose Study of LY4298445 in Participants With Systemic Lupus Erythematosus or Rheumatoid Arthritis
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.
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