A Phase 1b/2a Study of Budoprutug in Systemic Lupus Erythematosus (SLE)
Sponsor: Climb Bio, Inc. • ClinicalTrials.gov ID: NCT07564596
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Budoprutug is a humanized, immunoglobulin (Ig) G1 monoclonal antibody that selectively binds to CD19 and is projected to deplete targeted cells through antibody-dependent cellular cytotoxicity. This Phase 1b/2a, open-label study will evaluate budoprutug in ascending dose cohorts of patients aged 18 years and above with active, seropositive SLE and inadequate response to standard therapy. The study will also assess the pharmacokinetics, pharmacodynamics and early indications of efficacy of budoprutug in SLE, where pharmacodynamics will be evaluated as the change in the number of B cells and immunoglobulins (antibodies) in the blood over time. Budoprutug will be administered as two (2) IV infusions 14 days apart in ascending dose cohorts.
Interventions
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Budoprutug
(Drug)
Single IV dose of study product on Day 1 and Day 15
Eligibility criteria
Conditions
Locations
- Mianyang Central Hospital — Mianyang, Sichuan, China
- Baoji Central Hospital — Baoji, China
- Peking University People's Hospital — Beijing, China
- The First Affiliated Hospital of Bengbu Medical College — Bengbu, China
- Xiangya Second Hospital of Central South University — Changsha, China
- The First Affiliated Hospital of the University of Science — Hefei, China
- The First Affiliated Hospital of Nanchang — Nanchang, China
- The Second Affiliated Hospital of Soochow University — Suzhou, China
- Shanxi Bethune Hospital — Taiyuan, China
- Zaozhuang Municipal Hospital — Zaozhuang, China
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Data sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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