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NOT YET RECRUITING
NCT07564596
PHASE1/PHASE2

A Phase 1b/2a Study of Budoprutug in Systemic Lupus Erythematosus (SLE)

Sponsor: Climb Bio, Inc.

View on ClinicalTrials.gov

Summary

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.

Official title: A Phase 1b/2a Open-Label, Dose-Escalation and Dose-Expansion Study to Evaluate Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Budoprutug (TNT119) in Adult Subjects With Systemic Lupus Erythematosus (SLE)

Key Details

Gender

All

Age Range

18 Years - 65 Years

Study Type

INTERVENTIONAL

Enrollment

30

Start Date

2026-06

Completion Date

2027-09

Last Updated

2026-05-04

Healthy Volunteers

No

Interventions

DRUG

Budoprutug

Single IV dose of study product on Day 1 and Day 15

Locations (1)

Peking University People's Hospital

Beijing, China