Climb Bio reports early PrisMN Phase 2 data for budoprutug in kidney disease
Low-dose budoprutug showed B-cell depletion and immunologic remission at Week 12, with additional Phase 2 data expected in 2027.
Climb Bio, Inc. announced on October 24, 2026 new clinical data for budoprutug, its anti-CD19 monoclonal antibody, in primary membranous nephropathy (pMN) and minimal change disease (MCD), presented at American Society of Nephrology (ASN) Kidney Week 2026 in Denver, held October 21-25, 2026.
PrisMN is a Phase 2 dose-escalation study testing budoprutug at 200 mg, 600 mg, and 1000 mg in patients with moderate to severe pMN.1 Enrolled patients had already received prior treatment and showed high proteinuria and elevated PLA2R antibody levels at the start of the study.1
In the 200 mg cohort, the mean PLA2R antibody reduction was 70% at Week 12, and five of 13 patients (38%) achieved immunologic remission.1 Among patients whose baseline PLA2R antibody readings were under 175 RU/mL, the average reduction reached 80% by Week 12.1 The company said these Phase 2 Week 12 results in the 200 mg group matched earlier Phase 1b findings across B-cell depletion, antibody reduction, and remission rate.1
Early results from the 600 mg cohort pointed to greater drug exposure and deeper peripheral B-cell depletion compared with 200 mg.1 Mean peripheral CD20+ B-cell suppression at Week 4 reached 98% in the 600 mg group versus 74% at 200 mg, and a population pharmacokinetic analysis across roughly 120 patients found that those with high proteinuria cleared the drug at least twice as fast as non-proteinuric patients, supporting testing of higher doses.1
On safety, the company reported budoprutug was generally tolerated well across the two cohorts, with follow-up data spanning 12 weeks for the 200 mg group and 6 weeks for the 600 mg group; most adverse events were mild to moderate, and no treatment-related serious adverse events, discontinuations, or deaths were recorded.1 Enrollment in the 1000 mg cohort continues, and the company expects to report further PrisMN Phase 2 results in 2027.1
Separately, a case study described one MCD patient who received 100 mg of budoprutug and experienced three years of steroid-free remission, remaining in remission for a year after B-cell levels recovered.1
Written by readthrough’s AI from the linked primary sources and fact-checked against them automatically before publishing. Not investment advice.