Baird Global Healthcare Conference 2025
Logotype for Climb Bio Inc

Climb Bio (CLYM) Baird Global Healthcare Conference 2025 summary

Event summary combining transcript, slides, and related documents.

Logotype for Climb Bio Inc

Baird Global Healthcare Conference 2025 summary

8 Jul, 2026

Company overview and strategy

  • Focuses on developing monoclonal antibodies for high unmet need indications with clear regulatory paths and large commercial potential.

  • Lead program, Budoprutug (Budo), targets CD19 for B-cell-mediated diseases; second asset, CLYM116, targets APRO for IgA nephropathy.

  • Strategic indication selection is based on biological rationale, risk profiles, and commercial opportunities, grouped into three disease buckets: IgG4-mediated, single organ IgG1-3-mediated, and complex rheumatological diseases.

  • Emphasizes a data-driven approach to expand into additional indications based on initial study results.

  • Maintains a strong cash runway through 2027 to support multiple clinical milestones.

Lead asset (Budoprutug/Budo) development and differentiation

  • Budo is a CD19-targeting monoclonal antibody designed to deplete pathogenic B-cells while preserving protective immunity.

  • Offers both IV and subcutaneous formulations, with the latter showing high bioavailability, high concentration, and low viscosity in preclinical studies.

  • Subcutaneous dosing provides flexibility for patient and physician preferences, supporting broader adoption in community settings.

  • Differentiates from UPLINZA with higher CD19 affinity, unique Fc characteristics, and subcutaneous administration potential.

  • Dosing regimen allows for infrequent administration, aiming for disease-free intervals and improved patient experience.

Clinical development progress and trial designs

  • PMN (IgG4-mediated): Early data showed 60% complete renal response at 12 months and long-lived remissions after four doses; phase II study enrolling 45 patients in dose-escalation cohorts.

  • ITP (single organ): Targeting patients unresponsive to prior therapies; phase I/II study with dose escalation and up to one year follow-up for platelet response.

  • SLE (complex rheumatological): Early phase study with dose escalation in high CDI score patients, focusing on safety and efficacy as dose increases.

  • Data from these studies will guide further expansion within each disease bucket.

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