Climb Bio, Inc. ((CLYM)) announced an update on their ongoing clinical study.
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Study Overview: Climb Bio, Inc. is conducting a Phase 1b/2a study titled A Phase 1b/2a, Open-Label, Sequential-Cohort, Dose Escalation and Expansion Study to Evaluate Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Preliminary Clinical Effectiveness of Budoprutug (TNT119) in Subjects With Immune Thrombocytopenia (ITP). The study aims to assess the safety and tolerability of Budoprutug in adults with ITP, along with its pharmacokinetics, pharmacodynamics, and preliminary clinical effectiveness.
Intervention/Treatment: The study tests Budoprutug, a drug administered as a single intravenous dose on Day 1 and Day 15. The treatment aims to improve the condition of patients with Immune Thrombocytopenia by targeting specific biological pathways.
Study Design: This is a non-randomized, open-label study with a sequential intervention model. Participants are enrolled in three dose-escalating cohorts, followed by an expansion cohort. The primary purpose is treatment, and there is no masking involved.
Study Timeline: The study began on June 20, 2025, with primary completion expected shortly thereafter. The last update was submitted on October 20, 2025. These dates are crucial for tracking the study’s progress and anticipating results.
Market Implications: The ongoing study could significantly impact Climb Bio’s stock performance and investor sentiment, particularly if Budoprutug shows promising results. Success in this trial may position Climb Bio favorably against competitors in the biologics and monoclonal antibody market, potentially leading to increased investor interest.
The study is currently recruiting, with further details available on the ClinicalTrials portal.