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Publications & Presentations

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Rademikibart - Dermatology
Rademikibart - Respiratory
Rapid and Sustained FEV1 improvements with Rademikibart in Type 2 Asthma: Impact of Eosinophils and FeNO

Presented at the 2025 European Respiratory Society (ERS) Congress,  September 27 to Oct 1, 2025

Rademikibart in Moderate-to-Severe Asthma: Impact of Eosinophils and Regional Differences on Response

Presented at the 2025 European Respiratory Society (ERS) Congress,  September 27 to Oct 1, 2025

Reduction in Annualized Exacerbations with Rademikibart in Eosinophilic-driven Type 2 Asthma

Presented at the 2025 European Association of Allergy and Clinical Immunology (EAACI) Congress, June 13 to 16, 2025 

Improvement in Lung Function with Rademikibart in Eosinophilic-driven Type 2 Asthma

Presented at the 2025 European Association of Allergy and Clinical Immunology (EAACI) Congress, June 13 to 16, 2025 

Optimized Second-generation IL-4Rα Inhibition: Structural and Molecular Dynamics Properties of the Rademikibart Fab-IL-4Rα Complex

Presented at the American Thoracic Society (ATS) Congress, May 16-21, 2025

Effect of Rademikibart on Blood Eosinophil Counts in Patients with Asthma: Is there an IL-4Rα Class Effect?

Presented at the American Thoracic Society (ATS) Congress, May 16-21, 2025

Rapid Improvement in Lung Function Observed with Rademikibart in Patients with Moderate-to-Severe Uncontrolled Asthma

Presented at the American Thoracic Society (ATS) Congress, May 16-21, 2025

Efficacy of Rademikibart in COPD-like Patients: Sub-analyses from the Phase 2b Trial in Patients with Moderate-to-Severe Asthma

Presented at the American Thoracic Society (ATS) Congress, May 16-21, 2025

Improved lung function and asthma control observed with rademikibart in patients with moderate-to-severe asthma

Oral presentation at the European Respiratory Society (ERS) Congress, September 7-11, 2024

Improved Lung Function and Asthma Control Observed with Rademikibart in Patients with Moderate-to-Severe Uncontrolled Asthma (CBP-201-WW002)

Presented at the American Thoracic Society (ATS) Congress, May 17-22, 2024

Rademikibart - Dermatology
Optimized Second-Generation IL-4Rα Inhibition: Structural and Molecular Dynamics Properties of Rademikibart Fab-IL-4Rα Complex

Presented at the 44th Annual Fall Clinical (FC) Dermatology Conference, October 24-27, 2024

Rademikibart (IL-4RαBlocker) Integrated Exposure-Response Analysis Supports Differentiated Once Monthly Dosing Regimen

Presented at the European Academy of Dermatology and Venereology Congress (EADV), September 25-28, 2024

Maintenance of Investigator and Patient Reported Outcomes over 52 Weeks were Observed with Rademikibart in Patients with Moderate-to-Severe Atopic Dermatitis (SEASIDE CHINA)

Presented at the European Academy of Dermatology and Venereology Congress (EADV), September 25-28, 2024

Continued Improvement of Investigator and Patient Reported Outcomes into the 52-Week Maintenance Period were Observed with Rademikibart in Patients with Moderate-to-Severe Atopic Dermatitis (SEASIDE CHINA)

Presented at the European Academy of Dermatology and Venereology Congress (EADV), September 25-28, 2024

Positive 52-Week Maintenance Data Observed with Rademikibart in Patients with Moderate-to-Severe Atopic Dermatitis - SEASIDE CHINA

Presented at the Revolutionizing Atopic Dermatitis (RAD 2024) Conference, June 8-10, 2024

Rademikibart (CBP-201) a next-generation IL-4Rα antibody, achieved all primary and secondary endpoints in a randomized pivotal trial for moderate-to-severe atopic dermatitis (AD) in China 

Presented at the World Congress of Dermatology (WCD), July 3-8, 2023

Eczema Area and Severity Index (EASI) scores improved, and encouraging safety and tolerability were observed, across 16 weeks of treatment with rademikibart (CBP-201) for moderate-to-severe  atopic dermatitis (AD) A pivotal trial in China (CBP-201-CN002)

Presented at the World Congress of Dermatology (WCD), July 3-8, 2023

Improvements in investigator-rated outcomes across 16 weeks of treatment with rademikibart (CBP-201) for moderate-to-severe atopic dermatitis (AD): Results from a pivotal trial in China (CBP-201-CN002)

Presented at the World Congress of Dermatology (WCD), July 3-8, 2023

Improvements in patient-reported outcomes (PROs) across 16 weeks of treatment with rademikibart (CBP-201) for moderate-to-severe atopic dermatitis (AD): Results from a pivotal trial in China 

Presented at the World Congress of Dermatology (WCD), July 3-8, 2023

Potentially Greater Efficacy with CBP-201 for Adults with Severe versus Moderate Atopic Dermatitis at Baseline: Subgroup Analyses from the WW001 Phase 2 Randomized Trial

Presented at the Revolutionizing Atopic Dermatitis (RAD) Conference, April 30, 2023

CBP-201, a next-generation IL-4Rα antibody, achieved all primary and secondary efficacy endpoints in the treatment of adults with moderate-to-severe atopic dermatitis (AD): A randomized, double-blind, pivotal trial in China (CBP-201-CN002)

Presented at the American Academy of Dermatology (AAD) Annual Meeting, March 17-21, 2023

Rapid and Sustained Improvements with CBP-201 Across All Body Regions: Treatment of Atopic Dermatitis in a Phase 2b, Randomized, Double-blind, Placebo-controlled Trial (CBP-201-WW001)

Presented at the American Academy of Dermatology (AAD) Annual Meeting, March 17-21, 2023

CBP-201: A Next Generation IL-4Rα Blocker

Oral presentation at the 6th Annual Dermatology Drug Development Summit (DDDS), November 1–3, 2022

Investigator-Rated Efficacy Outcomes Across 16 Weeks of Treatment with CBP-201: Results from a Phase 2b Trial in Patients with Atopic Dermatitis (CBP-201-WW001)

Presented at the 31st European Academy of Dermatology and Venereology Congress (EADV), September 7-10, 2022

Patient-Reported Efficacy Outcomes Across 16 Weeks of Treatment with CBP- 201: Results from a Phase 2b Trial in Patients with Atopic Dermatitis (CBP-201- WW001)

Presented at the 31st European Academy of Dermatology and Venereology Congress (EADV), September 7-10, 2022

CBP-201, a novel and differentiated IL-4Rα targeting antibody being evaluated in Th2 inflammatory diseases

Presented at the Society for Investigative Dermatology (SID) Annual Meeting, May 18-21, 2022

Disease Control and Quality of Life: Efficacy Outcomes from the Phase 2b Trial of CBP-201 in Patients with Atopic Dermatitis (CBP-201-WW001)

Presented at the Revolutionizing Atopic Dermatitis (RAD) Conference, April 9 - 11, 2022

Efficacy and Safety of CBP-201 in Adults with Moderate-to-Severe Atopic Dermatitis (AD): A Phase 2b, Randomized, Double-blind, Placebo-controlled Trial (CBP-201-WW001)

Presented at the Maui Derm Conference, January 24, 2022

The Effect of Baseline Disease Characteristics on Efficacy Outcomes: Results from a Phase 2b, Randomized, Double-blind, Placebo-controlled Trial of CBP-201 in Adults with Moderate-to-Severe Atopic Dermatitis (AD)

Presented at the Maui Derm Conference, January 24, 2022

A randomized, double-blind, placebo-controlled, multiple ascending dose study of the safety, pharmacokinetics and preliminary efficacy of CBP-201 in adult patients with moderate to severe atopic dermatitis (CPB-201AU002)

Presented at the 29th European Academy of Dermatology and Venereology Congress (EADV), October 29, 2020

Icanbelimod – Ulcerative Colitis (UC)
The Effect of Baseline Disease Characteristics on Efficacy Outcomes: Results from a Phase 2b, Randomized, Double-Efficacy and safety of icanbelimod (CBP-307) in adults with moderate-to-severe ulcerative colitis: A phase 2, randomized, double-blind, placebo-controlled trial, Placebo-controlled Trial of CBP-201 in Adults with Moderate-to-Severe Atopic Dermatitis (AD)

Presented at the Advances in Inflammatory Bowel Diseases, December 14-16, 2023

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