China Economic Observer Network: Cedars Medical (CLDX.US) announced its key R&D plans for 2026, focusing on progress in multiple clinical trials and platform validation.
Company Project Progress
CSU Phase III Clinical Trial: The Phase III study of the main drug Barzol for chronic spontaneous urticaria (CSU) is expected to complete patient enrollment by July 2026. The release of this data is the management’s most anticipated event.
Product Development Progress
Phase II Data Readout: Results from Phase II studies on nodular prurigo and atopic dermatitis are planned to be announced in 2026. These studies will be used to determine dosing regimens for subsequent registration trials.
Company Project Progress
Bispecific CDX622 Data Update: Data from the multiple-dose escalation study is expected to be released in Q3 2026. Results from the subcutaneous single-dose escalation study are also planned to be announced within 2026. The company plans to initiate mechanism validation studies for severe asthma based on these data.
Company Project Progress
New Indication Expansion Assessment: The company will start evaluating the potential to expand Barzol into new indications such as food allergies and allergic rhinitis.
Strategic Progress
Mid- to Long-term Strategic Focus: The company is committed to validating its bispecific platform (CDX622) and promoting Barzol to become the preferred drug for diseases like CSU. In terms of commercialization, it plans to independently advance in the U.S. market and seek partners outside the U.S.
The above information is compiled from public sources and does not constitute investment advice.
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Cedes Medical Announces 2026 R&D Milestones, Barzol Drug Phase III Trial Becomes Focus
China Economic Observer Network: Cedars Medical (CLDX.US) announced its key R&D plans for 2026, focusing on progress in multiple clinical trials and platform validation.
Company Project Progress
CSU Phase III Clinical Trial: The Phase III study of the main drug Barzol for chronic spontaneous urticaria (CSU) is expected to complete patient enrollment by July 2026. The release of this data is the management’s most anticipated event.
Product Development Progress
Phase II Data Readout: Results from Phase II studies on nodular prurigo and atopic dermatitis are planned to be announced in 2026. These studies will be used to determine dosing regimens for subsequent registration trials.
Company Project Progress
Bispecific CDX622 Data Update: Data from the multiple-dose escalation study is expected to be released in Q3 2026. Results from the subcutaneous single-dose escalation study are also planned to be announced within 2026. The company plans to initiate mechanism validation studies for severe asthma based on these data.
Company Project Progress
New Indication Expansion Assessment: The company will start evaluating the potential to expand Barzol into new indications such as food allergies and allergic rhinitis.
Strategic Progress
Mid- to Long-term Strategic Focus: The company is committed to validating its bispecific platform (CDX622) and promoting Barzol to become the preferred drug for diseases like CSU. In terms of commercialization, it plans to independently advance in the U.S. market and seek partners outside the U.S.
The above information is compiled from public sources and does not constitute investment advice.