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Alentis Therapeutics: Alentis Receives FDA Orphan Drug Designation for Lixudebart to Treat Idiopathic Pulmonary Fibrosis

Alentis Therapeutics Doses First ANCA-Associated Vasculitis Rapidly Progressive Glomerulonephritis Patient in Phase 2 Clinical Trial of Lixudebart (ALE F02)

Alentis Therapeutics Doses First ANCA-Associated Vasculitis Rapidly Progressive Glomerulonephritis Patient in Phase 2 Clinical Trial of Lixudebart (ALE F02)
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Alentis Therapeutics Doses First Patient in Phase 1/2 Clinical Trial of ALE C04 in Head and Neck Squamous Cell Carcinoma (HNSCC)

Alentis Therapeutics Doses First Patient in Phase 1/2 Clinical Trial of ALE C04 in Head and Neck Squamous Cell Carcinoma (HNSCC)
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Alentis Therapeutics Appoints Lung Experts Professors Tony Mok and Steven Nathan to its Scientific Advisory Board

Alentis Therapeutics Appoints Lung Experts Professors Tony Mok and Steven Nathan to its Scientific Advisory Board
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Alentis Therapeutics Appoints Lung Experts Professors Tony Mok and Steven Nathan to its Scientific A

BASEL, Switzerland (BUSINESS WIRE) #CLDN1 Alentis Therapeutics (“Alentis”), the clinical-stage biotechnology company developing treatments for Claudin-1 positive (CLDN1+) tumors and organ fibrosis, announced today the appointment of Tony Mok, Professor of Clinical Oncology at the Chinese University of Hong Kong a.

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