Savara resubmits FDA application for potential treatment in rare lung disease patients
The resubmission of BLA for MOLBREEVI names Fujifilm as the drug substance manufacturer
The resubmission of BLA for MOLBREEVI names Fujifilm as the drug substance manufacturer
Efdoralprin alfa, a recombinant human alpha-1 antitrypsin (AAT)-Fc fusion protein, showed superior efficacy to standard plasma-derived therapy in adults with AATD
This partnership aims to embed latest technological advancements in diagnosing and managing lung disorders and associated non-communicable diseases like asthma, pulmonary fibrosis and COPD.
The study found that nerandomilast effectively slowed lung function decline in patients, with discontinuation rates similar to placebo
Efdoralprin Alfa was well tolerated, with a safety profile comparable to plasma-derived therapy
New gene expression profiling test enhances precision in assessing lung transplant rejection and injury
Funding supports development of first-in-class pan-ROCK inhibitor ROC-101 through Phase 2a clinical testing
FDA grants accelerated approval to zongertinib for HER2 TKD-Mutated Non-Squamous NSCLC
AstraZeneca and Daiichi Sankyo’s Enhertu followed by THP showed an improved safety profile vs. standard of care
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