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Description

Idiopathic Pulmonary Fibrosis (IPF) is a chronic and progressive interstitial lung disease characterized by damage to lung architecture, resulting in an irreversible loss of function

99% COA supported RUO CAS 2375614-45-8 Molecular weight 3962.4 g/mol Storage -20C recommended (research-only) Package sizes 1 5 mg vial Description Cagrilintide 5 mg research overview Cagrilintide amylin analogue for metabolic and satiety-pathway research