Table 1.
Drug | Disease | Trials* | Primary Pathway(s) Targeted |
---|---|---|---|
Nintedanib | IPF | Tomorrow INPULSIS 1, 2 | VEGF, FGF, PDGF |
Nintedanib | LAM | Nintedanib for LAM (phase II) | PDGF, FGF, VEGF |
Imatinib | PAH | IMPRES | PDGF, c-KIT |
Imatinib | LAM | LAMP-1 | VEGF |
Imatinib | IPF | Gleevec IPF Study | PDGF |
Imatinib | Asthma | KIA | c-KIT |
Dasatinib | IPF | Targeting proinflammatory cells in IPF | Src |
Sorafenib | PAH | Dosing in patients with PAH (phase I) | VEGF, Raf-1 kinase |
Sorafenib | Hepatopulmonary syndrome | SHPS (phase II) | VEGF |
Saracatinib | LAM | SLAM-1 | Src |
Definition of abbreviations: FGF = fibroblast growth factor; IMPRES = Imatinib (QTI571) in Pulmonary Arterial Hypertension study; IPF = idiopathic pulmonary fibrosis; KIA = Effects of c-Kit Inhibition by Imatinib in Patients with Severe Refractory Asthma study; LAM = lymphangioleiomyomatosis; LAMP-1 = LAM Pilot Study with Imatinib Mesylate 1; PAH = pulmonary arterial hypertension; PDGF = platelet-derived growth factor; SHPS = Sorafenib for Hepatopulmonary Syndrome; SLAM-1 = Tolerability of Saracatinib in Subjects with Lymphangioleiomyomatosis; VEGF = vascular endothelial growth factor.
Cancer trials excluded (see www.clinicaltrials.gov).