Grade ≥ 3 AEs regardless of attribution to navoximod

Navoximod 50 mg BID (n = 1)Navoximod 100 mg BID (n = 3)Navoximod 200 mg BID (n = 3)Navoximod 400 mg BID (n = 3)Navoximod 600 mg BID (n = 3)Navoximod 800 mg BID (n = 6)All Patients 21/28 day schedule (N = 19)Navoximod continuous schedule 600 mg BID (n = 3)All Patients (N = 22)
Any adverse event1 (100%)3 (100%)1 (33%)3 (100%)2 (67%)2 (33%)12 (63%)2 (67%)14 (63%)
Neoplasm progression1 (33%)1 (33%)1 (33%)3 (16%)3 (14%)
AST increased1 (33%)1 (33%)2 (11%)2 (9%)
Anemia1 (33%)1 (5%)1 (5%)
Ascites1 (33%)1 (5%)1 (5%)
Dysphagia1 (33%)1 (5%)1 (5%)
Hypokalemia1 (17%)1 (5%)1 (5%)
Hypotension1 (17%)1 (5%)1 (5%)
Lower GI hemorrhage1 (17%)1 (5%)1 (5%)
Mental status changes1 (33%)1 (5%)1 (5%)
Muscular weakness1 (33%)1 (5%)1 (5%)
Peripheral neuropathy1 (33%)1 (5%)1 (5%)
Acute pancreatitis1 (33%)1 (5%)1 (5%)
Pneumonia1 (33%)1 (5%)1 (5%)
Small Intestinal Obstruction1 (33%)1 (5%)1 (5%)
Tumor pain1 (33%)1 (5%)1 (5%)
Bloody discharge1 (33%)1 (5%)
Diverticulitis1 (33%)1 (5%)
Lymphopenia1 (33%)1 (5%)