This study is researching an experimental drug called REGN7508 (called "study drug"). The study is focused on the prevention of Cancer-Associated Thrombosis (CAT) in participants. The aim of the study is to see how effective the study drug is in preventing blood clots in participants with solid tumors who are currently receiving anticancer treatment or planning to start anticancer treatment within a month of being assigned to a study treatment, or recovering from surgery, and how the study drug compares to placebo for CAT. The study is looking at several other research questions, including: * What side effects may happen from taking the study drug * How much study drug is in the blood at different times * Whether the body makes antibodies against the study drug (which could make the study drug less effective or could lead to side effects)
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
860
Administered per the protocol
Administered per the protocol
Time-to-first event of centrally adjudicated VTE [Deep Vein Thrombosis (DVT), non-fatal Pulmonary Embolism (PE) or Arterial thromboembolism (ATE), or thromboembolism- or ATE-related death]
Time frame: Through 6 months
Time-to-first event of centrally adjudicated International Society of Thrombosis and Hemostasis (ISTH) major bleeding or Clinically Relevant Non-Major (CRNM) bleeding
Time frame: Through 6 months
Time-to-first event of DVT (symptomatic or asymptomatic [proximal])
Time frame: Through 6 months
Time-to-first event of non-fatal PE (symptomatic or asymptomatic)
Time frame: Through 6 months
Time-to-first event of any ATE
Time frame: Through 6 months
Time-to-first event of thromboembolism- or ATE-related death
Time frame: Through 6 months
Occurrence of Treatment-Emergent Adverse Events (TEAEs)
Time frame: Up to day 245
Severity of TEAEs
Time frame: Up to day 245
Incidence of Anti-Drug Antibody (ADA) to REGN7508
Time frame: Up to day 245
Magnitude of ADA to REGN7508
Time frame: Up to day 245
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