Erasca (United States)

To pursue these therapeutic strategies, we are developing what we believe to be the deepest pipeline targeting multiple signaling nodes to shut down the RAS/MAPK pathway. Our approach is modality-agnostic, including small molecules, large molecules, and protein degraders—alone and in combinations across multiple tumor types— to selectively and potently inhibit or degrade critical in-pathway and escape-route signaling nodes of the RAS/MAPK pathway. We are a clinical-stage precision oncology compa

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To pursue these therapeutic strategies, we are developing what we believe to be the deepest pipeline targeting multiple signaling nodes to shut down the RAS/MAPK pathway. Our approach is modality-agnostic, including small molecules, large molecules, and protein degraders—alone and in combinations across multiple tumor types— to selectively and potently inhibit or degrade critical in-pathway and escape-route signaling nodes of the RAS/MAPK pathway. We are a clinical-stage precision oncology compa

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