Merus and Halozyme collaborate to advance subcutaneous Petosemtamab development
Merus has licensed Halozyme’s proprietary ENHANZE technology to develop and commercialize subcutaneous formulations of petosemtamab
Merus has licensed Halozyme’s proprietary ENHANZE technology to develop and commercialize subcutaneous formulations of petosemtamab
TLANDO was approved by the U.S. Food and Drug Administration (FDA) on March 28, 2022.
Subcutaneous nivolumab has potential to be the first and only subcutaneously administered PD-1 inhibitor
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