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Furthermore, this approach, creating a multispecific that is bivalent to the target and monovalent to the effector cell, results in a molecule with a mass similar to that of other multispecific antibodies that are already FDA-approved (e.g., Glofitamab) or still being evaluated in clinical trials (e.g., Imvotamab, an IgM-based bispecific)

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117-2), enacted on March 11, 2021 amended section 1886(d)(3)(E)(i) of the Act (42 U.S.C