AbbVie Announced That The U.S. FDA Has Approved EPKINLY As The First And Only T-cell Engaging Bispecific Antibody Administered Subcutaneously For The Treatment Of Adults With Relapsed Or Refractory Follicular Lymphoma
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AbbVie announced that the U.S. FDA has approved EPKINLY as the first and only T-cell engaging bispecific antibody administered subcutaneously for the treatment of adults with relapsed or refractory follicular lymphoma.
June 27, 2024 | 6:50 am
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AbbVie has received FDA approval for EPKINLY, a new treatment for relapsed or refractory follicular lymphoma. This approval marks a significant milestone as it is the first subcutaneous T-cell engaging bispecific antibody for this condition.
The FDA approval of EPKINLY is a significant milestone for AbbVie, as it introduces a novel treatment option for relapsed or refractory follicular lymphoma. This approval is likely to boost investor confidence and positively impact AbbVie's stock price in the short term.
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