ACT Brief: Lilly Seeks FDA Priority Review for Oral GLP-1 as Bispecific Antibody Trials Redefine Ethical Standards | Applied Clinical Trials Online

ACT Brief: Lilly Seeks FDA Priority Review

Eli Lilly's orforglipron may become the first oral GLP-1 therapy reviewed under FDA's new national priority program.

Bispecific antibody research in oncology is redefining ethical standards, with the global BsAb market projected to quadruple by 2030.

Emerging Regulatory Frameworks

The global BsAb market is projected to quadruple by 2030.

Author's summary: Lilly seeks FDA review for oral GLP-1 therapy.

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Applied Clinical Trials Online Applied Clinical Trials Online — 2025-11-03

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