CGT Space Faces Some Challenges, but There ‘Still Is a Place’ for Therapies

  • Mar 13, 2025

    The cell and gene therapy (CGT) space seems to be a bit of a mixed bag recently. While last year’s accomplishments included FDA approvals of two new first-in-class treatments for solid tumors and the first chimeric antigen receptor T cell (CAR-T) therapy since 2022, on back-to-back days last month, the news was more downbeat.

    On Feb. 20, reports that Pfizer Inc. was discontinuing its hemophilia B gene therapy Beqvez (fidanacogene elaparvovec) globally were first publicized and later confirmed by the drugmaker. The FDA had approved the single-dose $3.5 million treatment less than a year prior, on April 25, 2024.

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  • Angela Maas

    Angela has an extensive background of editing, reporting and writing for trade and consumer publications. She has written Radar on Specialty Pharmacy since she joined AIS Health in 2005 and has broad knowledge of the various issues at play within the space. She also has written for Spotlight on Market Access since its 2017 launch. Before joining AIS Health, she was managing editor at Employee Benefit News and Employee Benefit News Canada and managing editor at Hem Aware (a hemophilia publication), Lupus Living and Momentum (a multiple sclerosis publication). She has a B.A. in English and an M.A. in British literature from Arizona State University.

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