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Musings from The Power List: Miguel Forte
Scientific progress alone isn't enough, says Miguel Forte, who argues that reimbursement and patient access will shape the next decade of cell and gene therapy
Miguel Forte serves as President of ISCT, focusing on enhancing the society's global presence and establishing its clinical pillar.
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Patient access is currently the greatest challenge in cell and gene therapy, hindered by manufacturing capacity, clinical delivery, and reimbursement issues.
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Allogeneic cell therapies, especially those from induced pluripotent stem cells, are making significant progress but lack sufficient attention.
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Faster clinical trial approvals and pragmatic health technology assessments are essential for accelerating progress in cell and gene therapy.
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The integration of improved gene editing and AI is expected to transform drug development, making it more proactive and design-oriented.
A first-in-human study reduces stem-cell collection and manufacturing times, Bristol Myers ends its Breyanzi agreement with Cellares, and two approaches strengthen CAR T-cell activity against solid tumors