Impact of fast-track regulatory designations on strategic commercialization decisions for autologous cell therapies

Author:

Lam Ching1ORCID,Meinert Edward234ORCID,Yang Aidong5ORCID,Cui Zhanfeng1ORCID

Affiliation:

1. Department of Engineering Science, Institute of Biomedical Engineering, University of Oxford, Oxford, OX3 7DQ, UK

2. Centre for Health Technology, University of Plymouth, Plymouth, UK

3. Department of Primary Care and Public Health, Imperial College London, London, UK

4. Harvard T.H. Chan School of Public Health, Harvard University, Boston, MA, USA

5. Department of Engineering Science, University of Oxford, Oxford, OX1 3PJ, UK

Abstract

Background: Regulatory authorities around the world have introduced incentives to improve the speed-to-market of innovative therapies. Aim & methods: To better understand the capacity and portfolio planning decisions of autologous cell therapies and particularly the impact of fast-tracking designations, this paper describes a mixed-integer linear programming approach for the optimization of capacity investment and portfolio selection decisions to maximize the net present value of a candidate portfolio of therapies under different regulatory programs. Results: The illustrative example shows that fast-track designations allow a 25% earlier breakeven, 42–86% higher net present value over a 20-year horizon with earlier upfront capital and reduce the portfolio’s sensitivity to uncertainties. Conclusion: Fast-track designations are effective in providing commercialization incentives, but high capital risks given the compressed timeline should be better considered.

Publisher

Future Medicine Ltd

Subject

Embryology,Biomedical Engineering

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