Drug Repurposing Programs - Opportunities and Best Practices

17 October 2024 | 14:00 - 15:15

Drug repurposing programs embody the potential to extend therapeutic application of an existing drug molecule to a novel indication, to aid patient groups that currently lack adequate or effective treatment. Developing an existing drug for a new indication may be a faster route to the clinic as well as a less cost-intensive approach, due to potentially suitability of existing clinical trial data in the registration process. Here, regularly faster and at lower cost compared to the R&D program for a new medicinal molecule.

In session 14 of the FIGON-Dutch Medicines Days, day 2, experts will share their insight knowledge on a series of aspects relevant for designing a successful repurposed drug program with a viable business case in mind, which are necessary to keep in mind in order to increase the odds of indeed finally making the drug available for patients in need thereof.  In session 14, light will shed on:

(1) clinical trial design for drug repurposing, 
(2) current and desired improved drug pricing- and reimbursement systems relating to drug repurposing, 
(3) pharmaceutical legislation of the European Union including proposed reform thereof in part in favour of drug repurposing programs, 
(4) registration requirements for a repurposed drug, 
(5) the benefits that patenting can provide for a drug repurposing program regarding staying in control when a pricing- and reimbursement scheme for example is established, and
(6) details of importance for an attractive drug repurposing program worthwhile for taking the risk to invest.

Chair: Barend Bouma (NLO)

Speakers: Bianca Pauly (3D-PharmXchange), Benien Vingerhoed (FAST), Jaap Mannaerts (NLO), Geert Corstens (Oost NL)

Abstract Presenters: TBA

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