PRodrug technology for Immunotherapy-priming via patient-friendly at-home MEtronomic dosing

Información del proyecto

PRIME

Identificador del acuerdo de subvención: 101138100

DOI

10.3030/101138100

Proyecto cerrado

Fecha de la firma de la CE 28 Septiembre 2023

Fecha de inicio 1 Octubre 2023

Fecha de finalización 31 Marzo 2025

Financiado con arreglo a

• European Research Council (ERC)

Coste total

Sin datos

Aportación de la UE

€ 150 000,00

Coordinado por

UNIVERSITAETSKLINIKUM AACHEN
Germany

Periodic Reporting for period 1 - PRIME (PRodrug technology for Immunotherapy-priming via patient-friendly at-home MEtronomic dosing)

Período documentado: 2023-10-01 hasta 2025-03-31

Resumen del contexto y de los objetivos generales del proyecto

The PRIME project aimed to overcome the challenges associated with traditional chemo- and immunotherapy approaches and make those more accessible and effective. The main objectives of the project were to assess the technical and commercial feasibility of a modular prodrug technology to enable at-home metronomic dosing of immunogenic drugs for cancer immunotherapy. To this end, we set out to establish a synthetic and formulation strategy to produce a more tolerable immunogenic prodrug platform. Furthermore, we aimed to develop injectable formulations of the prodrugs, and we evaluated the prodrug performance in combination with immunotherapy at different doses in preclinical models. Finally, we also explored the feasibility of different routes of administration (intravenous vs. subcutaneous) of injectable (nano-)formulations, as well as screened competitors’ landscape and explored market opportunities for future commercialization.

Trabajo realizado desde el comienzo del proyecto hasta el final del período abarcado por el informe y los principales resultados hasta la fecha

In order to explore the innovation potential of our prodrug platform technology, and pave the way towards industrial development and commercialization, we aimed to test, optimize, assess and validate the prodrug technology at two levels in parallel: technical and commercial. In brief, at the technical level our activities were focused on the following key aspects: technical and preclinical validation, including synthesis, formulation, tolerability and efficacy assessment in terms of immuno-priming. This also included proof-of-concept of administration feasibility and targeting via different routes of administration, including subcutaneous. Additionally, we also explored further intellectual property foreground and the best route(s) to market, including a clinical and market landscape assessment, as well as potential partner identification.

Avances que van más allá del estado de la técnica e impacto potencial esperado (incluida la repercusión socioeconómica y las implicaciones sociales más amplias del proyecto hasta la fecha)

We have assessed the technical and commercial feasibility of a modular immuno-priming prodrug platform technology for cancer immunotherapy.

At the technical level, we have successfully (i) optimized the synthetic strategy of the prodrug platform, increasing production rate via implementing semi-automatic purification chromatographic methods. We have also (ii) developed injectable formulations to enable safe administration of the prodrug platform in vivo, coupled to both doxorubicin and gemcitabine, as proof-of-concept immunogenic chemotherapeutic drugs, thus showing the versatility and applicability of the platform technology. The different immunogenic prodrugs were effectively formulated in both clinically relevant Cremophor-based solubilizing agents, and into biocompatible, proprietary PEGylated HPMA-based polymeric micelles, resulting in stable injectable formulations. Furthermore, we (iii) have extensively evaluated the preclinical performance of the doxorubicin-based immunogenic prodrug, formulated in Cremophor and into the polymeric micelles, and applied as monotherapy and in combination with immune checkpoint inhibitors in orthotopic and syngeneic breast cancer mouse models. This also included a first evaluation of the feasibility for subcutaneous (pro)drug administration in vivo using the proprietary polymeric micelle formulation, which confirmed efficient targeting of and drug delivery into tumors and lymph nodes, thereby opening opportunities for further research into developing an at-home subcutaneously administrable product for cancer immunotherapy.

At the commercial level, we have (iv) refined the IP landscape, and started preparing foreground IP for the newly developed prodrugs (gemcitabine- and oxalipatin-prodrugs). Finally, together with the help of a consulting company specialized in grants and innovation, we have (v) focused on analyzing the immuno-oncology and immuno-priming clinical and market landscape, including carrying out several interviews to key opinion leaders in the fields of immuno-oncology, as well as to experts in regulatory and drug pricing aspects. Together, this has allowed us to set a plan for further technology transfer evaluation (with the RWTH innovation office) and eventual incorporation of our prodrug platform in clinical trials regimens (with the Center for Translational & Clinical Research, CTCA, in Aachen), as well as towards future commercialization of a potential product based on our platform technology.