PEPTO1
Financiado
Feasibility study of a novel treatment for cancer based on a recombinant peptide...
Peptomyc S.L. is an SME created to develop a new, first-in-class, cancer therapy using innovative anti-Myc peptides. Myc is an oncogene deregulated in the majority of human cancers, making Peptomyc’s products potentially applicabl...
Peptomyc S.L. is an SME created to develop a new, first-in-class, cancer therapy using innovative anti-Myc peptides. Myc is an oncogene deregulated in the majority of human cancers, making Peptomyc’s products potentially applicable to all cancer patients. The recombinant peptides are based on Omomyc, a Myc inhibitor benefiting from 20 years of preclinical validation as gene therapy. Omomyc displays remarkable therapeutic impact in multiple cancer models, with limited side effects, and no emergence of resistance. These peptides (Omomyc-CPP) developed by Peptomyc have unexpected cell-penetrating properties that make them excellent candidates for drug development. Three different drug products are being derived from the same drug substance, based on different administration routes, formulations and delivery devices. Peptomyc’s first mission is to take the first drug product (OMO-101) to completion of a successful phase I/II clinical trial, demonstrating safety and efficacy initially in glioblastoma (GBM) patients. Upon completion of phase I/II, Peptomyc plans to reach a licensing deal with a pharmaceutical company, to take care of further development and commercialization of OMO-101. In the feasibility study proposed here, Peptomyc’s team will elaborate and refine the business development plan of this new therapy to maximize its social and commercial potential. Such study will include:
a. Management of the IPR strategy;
b. Selection of the best CRO partners for [1] execution of safety studies, [2] clinical trials coordination, [3] Pre-IND and IND applications and other regulatory requirements;
c. EMA Briefing meeting;
d. Refinement of the business development plan, including market and risk analyses and costs.
This feasibility study will be a strong asset to advance this unique, innovative therapy towards its commercialization not only in GBM, but eventually in multiple cancer markets.
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Duración del proyecto: 5 meses
Fecha Inicio: 2016-02-16
Fecha Fin: 2016-07-31
Fecha Fin: 2016-07-31
Línea de financiación: concedida
El organismo H2020 notifico la concesión del proyecto el día 2016-07-31
Línea de financiación objetivo
El proyecto se financió a través de la siguiente ayuda:
Presupuesto
El presupuesto total del proyecto asciende a
71K€
Líder del proyecto
PEPTOMYC
La realizacion y desarrollo de estudios y proyectos de investigacion cientifica y tecnica en el ambito de las enfermedades oncologicas y tum...
Perfil tecnológico
TRL
4-5
6M
Perfil tecnológico
TRL
4-5
6M