Projektdetails
Beschreibung
RealiseD implements a collaborative and compRehensive mEthodological and operational Approach to cLinical trIalS in rarE Diseases
enabling timely drug development and approval centred on patients’ needs with high level of evidence reachable in a limited
environment. The core of RealiseD operational approaches includes the systematic procedures for patients’ referral, the certification
of
clinical sites and filling the gaps for successful development of rare and ultra rare diseases[(U)RD]’ clinical trials using 4 (U)RD diseases
from 4 European Research Networks (ERNs). RealiseD methodological teams will optimise innovative statistical and quantitative
approaches for design and analysis of (U)RD-CTs developed in the past 10 years and refined in the last years to facilitate the regulatory
pathway for innovative drug development. RealiseD is implemented in a public private partnership consortium including regulators
and HTA bodies representatives to co-create operational and methodological approaches in an iterative procedure using a
multistakeholders’ agreement process. RealiseD will increase the incentives and motivation for the pharmaceutical industry by
reducing many uncertainties on the path of drug development in (U)RD that will follow widely accepted rules. To achieve these
innovative approaches, RealiseD will capitalise on an international multistakeholders effort as the problem in (U)RD drug
development cannot be solved in a restricted geographical area. With the development and deployment of playbooks arising from
the
co-created developments, RealiseD will ascertain visibility and readiness of the innovations. The overall ambition of RealiseD is to
change the paradigm of CT design for U(RD) by enlarging the spectrum of methodological and operational approaches and to
establish a sustainable, innovative, and optimised CT paradigm for U(RD) medicinal product development programs, while
maximizing the acceptance by all stakeholders.
enabling timely drug development and approval centred on patients’ needs with high level of evidence reachable in a limited
environment. The core of RealiseD operational approaches includes the systematic procedures for patients’ referral, the certification
of
clinical sites and filling the gaps for successful development of rare and ultra rare diseases[(U)RD]’ clinical trials using 4 (U)RD diseases
from 4 European Research Networks (ERNs). RealiseD methodological teams will optimise innovative statistical and quantitative
approaches for design and analysis of (U)RD-CTs developed in the past 10 years and refined in the last years to facilitate the regulatory
pathway for innovative drug development. RealiseD is implemented in a public private partnership consortium including regulators
and HTA bodies representatives to co-create operational and methodological approaches in an iterative procedure using a
multistakeholders’ agreement process. RealiseD will increase the incentives and motivation for the pharmaceutical industry by
reducing many uncertainties on the path of drug development in (U)RD that will follow widely accepted rules. To achieve these
innovative approaches, RealiseD will capitalise on an international multistakeholders effort as the problem in (U)RD drug
development cannot be solved in a restricted geographical area. With the development and deployment of playbooks arising from
the
co-created developments, RealiseD will ascertain visibility and readiness of the innovations. The overall ambition of RealiseD is to
change the paradigm of CT design for U(RD) by enlarging the spectrum of methodological and operational approaches and to
establish a sustainable, innovative, and optimised CT paradigm for U(RD) medicinal product development programs, while
maximizing the acceptance by all stakeholders.
| Akronym | RealiseD |
|---|---|
| Status | Nicht begonnen |
| Tatsächlicher Beginn/ -es Ende | 1/01/25 → 31/12/29 |