2022
Identifying obstacles hindering the conduct of academic-sponsored trials for drug repurposing on rare-diseases: an analysis of six use cases
DEL ÁLAMO, Marta, Christoph BÜHRER, Dirk FISHER, Matthias GRIESE, Paul LINGOR et. al.Základní údaje
Originální název
Identifying obstacles hindering the conduct of academic-sponsored trials for drug repurposing on rare-diseases: an analysis of six use cases
Autoři
DEL ÁLAMO, Marta (724 Španělsko, garant), Christoph BÜHRER, Dirk FISHER, Matthias GRIESE, Paul LINGOR, Giovanni PALLADINI, Nicolas SIREAU, Virginie HIVERT, Luca SANGIORGI, Florence GUILLOT, Juliane HALFTERMEYER, Lenka SOUČKOVÁ (203 Česká republika, domácí), Kristýna NOSKOVÁ (203 Česká republika, domácí) a Regina DEMLOVÁ (203 Česká republika, domácí)
Vydání
TRIALS, ENGLAND, LONDON, 2022, 1745-6215
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30104 Pharmacology and pharmacy
Stát vydavatele
Velká Británie a Severní Irsko
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 2.500
Kód RIV
RIV/00216224:14110/22:00126687
Organizační jednotka
Lékařská fakulta
UT WoS
000854766200006
Klíčová slova anglicky
Randomized clinical trials; Rare diseases; Drug repurposing; Academic-sponsored; Barriers; Challenges
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 30. 11. 2022 14:06, Mgr. Tereza Miškechová
Anotace
V originále
Background Academic-sponsored trials for rare diseases face many challenges; the present paper identifies hurdles in the set-up of six multinational clinical trials for drug repurposing, as use cases. Methods Six academic-sponsored multinational trials aiming to generate knowledge on rare diseases drug repurposing were used as examples to identify problems in their set-up. Coordinating investigators leading these trials provided feedback on hurdles linked to study, country, and site set up, on the basis of pre-identified categories established through the analysis of previous peer-reviewed publications. Results Administrative burden and lack of harmonization for trial-site agreements were deemed as a major hurdle. Other main identified obstacles included the following: (1) complexity and restriction on the use of public funding, especially in a multinational set up, (2) drug supply, including procurement tendering rules and country-specific requirements for drug stability, and (3) lack of harmonization on regulatory requirements to get trial approvals. Conclusion A better knowledge of the non-commercial clinical research landscape and its challenges and requirements is needed to make drugs-especially those with less commercial gain-accessible to rare diseases patients. Better information about existing resources like research infrastructures, clinical research programs, and counseling mechanisms is needed to support and guide clinicians through the many challenges associated to the set-up of academic-sponsored multinational trials.
Návaznosti
LM2018128, projekt VaV |
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825575, interní kód MU |
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