PMC:7784828 / 11491-13074 JSONTXT 2 Projects

Annnotations TAB TSV DIC JSON TextAE

Id Subject Object Predicate Lexical cue
T105 0-144 Sentence denotes The process of drug research and development is extremely slow taking at least 7 to 10 years for a lead candidate to reach the marketplace [28].
T106 145-300 Sentence denotes This is mainly due to the rigorous process needed to ensure safety and efficacy through clinical human trial and as well as obtaining regulatory approvals.
T107 301-408 Sentence denotes Duplication and reproducibility are other factors that also contributes to the slow pace of drug discovery.
T108 409-634 Sentence denotes While duplication and reproducibility can be seen as a squander of time and resources, they remain essential to provide more data and evidence and ensure the safety and efficiency before they are prescribed to the population.
T109 635-881 Sentence denotes The devastating malformations of children born to women prescribed ‘Thalidomide’, to treat morning sickness is a stark reminder of the important of independent rigorous evaluation of a drug’s safety profile before its release for population [31].
T110 882-1073 Sentence denotes A more recent example, hydroxychloroquine as a treatment for COVID-19, highlights the importance of multiple and independent studies needed to demonstrate a drug’s safety and efficiency [32].
T111 1074-1275 Sentence denotes Other factors include, suboptimal collaboration or lack of meaningful collaborative efforts among academia, industry, and government institutions despite several effort to encourage collaboration [33].
T112 1276-1416 Sentence denotes This have led, on many instances, to academics and pharma sectors working on similar ideas in parallel, in secret, and often in competition.
T113 1417-1583 Sentence denotes Therefore, the establishment of a trusted and fair framework of collaboration and data sharing can both speed up the pace and improve the outcome of successful drugs.