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France's competitiveness in global pharmaceutical research: The situation is improving.
d'Andon, Anne; Galaup, Ariane; Fabron, Cecile; Detournay, Bruno; Borel, Thomas.
  • d'Andon A; CEMKA, 43, boulevard Maréchal Joffre, 92340 Bourg-La-Reine, France.
  • Galaup A; LEEM, 75858 Paris, France.
  • Fabron C; CEMKA, 43, boulevard Maréchal Joffre, 92340 Bourg-La-Reine, France. Electronic address: cecile.fabron@cemka.fr.
  • Detournay B; CEMKA, 43, boulevard Maréchal Joffre, 92340 Bourg-La-Reine, France.
  • Borel T; LEEM, 75858 Paris, France.
Therapie ; 76(6): 549-557, 2021.
Article in English | MEDLINE | ID: covidwho-1230795
ABSTRACT

AIMS:

The French pharmaceutical companies' association (LEEM) biennially carries out a study on the attractiveness of France in pharmaceutical clinical research. This study aims to measure France's global competitiveness for international clinical trials (CT) and assess its strengths and areas of excellence.

METHODS:

A descriptive and comparative analysis was conducted using the data from both the ClinicalTrials.gov registry for the 2015-2019 period and those reported in a national web-based database (OSCAR) involving the major pharmaceutical companies operating in France in 2018-2019. OSCAR allows to describe the administrative authorization and starting process for all drug trials conducted in France.

RESULTS:

Among 8607 worldwide drug trials initiated in 2019, 34.3% (n=2.954) were funded exclusively by pharmaceutical companies (52.1% in France). On average, France was involved in 10.5% of all global industrial CTs launched over 2018-2019, still ranking in the 4th position among European countries. Early-phase trials represented 17.3% of trials conducted by the drug companies in France, versus 25% in Germany and 29% in United Kingdom. Oncology remains an area of excellence in France with 18.7% of all worldwide CTs conducted in this therapeutic area over the study period involving at least some French centres, ranking France 2nd among European countries. The median of total deadline before the first patient inclusion of 204 days in 2018-2019 with no marked improvement as compared to 2016-2017 period. However, the delay getting initial trial authorization was slightly reduced and an overall deadline of 167 days was observed for CTs entered the pilot phase initiated recently by the European regulation.

CONCLUSION:

After ten difficult years, areas of excellence, such as oncology and rare diseases and more recently, the outstanding mobilization for the COVID-19 research, have enabled France to maintain its pharmaceutical research. Furthermore, a set of additional decisions would strengthen this position in the next years.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Pharmaceutical Research / COVID-19 Type of study: Prognostic study / Randomized controlled trials Limits: Humans Country/Region as subject: Europa Language: English Journal: Therapie Year: 2021 Document Type: Article Affiliation country: J.therap.2021.05.006

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Pharmaceutical Research / COVID-19 Type of study: Prognostic study / Randomized controlled trials Limits: Humans Country/Region as subject: Europa Language: English Journal: Therapie Year: 2021 Document Type: Article Affiliation country: J.therap.2021.05.006