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Trials
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January 20, 2021
Utilising benefit-risk assessments within clinical trials-a protocol for the BRAINS project
Nikki Totton, Steven Julious, Dyfrig Hughes, et al.
Pharmaceutical Statistics
|
January 12, 2018
Approaches to sample size calculation for clinical trials in rare diseases
Frank Miller, Sarah Zohar, Nigel Stallard, et al.
Nature Reviews. Drug Discovery
|
October 23, 2023
IRDiRC Drug Repurposing Guidebook: making better use of existing drugs to tackle rare diseases
Anneliene Hechtelt Jonker, Simon Day, Michela Gabaldo, et al.
Nature Reviews. Drug Discovery
|
April 22, 2020
Boosting delivery of rare disease therapies: the IRDiRC Orphan Drug Development Guidebook
Anneliene Hechtelt Jonker, Virginie Hivert, Michela Gabaldo, et al.
Orphanet Journal of Rare Diseases
|
March 4, 2017
Does the low prevalence affect the sample size of interventional clinical trials of rare diseases? An analysis of data from the aggregate analysis of clinicaltrials.gov
Siew Wan Hee, Adrian Willis, Catrin Tudur Smith, et al.
Orphanet Journal of Rare Diseases
|
November 8, 2018
Recommendations for the design of small population clinical trials
Simon Day, Anneliene Hechtelt Jonker, Lilian Pek Lian Lau, et al.
Health Technology Assessment (Winchester, England)
|
November 20, 2023
Appropriate design and reporting of superiority, equivalence and non-inferiority clinical trials incorporating a benefit-risk assessment: the BRAINS study including expert workshop
Nikki Totton, Steven A Julious, Elizabeth Coates, et al.
Clinical Trials (London, England)
|
December 6, 2014
The impact of registration of clinical trials units: the UK experience
Eleanor McFadden, Saeeda Bashir, Steve Canham, et al.
British Journal of Clinical Pharmacology
|
October 26, 2021
c4c: Paediatric pharmacovigilance: Methodological considerations in research and development of medicines for children - A c4c expert group white paper
Beate Aurich, Dina Apele-Freimane, Tobias Banaschewski, et al.
JAMA
|
December 21, 2017
Guidelines for the Content of Statistical Analysis Plans in Clinical Trials
Carrol Gamble, Ashma Krishan, Deborah Stocken, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 47) with videos related to
Sort By:
Page
of 5
Trials
|
January 20, 2021
Utilising benefit-risk assessments within clinical trials-a protocol for the BRAINS project
Nikki Totton, Steven Julious, Dyfrig Hughes, et al.
Pharmaceutical Statistics
|
January 12, 2018
Approaches to sample size calculation for clinical trials in rare diseases
Frank Miller, Sarah Zohar, Nigel Stallard, et al.
Nature Reviews. Drug Discovery
|
October 23, 2023
IRDiRC Drug Repurposing Guidebook: making better use of existing drugs to tackle rare diseases
Anneliene Hechtelt Jonker, Simon Day, Michela Gabaldo, et al.
Nature Reviews. Drug Discovery
|
April 22, 2020
Boosting delivery of rare disease therapies: the IRDiRC Orphan Drug Development Guidebook
Anneliene Hechtelt Jonker, Virginie Hivert, Michela Gabaldo, et al.
Orphanet Journal of Rare Diseases
|
March 4, 2017
Does the low prevalence affect the sample size of interventional clinical trials of rare diseases? An analysis of data from the aggregate analysis of clinicaltrials.gov
Siew Wan Hee, Adrian Willis, Catrin Tudur Smith, et al.
Orphanet Journal of Rare Diseases
|
November 8, 2018
Recommendations for the design of small population clinical trials
Simon Day, Anneliene Hechtelt Jonker, Lilian Pek Lian Lau, et al.
Health Technology Assessment (Winchester, England)
|
November 20, 2023
Appropriate design and reporting of superiority, equivalence and non-inferiority clinical trials incorporating a benefit-risk assessment: the BRAINS study including expert workshop
Nikki Totton, Steven A Julious, Elizabeth Coates, et al.
Clinical Trials (London, England)
|
December 6, 2014
The impact of registration of clinical trials units: the UK experience
Eleanor McFadden, Saeeda Bashir, Steve Canham, et al.
British Journal of Clinical Pharmacology
|
October 26, 2021
c4c: Paediatric pharmacovigilance: Methodological considerations in research and development of medicines for children - A c4c expert group white paper
Beate Aurich, Dina Apele-Freimane, Tobias Banaschewski, et al.
JAMA
|
December 21, 2017
Guidelines for the Content of Statistical Analysis Plans in Clinical Trials
Carrol Gamble, Ashma Krishan, Deborah Stocken, et al.
Page
of 5