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The Patient
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October 13, 2023
Determining Commonalities in the Experiences of Patients with Rare Diseases: A Qualitative Analysis of US Food and Drug Administration Patient Engagement Sessions
Catherine Mease, Lewis J Fermaglich, Karen Jackler, et al.
Nature Reviews. Drug Discovery
|
December 12, 2023
Trends in drug development for amyotrophic lateral sclerosis
Selma Kraft, Catherine Mease, Devanand Jillapalli, et al.
Orphanet Journal of Rare Diseases
|
March 22, 2024
Correction to: Analysis of the first ten years of FDA's rare pediatric disease priority review voucher program: designations, diseases, and drug development
Catherine Mease, Kathleen L Miller, Lewis J Fermaglich, et al.
Orphanet Journal of Rare Diseases
|
February 25, 2024
Analysis of the first ten years of FDA's rare pediatric disease priority review voucher program: designations, diseases, and drug development
Catherine Mease, Kathleen L Miller, Lewis J Fermaglich, et al.
Therapeutic Innovation & Regulatory Science
|
May 4, 2018
Common Filing Deficiencies in Abbreviated New Drug Applications Containing Clinical Endpoint Studies
Lewis J Fermaglich, Ru Chen, Carol Y Kim, et al.
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Search research articles
Search
Showing results (21-30 of 25) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 25 results.
The Patient
|
October 13, 2023
Determining Commonalities in the Experiences of Patients with Rare Diseases: A Qualitative Analysis of US Food and Drug Administration Patient Engagement Sessions
Catherine Mease, Lewis J Fermaglich, Karen Jackler, et al.
Nature Reviews. Drug Discovery
|
December 12, 2023
Trends in drug development for amyotrophic lateral sclerosis
Selma Kraft, Catherine Mease, Devanand Jillapalli, et al.
Orphanet Journal of Rare Diseases
|
March 22, 2024
Correction to: Analysis of the first ten years of FDA's rare pediatric disease priority review voucher program: designations, diseases, and drug development
Catherine Mease, Kathleen L Miller, Lewis J Fermaglich, et al.
Orphanet Journal of Rare Diseases
|
February 25, 2024
Analysis of the first ten years of FDA's rare pediatric disease priority review voucher program: designations, diseases, and drug development
Catherine Mease, Kathleen L Miller, Lewis J Fermaglich, et al.
Therapeutic Innovation & Regulatory Science
|
May 4, 2018
Common Filing Deficiencies in Abbreviated New Drug Applications Containing Clinical Endpoint Studies
Lewis J Fermaglich, Ru Chen, Carol Y Kim, et al.
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