Innovations in Clinical Development in Rare Diseases of Children and Adults: Small Populations and/or Small Patients

Author:

Beckman Robert A.ORCID,Antonijevic Zoran,Ghadessi Mercedeh,Xu Heng,Chen Cong,Liu Yi,Tang Rui

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Pediatrics, Perinatology and Child Health

Reference58 articles.

1. Orphan Drug Act of 1983, Public Law 97-414, Stat. 2049 (1983) amended by public law 98-551 (1984) to add a numeric prevalence threshold.

2. Utilizing innovative statistical methods and trial designs in rare diseases. In: health policy. https://healthpolicy.duke.edu/sites/default/files/2020-03/backgrounder_10_11_16.pdf. Accessed 23 Dec 2021.

3. Information packet, rare diseases day 2022. In: Rare disease day. https://download2.rarediseaseday.org/2022/campaign_materials/infopack_2022.pdf Accessed 23 Dec 2021.

4. Beckman RA, Clark JC, Chen C. Integrating predictive biomarkers and classifiers into oncology drug development programs. Nat Rev Drug Discovery. 2011;10:735–49.

5. Schwartz, J. Research in rare disease: the nature and extent of evidence needed for decision. In: 51st annual meeting of the Drug information Association, session #318 (track 17), 2015, Washington, DC.

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