Literature DB >> 21248312

"Creating hope" and other incentives for drug development for children.

Edward Connor1, Pablo Cure.   

Abstract

Enhancing drug development for pediatric disease is a priority and a public responsibility. The Creating Hope Act of 2010 is important new proposed legislation that adds drugs and biologics for treating rare diseases in children to those for neglected tropical diseases as eligible for a priority review voucher from the U.S. Food and Drug Administration. The Act enhances existing incentive programs through specific financial benefits to companies who seek a pediatric indication for a new drug to treat an orphan disease that occurs specifically in children.

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Year:  2011        PMID: 21248312     DOI: 10.1126/scitranslmed.3001707

Source DB:  PubMed          Journal:  Sci Transl Med        ISSN: 1946-6234            Impact factor:   17.956


  11 in total

1.  Declining childhood and adolescent cancer mortality.

Authors:  Malcolm A Smith; Sean F Altekruse; Peter C Adamson; Gregory H Reaman; Nita L Seibel
Journal:  Cancer       Date:  2014-05-22       Impact factor: 6.860

2.  Analysis of pediatric clinical drug trials for neuropsychiatric conditions.

Authors:  Srinivas Murthy; Kenneth D Mandl; Florence Bourgeois
Journal:  Pediatrics       Date:  2013-05-06       Impact factor: 7.124

3.  An integrated approach to identifying clinically relevant targets in pediatric gliomas.

Authors:  Troy A McEachron; Patrick Tomboc; Nhan L Tran
Journal:  CNS Oncol       Date:  2013-07

Review 4.  Generic Substitution of Orphan Drugs for the Treatment of Rare Diseases: Exploring the Potential Challenges.

Authors:  Antonello Di Paolo; Elena Arrigoni
Journal:  Drugs       Date:  2018-03       Impact factor: 9.546

5.  New regulatory paradigms for innovative drugs to treat pediatric diseases.

Authors:  Thomas J Hwang; Florence T Bourgeois
Journal:  JAMA Pediatr       Date:  2014-10       Impact factor: 16.193

Review 6.  Remaining challenges in childhood cancer and newer targeted therapeutics.

Authors:  Malcolm A Smith; Gregory H Reaman
Journal:  Pediatr Clin North Am       Date:  2014-10-18       Impact factor: 3.278

Review 7.  Improving access to novel agents for childhood leukemia.

Authors:  Weili Sun; Paul S Gaynon; Richard Sposto; Alan S Wayne
Journal:  Cancer       Date:  2015-02-11       Impact factor: 6.860

8.  Pharmacotherapy challenges of Fontan-associated plastic bronchitis: a rare pediatric disease.

Authors:  Kristina Brooks; Regine L Caruthers; Kurt R Schumacher; Kathleen A Stringer
Journal:  Pharmacotherapy       Date:  2013-05-17       Impact factor: 4.705

9.  Integrated genetic and pharmacologic interrogation of rare cancers.

Authors:  Andrew L Hong; Yuen-Yi Tseng; Glenn S Cowley; Oliver Jonas; Jaime H Cheah; Bryan D Kynnap; Mihir B Doshi; Coyin Oh; Stephanie C Meyer; Alanna J Church; Shubhroz Gill; Craig M Bielski; Paula Keskula; Alma Imamovic; Sara Howell; Gregory V Kryukov; Paul A Clemons; Aviad Tsherniak; Francisca Vazquez; Brian D Crompton; Alykhan F Shamji; Carlos Rodriguez-Galindo; Katherine A Janeway; Charles W M Roberts; Kimberly Stegmaier; Paul van Hummelen; Michael J Cima; Robert S Langer; Levi A Garraway; Stuart L Schreiber; David E Root; William C Hahn; Jesse S Boehm
Journal:  Nat Commun       Date:  2016-06-22       Impact factor: 14.919

10.  LC-UV/MS quality analytics of paediatric artemether formulations.

Authors:  Kirsten Vandercruyssen; Matthias D'Hondt; Valentijn Vergote; Herwig Jansen; Christian Burvenich; Bart De Spiegeleer
Journal:  J Pharm Anal       Date:  2013-04-25
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