Literature DB >> 26666772

Incentives for Starting Small Companies Focused on Rare and Neglected Diseases.

Sean Ekins1,2, Jill Wood3,4.   

Abstract

Starting biotech or pharmaceutical companies is traditionally thought to be based around a scientist, their technology platform or a clinical candidate spun out from another company. Between us we have taken a different approach and formed two small early stage companies after initially leveraging the perspective of a parent with a child with a life-threatening rare disease. Phoenix Nest ( http://www.phoenixnestbiotech.com/ ) was co-founded to work on treatments for Sanfilippo syndrome a devastating neurodegenerative lysosomal storage disorder. In the space of just over 3 years we have built up collaborations with leading scientists in academia and industry and been awarded multiple NIH small business grants. The second company, Collaborations Pharmaceuticals Inc. ( http://www.collaborationspharma.com/ ) was founded to address some of the other 7000 or so rare diseases as well as neglected infectious diseases. The Rare Pediatric Disease Priority Review Voucher is likely the most important incentive for companies working on rare diseases with very small populations. This may also be partially responsible for the recent acquisitions of rare disease companies with late stage candidates. Lessons learned in the process of starting our companies are that rare disease parents or patients can readily partner with a scientist and fund research through NIH grants rather than venture capital or angel investors initially. This process may be slow so patience and perseverance is key. We would encourage other pharmaceutical scientists to meet rare disease parents, patients or advocates and work with them to further the science on their diseases and create a source of future drugs.

Entities:  

Keywords:  Sanfilippo syndrome; Small companies; entrepreneurship; neglected diseases; rare diseases

Mesh:

Year:  2015        PMID: 26666772      PMCID: PMC4777685          DOI: 10.1007/s11095-015-1841-9

Source DB:  PubMed          Journal:  Pharm Res        ISSN: 0724-8741            Impact factor:   4.200


  15 in total

1.  Therapies for inborn errors of metabolism: what has the orphan drug act delivered?

Authors:  Sonali S Talele; Kui Xu; Anne R Pariser; M Miles Braun; Sheiren Farag-El-Massah; M Ian Phillips; Barry H Thompson; Timothy R Coté
Journal:  Pediatrics       Date:  2010-06-21       Impact factor: 7.124

2.  21st Century Cures Act wins in US House.

Authors: 
Journal:  Nat Biotechnol       Date:  2015-09       Impact factor: 54.908

3.  Experience With the Priority Review Voucher Program for Drug Development.

Authors:  Aaron S Kesselheim; Lara R Maggs; Ameet Sarpatwari
Journal:  JAMA       Date:  2015-10-27       Impact factor: 56.272

4.  Incentives to Repurpose Existing Drugs for Orphan Indications.

Authors:  Annette K Kwok; Fabian M Koenigbauer
Journal:  ACS Med Chem Lett       Date:  2015-07-23       Impact factor: 4.345

5.  An analysis of original research contributions toward FDA-approved drugs.

Authors:  Eric V Patridge; Peter C Gareiss; Michael S Kinch; Denton W Hoyer
Journal:  Drug Discov Today       Date:  2015-06-22       Impact factor: 7.851

6.  The discovery of medicines for rare diseases.

Authors:  David C Swinney; Shuangluo Xia
Journal:  Future Med Chem       Date:  2014-06       Impact factor: 3.808

7.  Multifaceted roles of ultra-rare and rare disease patients/parents in drug discovery.

Authors:  Jill Wood; Lori Sames; Allison Moore; Sean Ekins
Journal:  Drug Discov Today       Date:  2013-08-19       Impact factor: 7.851

Review 8.  Sanfilippo syndrome: a mini-review.

Authors:  M J Valstar; G J G Ruijter; O P van Diggelen; B J Poorthuis; F A Wijburg
Journal:  J Inherit Metab Dis       Date:  2008-04-04       Impact factor: 4.982

9.  Recommendations to enable drug development for inherited neuropathies: Charcot-Marie-Tooth and Giant Axonal Neuropathy.

Authors:  Lori Sames; Allison Moore; Renee Arnold; Sean Ekins
Journal:  F1000Res       Date:  2014-04-03

10.  Intracerebral administration of adeno-associated viral vector serotype rh.10 carrying human SGSH and SUMF1 cDNAs in children with mucopolysaccharidosis type IIIA disease: results of a phase I/II trial.

Authors:  Marc Tardieu; Michel Zérah; Béatrice Husson; Stéphanie de Bournonville; Kumaran Deiva; Catherine Adamsbaum; Fanny Vincent; Michael Hocquemiller; Christine Broissand; Valérie Furlan; Andrea Ballabio; Alessandro Fraldi; Ronald G Crystal; Thomas Baugnon; Thomas Roujeau; Jean-Michel Heard; Olivier Danos
Journal:  Hum Gene Ther       Date:  2014-05-05       Impact factor: 5.695

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  5 in total

1.  Repurposing the Dihydropyridine Calcium Channel Inhibitor Nicardipine as a Nav1.8 Inhibitor In Vivo for Pitt Hopkins Syndrome.

Authors:  Sean Ekins; Ana C Puhl; Audrey Davidow
Journal:  Pharm Res       Date:  2020-06-11       Impact factor: 4.200

2.  Enabling Anyone to Translate Clinically Relevant Ideas to Therapies.

Authors:  Sean Ekins; Natalie Diaz; Julia Chung; Paul Mathews; Aaron McMurtray
Journal:  Pharm Res       Date:  2016-09-12       Impact factor: 4.200

Review 3.  The Next Era: Deep Learning in Pharmaceutical Research.

Authors:  Sean Ekins
Journal:  Pharm Res       Date:  2016-09-06       Impact factor: 4.200

4.  OpenZika: An IBM World Community Grid Project to Accelerate Zika Virus Drug Discovery.

Authors:  Sean Ekins; Alexander L Perryman; Carolina Horta Andrade
Journal:  PLoS Negl Trop Dis       Date:  2016-10-20

5.  Open drug discovery for the Zika virus.

Authors:  Sean Ekins; Daniel Mietchen; Megan Coffee; Thomas P Stratton; Joel S Freundlich; Lucio Freitas-Junior; Eugene Muratov; Jair Siqueira-Neto; Antony J Williams; Carolina Andrade
Journal:  F1000Res       Date:  2016-02-09
  5 in total

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