Sign up for a free trial now
  • Login
  • Subscribe
  • Take a FREE Trial
  • About Us
  • Contact us
  • RSS

24 May 2013


The Pharma Letter
  • Home
  • 7 Day Premium Trial
  • Pharmaceuticals
  • Biotechnology
  • Generics
  • Events
  • Companies
  • Drugs
  • Subscribe

Nuvigil Articles

Teva settles Nuvigil patent litigation with Mylan, which debuts generic Doryx

1 May 2012

Opportunities for Pharma in narcolepsy

20 February 2012

Lundbeck to expand opportunities in Canada and Latin America with Cephalon products

10 February 2011

US marketing delay for MannKind’s Afrezza and Cephalon drops Nuvigil for jet lag

4 January 2011

US FDA calls for more data on Cephalon’s Nuvigil for jet lag sleepiness, as firm receives setback in pay-for-delay deal on Provigil

30 March 2010

Mylan confirms first-to-file patent challenge to Cephalon’s sleep-disorder drug Nuvigil

12 January 2010

FDA eyes orlistat for potential liver problems, Chantix under scrutiny for skin reaction

5 June 2009

Nuvigil shows strong Ph III data in jet lag

9 April 2009

US study suggests abuse potential for Cephalon's Provigil

23 March 2009

Cephalon's Nuvigil gets tentative OK from FDA

9 April 2007

Stock Commentary - New York week to April 2

9 April 2007

Stock Commentary - New York week to Feb 19, 2007

26 February 2007

Stock Commentary - New York week to Dec 11, 2006

18 December 2006

Cephalon updates on final Nuvigil labeling

11 December 2006

Cephalon/Takeda to promote Provigil in US

19 June 2006

Provagil "improves wakefulness"

15 August 2005

Cephalon files NDA with FDA for Nuvigil

11 April 2005

Positive Ph III data for Cephalon's Nuvigil

21 February 2005

Showing 1-18 of 18 articles

Go to beginningPrevious
  • 1
NextGo to end
  • Hot Topics
  • Most Read
  • US FDA advisory panel backs approval of Merck & Co's suvorexant, but only at lower doses
  • Alchemia and Merck Serono collaborate on HA-Irinotecan with Erbitux
  • AstraZeneca's naloxegol meets endpoints; EMA validates Gilead's sofosbuvir MAA
  • Boehringer Ingelheim gets FDA warning letter on cGMP failures
  • Italy's pharma market slump set to continue, warns GlobalData
  • US FDA advisory panel backs approval of Merck & Co's suvorexant, but only at lower doses
  • Alchemia and Merck Serono collaborate on HA-Irinotecan with Erbitux
  • AstraZeneca's naloxegol meets endpoints; EMA validates Gilead's sofosbuvir MAA
  • Boehringer Ingelheim gets FDA warning letter on cGMP failures
  • Italy's pharma market slump set to continue, warns GlobalData

30 Day Premium Trial


Events

Twitter Right banner

RSS



© 2013 thepharmaletter.com

  • Home
  • RSS
  • About Us
  • Subscribe
  • Terms and Conditions
  • Article Archive
Site powered by WORKSsitebuilder CMS