MagPortal.com   Clustify - document clustering
 Home  |  Newsletter  |  My Articles  |  My Account  |  Help 
Similar Articles
The Motley Fool
January 25, 2007
Brian Lawler
Discovery Finds Its Way Even though Discovery Laboratories has been in control of its manufacturing plant for only one of the approvable letters, another failure to get approval of Surfaxin will probably be strike three for most investors. mark for My Articles similar articles
The Motley Fool
May 28, 2008
Brian Lawler
Discovery's Costly Debt Delay Discovery Labs announces a new financing agreement, but it's an expensive arrangement. mark for My Articles similar articles
The Motley Fool
May 5, 2008
Brian Orelli
A Short Wait for Discovery Labs? The company gets a third letter about Surfaxin, but should be able to satisfy the FDA soon. mark for My Articles similar articles
The Motley Fool
April 29, 2008
Brian Orelli
Will These Drugs Get FDA Approval? Discovery Laboratories and Adolor are waiting FDA decisions on their drugs next month. mark for My Articles similar articles
The Motley Fool
February 27, 2007
Brian Lawler
FDA Keeps Novartis Waiting The pharmaceutical experiences a regulatory setback in the U.S. for one of its top drug candidates. Investors, take note. mark for My Articles similar articles
The Motley Fool
April 17, 2007
Brian Lawler
Neurochem Must Wait The FDA delays a regulatory decision on Neurochem's lead compound. Investors, take note. mark for My Articles similar articles
The Motley Fool
June 21, 2007
Brian Lawler
Pfizer Gets Held Up The FDA issues an approvable letter for its novel HIV compound. Investors, take note. mark for My Articles similar articles
The Motley Fool
May 9, 2007
Brian Lawler
Diagnosing Dendreon Postmortem The FDA issues an approvable letter for Dendreon's top compound. Investors, take note. mark for My Articles similar articles
The Motley Fool
December 3, 2007
Brian Orelli
Nebivolol's Almost Approvable Letter Forest and Mylan get an approvable letter for Nebivolol. mark for My Articles similar articles
The Motley Fool
December 22, 2003
Alyce Lomax
Losing Faith in Inspire Delay for its dry-eye treatment leaves investors uninspired. mark for My Articles similar articles
The Motley Fool
June 15, 2007
Brian Lawler
Encysive's Date With Destiny Approaches A decision on the specialty drugmaker's lead drug is imminent. Betting against the FDA is generally not a good idea for investors. Here are statements from Encysive's past press releases about Thelin mark for My Articles similar articles
The Motley Fool
December 29, 2006
Brian Lawler
Third Time's the Charm for Encysive? It seems like every other week we hear about a new delay for Encysive's lead drug Thelin. With shares of Encysive down more than 20% yesterday, investors can only hope that the third time is the charm for Thelin's approval from the FDA. mark for My Articles similar articles
The Motley Fool
June 15, 2007
Brian Lawler
Neurocrine Moves Ahead Neurocrine resubmits a marketing application for its lead drug. Investors, take note. mark for My Articles similar articles
The Motley Fool
December 27, 2010
Brian Orelli
FDA Kicks Dust on Alimera's Fairy Tale Eight months after its IPO, Alimera gets hammered. mark for My Articles similar articles
The Motley Fool
July 18, 2007
Brian Lawler
More Misery for Neurochem It's hard to find another drug developer that has mishandled its correspondence with investors about its drug candidates as badly as Neurochem has over the past year. mark for My Articles similar articles
The Motley Fool
July 25, 2006
Brian Lawler
Strike Two for Encysive The FDA still won't quite give Thelin a thumbs-up. For now, Encysive investors can only sit and wait. mark for My Articles similar articles
The Motley Fool
September 24, 2007
Brian Lawler
Encysive Hears the Voice of Reason To please the FDA, Encysive Pharmaceuticals announces it is planning an additional phase 3 trial to try and bring its lead drug, Thelin, to market in the United States. mark for My Articles similar articles
The Motley Fool
October 31, 2007
Brian Lawler
Adams On-and-Off With the FDA A new compound gets delayed, but the drugmaker still raises earnings guidance, and shares rise. Investors, take note. mark for My Articles similar articles
The Motley Fool
November 8, 2006
Brian Lawler
Stumbling Block for Adolor Another approvable letter from the FDA means investors may have to be patient. mark for My Articles similar articles
The Motley Fool
July 19, 2007
Brian Lawler
Will Encysive's FDA Challenge Fail? The pharmaceutical gets set for a showdown with the FDA. Investors should think long and hard about whether shares of Encysive are worth holding, considering that the likely result of this dispute resolution process won't be positive. mark for My Articles similar articles
The Motley Fool
August 12, 2008
Brian Lawler
The FDA Stands Up Cardiome What does the approvable letter mean for Cardiome and other drug developers? mark for My Articles similar articles
The Motley Fool
August 17, 2007
Brian Orelli
Fewer Drug Approvals? Buy! Stricter standards at the FDA could create a buying opportunity. Drug approvals are down one third this year, creating a lot of value in pharmaceutical and biotech companies. Just choose your medicines carefully. mark for My Articles similar articles
The Motley Fool
December 10, 2007
Brian Lawler
Neurochem's Sure Bet at Failure Investors should add another regulatory date to their biotech calendars, this one regarding Neurochem's lead drug, KIACTA. mark for My Articles similar articles
The Motley Fool
May 14, 2007
Brian Lawler
Dendreon Tries to Pick Up the Pieces Dendreon lays out its preliminary plans following a negative FDA regulatory decision. Investors shouldn't necessarily take the smashed-down share price as indicative of a possible biotech value play. mark for My Articles similar articles
The Motley Fool
January 17, 2007
Brian Lawler
Dendreon in the Fast Lane The FDA speeds up review of Dendreon's leading drug candidate. Investors, take note. mark for My Articles similar articles
The Motley Fool
June 12, 2007
Brian Lawler
Adolor Is Still Swinging The drugmaker bumps into the FDA as it pushes to do more testing of Entereg. mark for My Articles similar articles
The Motley Fool
June 18, 2007
Brian Lawler
The Third Time Isn't the Charm for Encysive The approvable letter for the pulmonary arterial hypertension treatment marks the third time Thelin has failed to get full approval from the FDA. Investors, take note. mark for My Articles similar articles
The Motley Fool
January 16, 2008
Brian Orelli
Headache Almost Over for Pozen The drug is safe; hopefully that's all the FDA wanted to know. mark for My Articles similar articles
The Motley Fool
October 8, 2007
Brian Orelli
Pozen Submits Safety Data Will Pozen's response to its second approvable letter be enough? Investors may want to take this with a grain of salt. mark for My Articles similar articles
BusinessWeek
June 12, 2006
Catherine Arnst
Going From The Lab To Limbo The FDA has been delaying decisions on applications, and drugmakers are fuming. mark for My Articles similar articles
The Motley Fool
January 31, 2011
Brian Orelli
5 Drugmakers Headed Back to the Drawing Board Sometimes an FDA rejection is more of a to-do list. mark for My Articles similar articles
The Motley Fool
July 10, 2008
Brian Orelli
The Death of the Approvable Letter The name's changing, but for investors, little else will. mark for My Articles similar articles
The Motley Fool
September 26, 2007
Brian Lawler
Following the Fallen Biotech Class of 2006 Let's take a look a list of the biggest development stage drugmaker disasters from 2006 and how the tiny drug developers have fared since they announced their clinical trial or regulatory failures. mark for My Articles similar articles
The Motley Fool
October 16, 2007
Brian Orelli
Pozen Hedges Its Bets As promised, Pozen and partner GlaxoSmithKline announce that the pair have submitted a response to their approvable letter for Trexima, and that they plan to do an additional just-in-case safety trial. mark for My Articles similar articles
The Motley Fool
December 15, 2006
Brian Lawler
Reformatting Encysive Yet another delay from the FDA leaves investors hanging. mark for My Articles similar articles
The Motley Fool
October 30, 2007
Billy Fisher
Is Forest Labs' Nebivolol Ready for Prime Time? Shareholders of the pharmaceutical company have been looking for a way to boost their floundering stock. The FDA's likely approval of hypertension drug Nebivolol may be the answer. mark for My Articles similar articles
The Motley Fool
November 3, 2009
Brian Orelli
A Little Distracted, Are You, Merck? The FDA rejects its latest application. mark for My Articles similar articles
The Motley Fool
May 30, 2008
Brian Orelli
No Love for Antibiotics From the FDA Wyeth gets an approvable letter for its antibiotic Tygacil. mark for My Articles similar articles
The Motley Fool
April 3, 2007
Brian Lawler
Dendreon's Positive Panel Surprise Shares of the drugmaker jump after a FDA advisory panel finds in favor of its lead cancer compound. mark for My Articles similar articles
The Motley Fool
August 8, 2007
Brian Lawler
Dendreon Plods Along The turbulent drug developer releases its second-quarter financial results. Investors, take note. mark for My Articles similar articles
The Motley Fool
September 6, 2007
Brian Lawler
Encysive, Please Stop Its failure to acquiesce to the FDA's request means the competition is going forward as this drugmaker's product stays stagnant. Investors, take note. mark for My Articles similar articles
The Motley Fool
November 8, 2007
Charly Travers
BioMarin Tips Its Hand BioMarin Pharmaceutical awaits an FDA decision on its drug Kuvan for the treatment of phenylketonuria. The company's recent conference call implies approval is imminent. mark for My Articles similar articles
The Motley Fool
August 3, 2007
Brian Orelli
Another Headache for Pozen Investors Drugmaker Pozen might have to run one more trial for the FDA for its migraine drug. mark for My Articles similar articles
The Motley Fool
January 14, 2008
Brian Lawler
Score One for Dendreon and Disclosure A prestigious journal supports Dendreon's potential prostate cancer treatment, and makes a compelling case for more FDA disclosure. mark for My Articles similar articles
The Motley Fool
November 15, 2006
Alyce Lomax
A Very Complicated Discovery Complexity rules in Discovery Holding's third-quarter results. Investors, take note. mark for My Articles similar articles
Information Today
February 26, 2015
NISO Releases White Paper on the Future of Library Resource Discovery NISO (National Information Standards Organization) published a white paper, "The Future of Library Resource Discovery," which summarizes the current discovery environment. mark for My Articles similar articles
The Motley Fool
October 9, 2006
Brian Lawler
New Drug for New River An approvable letter from the FDA sends shares of New River Pharmaceuticals up. mark for My Articles similar articles
The Motley Fool
January 14, 2005
W.D. Crotty
An FDA OK That Hurts EPIX Pharmaceuticals gets a qualified "yes" from the FDA, sending its stock tumbling. mark for My Articles similar articles
IndustryWeek
October 19, 2011
FDA: A Future Innovation Partner? Could the Food and Drug Administration reform itself to help manufacturers create new medical technologies? mark for My Articles similar articles
The Motley Fool
December 31, 2010
Brian Orelli
2010 FDA Approvals and a Look Ahead Recent history can help us handicap FDA decisions. mark for My Articles similar articles