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The Motley Fool
November 19, 2010
Brian Orelli
Up 95%, but Still Risky as Heck That's an understatement for MELA Sciences. mark for My Articles similar articles
The Motley Fool
March 19, 2007
Brian Lawler
Is Dendreon Doomed? A pivotal FDA regulatory meeting approaches for the development-stage pharma. Investors, take note. mark for My Articles similar articles
The Motley Fool
November 29, 2007
Brian Lawler
Another Chapter in Glaxo's Relenza Saga An FDA advisory panel suggested that the Relenza label should be strengthened to include the possibility of abnormal behavior and hallucinations in those who take it. mark for My Articles similar articles
The Motley Fool
August 1, 2007
Brian Lawler
Elan Gets a Vote of Confidence Elan receives some good news from an FDA advisory panel in the form of a recommendation to expand the use of Tysabri to treat Crohn's disease. mark for My Articles similar articles
The Motley Fool
March 8, 2010
Brian Orelli
Really? A 59% Share Price Jump for That? Justified or not, InterMune skyrockets ahead of an FDA panel meeting. mark for My Articles similar articles
The Motley Fool
June 20, 2011
Brian Orelli
See Drug, Approve Drug An approval of Regeneron's macular degeneration Eylea looks likely. mark for My Articles similar articles
The Motley Fool
March 17, 2008
Brian Lawler
The Panelling on Amgen's Walls One FDA panel ruling is a win, another is much less upsetting than investors feared. mark for My Articles similar articles
The Motley Fool
June 16, 2011
Brian Orelli
No Poke in the Eye Here What's the biggest sign that the Food and Drug Administration is all set to approve Regeneron Pharmaceuticals' Eylea? The briefing documents for the advisory committee contained a proposed version of the label. mark for My Articles similar articles
The Motley Fool
December 14, 2007
Brian Lawler
Ignore the Dendreon Hoopla A Congressional probe request will have no effect on Dendreon or Provenge's odds at making it through the FDA, since it was not the FDA reviewers of the Provenge marketing application that were accused of anything bad. mark for My Articles similar articles
The Motley Fool
June 29, 2010
Brian Orelli
The Final Obstacle to Your Drug Company Multibagger The dreaded FDA advisory committee meeting. mark for My Articles similar articles
The Motley Fool
January 4, 2012
Brian Orelli
Mark Your Calendars, Biotech Investors Cell Therapeutics' advisory panel meet ought to be entertaining. mark for My Articles similar articles
The Motley Fool
August 18, 2011
Brian Orelli
Running the Correct Trial Isn't Enough MELA Sciences' stock is up on claim that their trial meets FDA guidance, but they still need to prove that the device actually works. mark for My Articles similar articles
The Motley Fool
November 17, 2010
Brian Orelli
52 Years Down, 1 Month to Go Lupus treatment Benlysta moves closer to approval. mark for My Articles similar articles
The Motley Fool
August 21, 2008
Brian Orelli
Johnson & Johnson Gets Rejected The FDA rejects Johnson & Johnson's bid to expand the label of its antibiotic. 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
The Motley Fool
September 10, 2008
Brian Lawler
A Pfizer Drug With a Cloudy Future The company offers another drug with mixed odds to the FDA. 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
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
July 28, 2010
Brian Orelli
Amplifying the Risk-Reward Ratio Amplify, Medtronic's latest, gets a mixed reaction at FDA advisory panel meeting. mark for My Articles similar articles
The Motley Fool
July 29, 2010
Brian Orelli
This FDA Panel Isn't Brilliant Why does AstraZeneca's blood thinner Brilinta work better outside the U.S. than here at home? The Food and Drug Administration's advisory panel didn't seem to have a good explanation, but they didn't appear to care much, either. mark for My Articles similar articles
The Motley Fool
April 26, 2007
Mike Havrilla
Dendreon Is Worth a Shot Provenge might be approved, which means investors might be rewarded. However, the massive short interest also highlights the tremendous risk in Dendreon. mark for My Articles similar articles
The Motley Fool
March 10, 2010
Brian Orelli
Up 160% With Room to Run You've got to love biotech and InterMune. mark for My Articles similar articles
The Motley Fool
December 5, 2011
Brian Orelli
Up 20%, but Uncertainty Still Looms Affymax is still a risky bet. mark for My Articles similar articles
The Motley Fool
July 23, 2007
Brian Lawler
GPC's Date With the FDA A document released by the FDA outlines its concerns with GPC's lead drug. Investors, take note. mark for My Articles similar articles
The Motley Fool
December 31, 2007
Brian Lawler
Lower Expectations for Theravance The FDA decides to debate Theravance's lead drug, Telavancin, leading to a drop in share price. mark for My Articles similar articles
The Motley Fool
May 29, 2009
Brian Orelli
Delayed, Reason Unknown As long as Bayer and Johnson & Johnson can answer the FDA's questions relatively quickly, it shouldn't affect the companies too much. mark for My Articles similar articles
The Motley Fool
October 19, 2010
Brian Orelli
When the Status Quo Is a Big Win The lack of an FDA rejection will do just fine. Amgen and Johnson & Johnson seemed to get through the FDA advisory panel process without much problem yesterday. mark for My Articles similar articles
The Motley Fool
November 12, 2010
Brian Orelli
Benlysta: Not Perfect, but Good Enough Human Genome should get past the FDA advisory panel next week. mark for My Articles similar articles
The Motley Fool
October 19, 2010
Brian Orelli
Why the FDA Won't Approve Lorcaserin and Qnexa (Yet) Obesity drugs get their day in front of the agency. mark for My Articles similar articles
The Motley Fool
September 9, 2011
Brian Orelli
Firing Squad, It Was Not J&J and Bayer get through their advisory panel with minimal problems. mark for My Articles similar articles
The Motley Fool
December 10, 2007
Brian Lawler
Will the FDA Clear Cardiome? The agency prepares to debate Cardiome's lead drug candidate, Vernakalant, a treatment for abnormal heart rhythms. Investors, take note. mark for My Articles similar articles
The Motley Fool
May 7, 2008
Brian Lawler
Cephalon's Long Shot Falls Short An FDA advisory panel brings bad news for the company. mark for My Articles similar articles
The Motley Fool
July 31, 2007
Brian Lawler
Avandia Can Stay An FDA advisory panel votes to allow GlaxoSmithKline's top diabetes compound, Avandia, to remain on the market. mark for My Articles similar articles
The Motley Fool
September 17, 2010
Brian Orelli
Thanks for Nothing, Fen-Phen Arena gets knocked down despite a relatively clean side-effect profile. mark for My Articles similar articles
The Motley Fool
December 3, 2010
Brian Orelli
Obesity Drug Companies Are (Still) Risky Orexigen heads before an FDA panel. mark for My Articles similar articles
The Motley Fool
February 28, 2008
Brian Lawler
FDA's Mixed Signals for Theravance The FDA gives Theravance frustrating double messages about a lead drug. mark for My Articles similar articles
The Motley Fool
February 4, 2009
Brian Orelli
Not If, but When, for Lilly At least Lilly now knows that it's just a matter of time until the anti-clotting agent wins FDA approval. mark for My Articles similar articles
The Motley Fool
December 3, 2010
Travis Hoium
Orexigen Therapeutics Shares Plunged: What You Need to Know Shares of biopharmaceutical company Orexigen Therapeutics fell 10% today after a Food and Drug Administration announcement. mark for My Articles similar articles
The Motley Fool
December 8, 2010
Brian Orelli
Up 100% With Room to Fly Orexigen gets a positive FDA panel nod. mark for My Articles similar articles
The Motley Fool
September 14, 2010
Brian Orelli
42% Drop? Really? Tell Us Something We Didn't Know. Arena Pharmaceuticals gets knocked down for no good reason. mark for My Articles similar articles
The Motley Fool
April 11, 2008
Brian Lawler
Amgen's Unsurprising Delay The FDA extends its review of an Amgen drug candidate. 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 9, 2010
Brian Orelli
Will These Drugs Get Past the FDA This Month? See what the FDA has on its decision calendar for the rest of September. mark for My Articles similar articles
The Motley Fool
July 12, 2011
Luke Timmerman
Seattle Genetics' New "Empowered Antibody" Looks Clean in FDA Staff Documents FDA reviews Seattle Genetics' Hodgkin's lymphoma drug. mark for My Articles similar articles
The Motley Fool
May 3, 2010
Brian Orelli
While You Were Reveling in Dendreon's Win The FDA has approved Vimovo, an arthritis drug from Pozen and AstraZeneca, and Bristol-Myers Squibb also got a decision from the FDA, but it wasn't the positive kind. 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
December 6, 2010
Brian Orelli
3-Month Delay? No Problem! Investors shrug off HGS' Benlysta delay. The Food and Drug Administration's delaying its decision on whether to approve Human Genome Sciences and GlaxoSmithKline's Benlysta shouldn't come as much of a surprise. mark for My Articles similar articles
The Motley Fool
August 31, 2009
Brian Orelli
Good Luck, Genzyme -- You'll Need It The drugmaker faces an FDA advisory-panel showdown regarding its leukemia drug Clolar. mark for My Articles similar articles
The Motley Fool
December 6, 2007
Brian Lawler
Genentech Voted Down An FDA panel recommends against expanded use of Genentech's lead drug. mark for My Articles similar articles
The Motley Fool
December 10, 2008
Brian Orelli
A Painless Advisory Panel Meeting Genzyme might be getting a Christmas present from the Food and Drug Administration. An FDA advisory panel unanimously recommended approval for Genzyme's osteoarthritis pain drug Synvisc-One. mark for My Articles similar articles