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News Breaks
April 12, 2011
11:45 EDTNVDL, PFE
theflyonthewall.com: NovaDel Pharma develops spray to replace Viagra, Globes reports
NovaDel Pharma (NVDL) is developing a spray as an alternative to Pfizer's (PFE) Viagra pill, reports Globes. The company has already obtained FDA approval for two kinds of spray that replaces tablets for sleep disorders and angina, and will now look for FDA approval to replace Viagra when its patents expire next year. Reference Link :theflyonthewall.com



News For NVDL;PFE From The Last 14 Days
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May 25, 2012
11:13 EDTPFE
theflyonthewall.com: Chairman: Elan may get offer if Alzheimer drug data positive, Reuters says
Elan's (ELN) chairman Bob Ingram said yesterday it was possible that the company could receive a takeover offer if data on an bapineuzumab, an experimental Alzheimer's drug it has a 25% economic interest in, is positive, reported Reuters. "If an offer comes in we can't ignore it, but it is not our strategy to sell the company," Ingram says. The drug is being developed by Pfizer (PFE) and Johnson and Johnson (JNJ), Reuters noted. Reference Link :theflyonthewall.com
11:09 EDTPFE
theflyonthewall.com: Senate passes FDA funding bill, Reuters reports

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09:14 EDTPFE
theflyonthewall.com: Pfizer's Axitinib receives positive opinion from CHMP
Pfizer announced that the Committee for Human Medicinal Products of the European Medicines Agency has adopted a positive opinion regarding the marketing authorization of axitinib in the European Union for the treatment of adult patients with advanced renal cell carcinoma, a type of advanced kidney cancer, after failure of prior treatment with sunitinib or a cytokine. The CHMP's positive opinion will be reviewed by the European Commission, which has the authority to approve medicines for the EU. Pfizer anticipates a decision from the Commission in the coming months. :theflyonthewall.com

May 24, 2012
18:10 EDTPFE
theflyonthewall.com: FDA committee finds Pfizer's clinical data supports effectiveness of novel drug

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07:38 EDTPFE
theflyonthewall.com: FDA Peripheral & Central Nervous System Drugs Committee holds a meeting

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07:13 EDTPFE
theflyonthewall.com: J&J's Xarelto likely delayed 3-12 months, not dead, says Leerink
Leerink believes the FDA panel vote against approval of Johnson & Johnson's (JNJ) and Bayer's (BAYRY) Xarelto for the prevention of CV events in patients with a recent acute coronary syndrome will likely delay approval by 3-12 months, not kill the drug for this indication. The firm believes Bristol-Myers' (BMY) and Pfizer's (PFE) Eliquis could benefit slightly from a Xarelto delay. :theflyonthewall.com

May 23, 2012
07:51 EDTPFE
theflyonthewall.com: PPD, Inc. names David Simmons as chairman and CEO

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07:10 EDTPFE
theflyonthewall.com: FTC, Senate probing blocking of generic drug companies, Washington Post says
The Federal Trade Commission and the U.S. Senate are investigating whether pharmaceutical companies are using a loophole to prevent generic drug makers from obtaining samples of brand name drugs, according to The Washington Post. The FDA requires generic drug makers to test a sample of brand name versions in order to get a generic drug approved, the newspaper notes. Reference Link :theflyonthewall.com

May 21, 2012
07:38 EDTPFE
theflyonthewall.com: Sachs Associates to host a forum

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May 18, 2012
14:04 EDTPFE
theflyonthewall.com: Pfizer recalls Advil medicine, WSJ reports
Pfizer (PFE) recently recalled more than 650,000 bottles of its Advil pain relief medicine because the pills could emit a strong odor, according to The Wall Street Journal. Reference Link :theflyonthewall.com
08:04 EDTPFE
theflyonthewall.com: Pfizer announces results of studies on Lyrica capsules CV

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May 17, 2012
17:45 EDTPFE
theflyonthewall.com: FDA statement regarding azithromycin and the risk of cardiovascular death

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06:02 EDTPFE
theflyonthewall.com: Zithromax linked with deadly, but rare, heart risk, AP reports

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May 15, 2012
17:10 EDTPFE
theflyonthewall.com: Pfizer reports positive results for Phase 3 Intorsect study evaluating Torisel
Pfizer announced that the Phase 3 INTORSECT study, evaluating TORISEL in patients with advanced renal cell carcinoma whose disease had progressed on or after SUTENT therapy, did not meet the primary endpoint of prolonging progression free survival when compared to sorafenib. Although PFS was numerically higher in patients treated with temsirolimus, the difference was not statistically significant. Overall survival, a secondary endpoint in the study, showed statistical significance favoring patients randomized to the sorafenib arm. Adverse events in this study were consistent with the known safety profiles for both drugs. Full efficacy and safety data from this study will be presented at an upcoming major medical congress. :theflyonthewall.com
10:09 EDTPFE
theflyonthewall.com: Amylin climbs after report says seven companies involved in sales process

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09:37 EDTPFE
theflyonthewall.com: Summer Street's biotech research team hosts a luncheon meeting

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07:24 EDTPFE
theflyonthewall.com: Amylin draws interest from Pfizer, AstraZeneca, Sanofi, Bloomberg reports

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06:10 EDTPFE
theflyonthewall.com: On the Fly: Periodicals Wrap-Up

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May 14, 2012
08:05 EDTPFE
theflyonthewall.com: Pfizer to present new data In advanced kidney, lung and hematologic cancers

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