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Pfizer Inc. Message Board

megapickm 36 posts  |  Last Activity: Nov 18, 2013 1:05 PM Member since: Aug 16, 2013
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  • This is your opportunity to minimum double or triple your money on upcoming Mega Phase 3 Results which coming any day now (4Q13) .
    This undiscovered Stock trading at $2.09 which is very close to all time low but what you should know is that Pharma Giant Glaxo (GSK) bought their 10 Million shares over $6++ and Management bought over $5++ and they never sold NONE OF THIS .

    Migalastat for the treatment of Fabry disease a rare disease is in Phase 3 which is Partnered with GSK . If the Phase 3 is positive then it has Blockbuster Potential and the Low Float Stock will run like ACAD or RMTI .

    Top‐Line 12‐Month Data from Phase 3 Fabry Monotherapy Study 011 in 4Q

    My Target is $15-20 quickly after Positive Phase 3 data .GLTA

    Amicus Therapeutics (FOLD)

    Market Cap : $103 M
    Cash $61 M
    Price : $2.09

    Shares Out 49.6 M ( Institutions & Managament holding 46 M Shares)

    Glaxo hiked its stake in Amicus to 19.9%. Glaxo made an investment of $18.6 million and bought 2,949,581 shares of Amicus at $6.30 per share. We note that as of March 31, 2012, Glaxo's holding in Amicus was 14.8%, representing an equity investment of $31 million. We believe that Glaxo's increased holding in Amicus reflects its confidence in Amicus' pipeline.

    Fabry is a rare inherited disease that affects between 5,000 and 10,000 people worldwide. It’s caused by the deficiency of a specific enzyme that breaks down a fat known as globotriaosylceramide (GL-3). Without the enzyme, GL-3 builds up in blood vessels, causing a host of side effects including severe kidney damage.

    Fabry is currently treated with enzyme-replacement therapies, such as agalsidase (Fabrazyme), which are administered intravenously. Amicus’ drug is a pill. Agalsidase, sold by Sanofi/Genzyme, is the only drug approved to treat Fabry in the U.S.

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  • Check it out guys you have the MEGA opportunity to buy this significantly underpriced stock at the bottom if you want to make money !

    AEZS has already a Drug on the Market which is partnered with pharma giant Merck (MRK) , this Product brings around $70 M in annual revenue to AEZS thats almost two times higher than current Market Cap .

    AEZS has another Drug awaiting FDA approval and muliple Cancer Drugs in Late Stage some of them have potential Blockbusters .

    I think AEZS has the potential for a runup to minimum to $4-5 before FDA decision in Mid 2014 . GL

    AEterna Zentaris (AEZS)

    Market Cap: $43 M
    Cash: $25 M
    Price: $1.35

    Shares Out: 32 M

    Annual Revenue :$ 70 M

    BIG PIPELINE :

    Macimorelin Acetate (AEZS-130)

    Diagnostic in adult growth hormonedeficiency (endocrinology) Awaiting FDA approval

    Product ..Zoptarelin Doxorubicin (AEZS-108)

    Endometrial cancer in Phase 3

    Tripl-negative breast cancer In Phase 2

    Castration-and taxane-resistant prostate cancer in Phase 2

    Refractory bladder cancer in Phase 2

    Ovarian cancer (completed) in Phase 2

    Product ..Ozarelix :

    Prostate cancer in Phase 2

    Product ..Macimorelin Acetate (AEZS-130)

    Therapeutic in cancer cachexia in Phase 2

    Product ..Perifosine

    Multiple cancers in Phase 2
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  • Check it out guys and buy this significantly underpriced stock atthe bottom if you want to make money .GLTA

    This one is definitely one of the cheapest FDA Plays out there .

    Ticker: AEZS

    Market Cap: $42 M
    Cash: $25 M

    Shares Out: 32 M

    Aeterna Zentaris Inc. (AEZS) today announced that it has submitted a New Drug Application ("NDA") to the U.S. Food and Drug Administration ("FDA") for its ghrelin agonist, macimorelin acetate (AEZS-130). Phase 3 data have demonstrated that the compound has the potential to become the first orally-approved product that induces growth hormone release to evaluate adult growth hormone deficiency ("AGHD"), with accuracy comparable to available intravenous and intramuscular testing procedures.

    David Dodd, President and CEO of Aeterna Zentaris, commented, "The submission of the NDA to the FDA is another major milestone in our strategy to bring macimorelin acetate to market as the first approved oral product for AGHD evaluation. We are also looking at potential expansion into traumatic brain injury victims and pediatrics which would represent significant growth opportunities for the Company. Finally, I would like to congratulate and thank all those involved in our drug development and regulatory affairs departments for this exciting accomplishment."
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  • Unknown Gem with Brutal Upside Potential ...GLTA

    2 Big Drugs awaiting FDA approval another 1 NDA filing for "Best in Class" Potency Drug and 1 ANDA filing for CHF will follow within 6 months .

    NDA submission for our anti-migraine VersaFilm(TM) product had been accepted for review, with an FDA-assigned PDUFA date of February 3, 2014.
    (According to Merck's most recent annual report, sales of Maxalt(R) were $638 million in 2012.)

    IntelGenx Announces Submission of ANDA for Buprenorphine/Naloxone Sublingual Film Product for the Treatment of Opiate Addiction
    (According to IMS Health, U.S. retail sales of Suboxone(R) Sublingual Film were approximately $1.5 billion in 2012.)

    Only 20 M on the float ..IGXT has the Potential to hit $8++ within 2 Year ! GLTA

    Intelgenx (IGXT)

    Market Cap : $27 M
    Cash: $3 M
    Price:0.52

    Burn-Rate : $2 M a year
    Shares Out : 51 M ( 30 M shares are held by Investors )

    IGXT´s Monster Pipeline :

    Product ......Application......... Status of Development

    INT0004/2006 Antidepressant -- US launch in 4Q 2012

    INT0008/2007 Migraine -- PDUFA Date on Feb 3 2014

    INT0007/2006 Erectile Dysfunction -- NDA filing lin early 2014

    INT0001/2004 CHF (Coronary Heart Failure), Hypertension -- ANDA filing in early 2014

    INT0027/2011 Undisclosed Partnered with Par Pharma -- ANDA under review by FDA

    INT0020/2010 Insomnia -- in Pivotal Study

    INT0024/2010 Idiopathic pulmonary fibrosis -- in Pivotal Study

    INT0028/2011 Cancer pain (cannabinoid) --in Pivotal Study

    INT0030/2011 Animal health -- in Pivotal Study

    INT0031/2012 Benign prostatic hyperplasia --in Pivotal Study
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  • Reply to

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    by megapickm Nov 6, 2013 8:30 AM
    megapickm megapickm Nov 6, 2013 8:31 AM Flag

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    megapickm megapickm Nov 6, 2013 8:30 AM Flag

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    by megapickm Nov 6, 2013 8:30 AM
    megapickm megapickm Nov 6, 2013 8:30 AM Flag

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    by megapickm Nov 6, 2013 8:30 AM
    megapickm megapickm Nov 6, 2013 8:30 AM Flag

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    by megapickm Nov 6, 2013 8:30 AM
    megapickm megapickm Nov 6, 2013 8:30 AM Flag

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    by megapickm Nov 6, 2013 8:30 AM
    megapickm megapickm Nov 6, 2013 8:30 AM Flag

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  • megapickm by megapickm Nov 6, 2013 8:30 AM Flag

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  • Unknown Gem with Brutal Upside Potential ...GLTA

    2 Big Drugs awaiting FDA approval another 1 NDA filing for "Best in Class" Potency Drug and 1 ANDA filing for CHF will follow within 6 months .

    NDA submission for our anti-migraine VersaFilm(TM) product had been accepted for review, with an FDA-assigned PDUFA date of February 3, 2014.
    (According to Merck's most recent annual report, sales of Maxalt(R) were $638 million in 2012.)

    IntelGenx Announces Submission of ANDA for Buprenorphine/Naloxone Sublingual Film Product for the Treatment of Opiate Addiction
    (According to IMS Health, U.S. retail sales of Suboxone(R) Sublingual Film were approximately $1.5 billion in 2012.)

    Only 20 M on the float ..IGXT has the Potential to hit $8++ within 2 Year ! GLTA

    Intelgenx (IGXT)

    Market Cap : $27 M
    Cash: $3 M
    Price:0.52

    Burn-Rate : $2 M a year
    Shares Out : 51 M ( 30 M shares are held by Investors )

    IGXT´s Monster Pipeline :

    Product ......Application......... Status of Development

    INT0004/2006 Antidepressant -- US launch in 4Q 2012

    INT0008/2007 Migraine -- PDUFA Date on Feb 3 2014

    INT0007/2006 Erectile Dysfunction -- NDA filing lin early 2014

    INT0001/2004 CHF (Coronary Heart Failure), Hypertension -- ANDA filing in early 2014

    INT0027/2011 Undisclosed Partnered with Par Pharma -- ANDA under review by FDA

    INT0020/2010 Insomnia -- in Pivotal Study

    INT0024/2010 Idiopathic pulmonary fibrosis -- in Pivotal Study

    INT0028/2011 Cancer pain (cannabinoid) --in Pivotal Study

    INT0030/2011 Animal health -- in Pivotal Study

    INT0031/2012 Benign prostatic hyperplasia --in Pivotal Study
    -

  • Unknown Gem with Brutal Upside Potential ...GLTA

    2 Big Drugs already under review by FDA another 1 NDA filing for "Best in Class" Potency Drug and 1 ANDA filing for CHF will follow within 6 months .

    NDA submission for our anti-migraine VersaFilm(TM) product had been accepted for review, with an FDA-assigned PDUFA date of February 3, 2014.
    (According to Merck's most recent annual report, sales of Maxalt(R) were $638 million in 2012.)

    IntelGenx Announces Submission of ANDA for Buprenorphine/Naloxone Sublingual Film Product for the Treatment of Opiate Addiction
    (According to IMS Health, U.S. retail sales of Suboxone(R) Sublingual Film were approximately $1.5 billion in 2012.)

    Only 20 M on the float ..IGXT has the Potential to hit $10++ within 2 Year ! GLTA

    Intelgenx (IGXT)

    Market Cap : $27 M
    Cash: $3 M
    Price:0.52

    Burn-Rate : $2 M a year
    Shares Out : 51 M ( 30 M shares are held by Investors )

    IGXT´s Monster Pipeline :

    Product ......Application......... Status of Development

    INT0004/2006 Antidepressant -- US launch in 4Q 2012

    INT0008/2007 Migraine -- PDUFA Date on Feb 3 2014

    INT0007/2006 Erectile Dysfunction -- NDA filing lin early 2014

    INT0001/2004 CHF (Coronary Heart Failure), Hypertension -- ANDA filing in early 2014

    INT0027/2011 Undisclosed Partnered with Par Pharma -- ANDA under review by FDA

    INT0020/2010 Insomnia -- in Pivotal Study

    INT0024/2010 Idiopathic pulmonary fibrosis -- in Pivotal Study

    INT0028/2011 Cancer pain (cannabinoid) --in Pivotal Study

    INT0030/2011 Animal health -- in Pivotal Study

    INT0031/2012 Benign prostatic hyperplasia --in Pivotal Study
    -

  • Unknown Gem with Brutal Upside Potential ...GLTA

    2 Big Drugs already under review by FDA another 1 NDA filing for "Best in Class" Potency Drug and 1 ANDA filing for CHF will follow within 6 months .

    NDA submission for our anti-migraine VersaFilm(TM) product had been accepted for review, with an FDA-assigned PDUFA date of February 3, 2014.
    (According to Merck's most recent annual report, sales of Maxalt(R) were $638 million in 2012.)

    IntelGenx Announces Submission of ANDA for Buprenorphine/Naloxone Sublingual Film Product for the Treatment of Opiate Addiction
    (According to IMS Health, U.S. retail sales of Suboxone(R) Sublingual Film were approximately $1.5 billion in 2012.)

    Only 20 M on the float ..IGXT has the Potential to hit $10++ within 2 Year ! GLTA

    Intelgenx (IGXT)

    Market Cap : $27 M
    Cash: $3 M
    Price:0.52

    Burn-Rate : $2 M a year
    Shares Out : 51 M ( 30 M shares are held by Investors )

    IGXT´s Monster Pipeline :

    Product ......Application......... Status of Development

    INT0004/2006 Antidepressant -- US launch in 4Q 2012

    INT0008/2007 Migraine -- PDUFA Date on Feb 3 2014

    INT0007/2006 Erectile Dysfunction -- NDA filing lin early 2014

    INT0001/2004 CHF (Coronary Heart Failure), Hypertension -- ANDA filing in early 2014

    INT0027/2011 Undisclosed Partnered with Par Pharma -- ANDA under review by FDA

    INT0020/2010 Insomnia -- in Pivotal Study

    INT0024/2010 Idiopathic pulmonary fibrosis -- in Pivotal Study

    INT0028/2011 Cancer pain (cannabinoid) --in Pivotal Study

    INT0030/2011 Animal health -- in Pivotal Study

    INT0031/2012 Benign prostatic hyperplasia --in Pivotal Study
    -

  • Unknown Gem with Brutal Upside Potential ...GLTA

    2 Big Drugs already under review by FDA another 1 NDA filing for "Best in Class" Potency Drug and 1 ANDA filing for CHF will follow within 6 months .

    NDA submission for our anti-migraine VersaFilm(TM) product had been accepted for review, with an FDA-assigned PDUFA date of February 3, 2014.
    (According to Merck's most recent annual report, sales of Maxalt(R) were $638 million in 2012.)

    IntelGenx Announces Submission of ANDA for Buprenorphine/Naloxone Sublingual Film Product for the Treatment of Opiate Addiction
    (According to IMS Health, U.S. retail sales of Suboxone(R) Sublingual Film were approximately $1.5 billion in 2012.)

    Only 20 M on the float ..IGXT has the Potential to hit $10++ within 2 Year ! GLTA

    Intelgenx (IGXT)

    Market Cap : $27 M
    Cash: $3 M
    Price:0.52

    Burn-Rate : $2 M a year
    Shares Out : 51 M ( 30 M shares are held by Investors )

    IGXT´s Monster Pipeline :

    Product ......Application......... Status of Development

    INT0004/2006 Antidepressant -- US launch in 4Q 2012

    INT0008/2007 Migraine -- PDUFA Date on Feb 3 2014

    INT0007/2006 Erectile Dysfunction -- NDA filing lin early 2014

    INT0001/2004 CHF (Coronary Heart Failure), Hypertension -- ANDA filing in early 2014

    INT0027/2011 Undisclosed Partnered with Par Pharma -- ANDA under review by FDA

    INT0020/2010 Insomnia -- in Pivotal Study

    INT0024/2010 Idiopathic pulmonary fibrosis -- in Pivotal Study

    INT0028/2011 Cancer pain (cannabinoid) --in Pivotal Study

    INT0030/2011 Animal health -- in Pivotal Study

    INT0031/2012 Benign prostatic hyperplasia --in Pivotal Study
    -

  • Reply to

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    by megapickm Nov 4, 2013 1:45 PM
    megapickm megapickm Nov 4, 2013 1:45 PM Flag

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    by megapickm Nov 4, 2013 1:45 PM
    megapickm megapickm Nov 4, 2013 1:45 PM Flag

    s

  • Reply to

    Test

    by megapickm Nov 4, 2013 1:45 PM
    megapickm megapickm Nov 4, 2013 1:45 PM Flag

    s

  • Reply to

    Test

    by megapickm Nov 4, 2013 1:45 PM
    megapickm megapickm Nov 4, 2013 1:45 PM Flag

    s

  • Reply to

    Test

    by megapickm Nov 4, 2013 1:45 PM
    megapickm megapickm Nov 4, 2013 1:45 PM Flag

    s

PFE
28.60+0.41(+1.43%)Oct 23 4:00 PMEDT

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