We use cookies to understand how you use our site and to improve your experience. This includes personalizing content and advertising. To learn more, click here. By continuing to use our site, you accept our use of cookies, revised Privacy Policy and Terms of Service.
You are being directed to ZacksTrade, a division of LBMZ Securities and licensed broker-dealer. ZacksTrade and Zacks.com are separate companies. The web link between the two companies is not a solicitation or offer to invest in a particular security or type of security. ZacksTrade does not endorse or adopt any particular investment strategy, any analyst opinion/rating/report or any approach to evaluating individual securities.
If you wish to go to ZacksTrade, click OK. If you do not, click Cancel.
The Zacks Analyst Blog Highlights: Novartis, J&J, Pfizer, Novo Nordisk and Glaxo
Read MoreHide Full Article
For Immediate Release
Chicago, IL –October 14, 2019 – Zacks.com announces the list of stocks featured in the Analyst Blog. Every day the Zacks Equity Research analysts discuss the latest news and events impacting stocks and the financial markets. Stocks recently featured in the blog include: Novartis (NVS - Free Report) , J&J (JNJ - Free Report) , Pfizer (PFE - Free Report) , Novo Nordisk (NVO - Free Report) and Glaxo (GSK - Free Report) .
Here are highlights from Friday’s Analyst Blog:
Pharma Stock Roundup: NVS, NVO, GSK and More
This week, the FDA approved Novartis’ potential blockbuster eye drug, Beovu. J&J submitted a regulatory application seeking label expansion approval of its plaque psoriasis drug, Stelara for pediatric patients. Pfizer, Novo Nordisk and Glaxo announced licensing deals.
Recap of the Week’s Most Important Stories
FDA Approves Novartis’ New Eye Drug:The FDA granted approval to Novartis’ ophthalmology drug, Beovu (brolucizumab) injection to treat wet age-related macular degeneration (AMD). Novartis claims that this anti-VEGF therapy offers greater fluid resolution as compared to Regeneron/Bayer’s market-leading drug Eylea. The FDA approval was based on data from the phase III HAWK and HARRIER studies, in which Beovu demonstrated significant advantages over Eylea.
Meanwhile, Novartis announced data from the phase IIb dose-finding study, which showed that more patients treated with its investigational monoclonal antibody, ligelizumab, were completely symptom-free from chronic spontaneous urticaria compared to Xolair (300 mg), which Novartis markets together with Roche.
J&J Files sBLA for Stelara in Adolescent Patients: J&J submitted a supplemental Biologics License Application (sBLA) to the FDA, seeking approval of Stelara for the treatment of pediatric patients (6 to 11 years of age) with moderate-to-severe plaque psoriasis. Stelara is already marked for adolescents and adults with moderate-to-severe plaque psoriasis. Stelara is also marketed to treat adults with active psoriatic arthritis and moderate-to-severe Crohn's disease.
Meanwhile, a Philadelphia jury ordered J&J to pay punitive damages of $8 billion to a man who claimed that the use of its antipsychotic drug, Risperdal caused him to develop breasts. The lawsuit filed by Nicholas Murray claimed that J&J did not warn of the risk that young men using Risperdal can develop enlarged breasts. J&J responded by saying that the award was “grossly disproportionate" and was confident that the jury verdict will be overturned in the court.
Pfizer, Glaxo and Novo Nordisk Sign New Deals:Pfizer in-licensed global rights to Akcea Therapeutics’ investigational antisense therapy AKCEA-ANGPTL3-LRx which is being evaluated in a phase II study as a treatment for patients with type II diabetes, hypertriglyceridemia and non-alcoholic fatty liver disease (NAFLD). AKCEA-ANGPTL3-LRx is designed to reduce the production of a protein in liver. Akcea is an affiliate of Ionis Pharmaceuticals and the companies will receive an upfront payment of $250 million from Pfizer, which will be split equally between the two companies. This apart, they will be entitled to milestone payments of up to $1.3 billion as well as royalties.
Novo Nordisk signed a three-year research deal with bluebird bio to develop in vivo genome editing candidates for hemophilia and other severe genetic diseases. Per the deal, bluebird bio’s new platform technology — mRNA-based megaTAL technology — will be utilized to create a highly differentiated approach to treat severe genetic diseases. No financial terms of the deal were disclosed.
Glaxo also announced a five-year collaboration with small biotech Lyell Immunopharma to develop next generation cancer cell therapies.
The NYSE ARCA Pharmaceutical Index rose 0.4% in the last five trading sessions.
Past performance is no guarantee of future results. Inherent in any investment is the potential for loss. This material is being provided for informational purposes only and nothing herein constitutes investment, legal, accounting or tax advice, or a recommendation to buy, sell or hold a security. No recommendation or advice is being given as to whether any investment is suitable for a particular investor. It should not be assumed that any investments in securities, companies, sectors or markets identified and described were or will be profitable. All information is current as of the date of herein and is subject to change without notice. Any views or opinions expressed may not reflect those of the firm as a whole. Zacks Investment Research does not engage in investment banking, market making or asset management activities of any securities. These returns are from hypothetical portfolios consisting of stocks with Zacks Rank = 1 that were rebalanced monthly with zero transaction costs. These are not the returns of actual portfolios of stocks. The S&P 500 is an unmanaged index. Visit http://www.zacks.com/performance for information about the performance numbers displayed in this press release.
See More Zacks Research for These Tickers
Normally $25 each - click below to receive one report FREE:
Image: Bigstock
The Zacks Analyst Blog Highlights: Novartis, J&J, Pfizer, Novo Nordisk and Glaxo
For Immediate Release
Chicago, IL –October 14, 2019 – Zacks.com announces the list of stocks featured in the Analyst Blog. Every day the Zacks Equity Research analysts discuss the latest news and events impacting stocks and the financial markets. Stocks recently featured in the blog include: Novartis (NVS - Free Report) , J&J (JNJ - Free Report) , Pfizer (PFE - Free Report) , Novo Nordisk (NVO - Free Report) and Glaxo (GSK - Free Report) .
Here are highlights from Friday’s Analyst Blog:
Pharma Stock Roundup: NVS, NVO, GSK and More
This week, the FDA approved Novartis’ potential blockbuster eye drug, Beovu. J&J submitted a regulatory application seeking label expansion approval of its plaque psoriasis drug, Stelara for pediatric patients. Pfizer, Novo Nordisk and Glaxo announced licensing deals.
Recap of the Week’s Most Important Stories
FDA Approves Novartis’ New Eye Drug:The FDA granted approval to Novartis’ ophthalmology drug, Beovu (brolucizumab) injection to treat wet age-related macular degeneration (AMD). Novartis claims that this anti-VEGF therapy offers greater fluid resolution as compared to Regeneron/Bayer’s market-leading drug Eylea. The FDA approval was based on data from the phase III HAWK and HARRIER studies, in which Beovu demonstrated significant advantages over Eylea.
Meanwhile, Novartis announced data from the phase IIb dose-finding study, which showed that more patients treated with its investigational monoclonal antibody, ligelizumab, were completely symptom-free from chronic spontaneous urticaria compared to Xolair (300 mg), which Novartis markets together with Roche.
J&J Files sBLA for Stelara in Adolescent Patients: J&J submitted a supplemental Biologics License Application (sBLA) to the FDA, seeking approval of Stelara for the treatment of pediatric patients (6 to 11 years of age) with moderate-to-severe plaque psoriasis. Stelara is already marked for adolescents and adults with moderate-to-severe plaque psoriasis. Stelara is also marketed to treat adults with active psoriatic arthritis and moderate-to-severe Crohn's disease.
Meanwhile, a Philadelphia jury ordered J&J to pay punitive damages of $8 billion to a man who claimed that the use of its antipsychotic drug, Risperdal caused him to develop breasts. The lawsuit filed by Nicholas Murray claimed that J&J did not warn of the risk that young men using Risperdal can develop enlarged breasts. J&J responded by saying that the award was “grossly disproportionate" and was confident that the jury verdict will be overturned in the court.
Pfizer, Glaxo and Novo Nordisk Sign New Deals:Pfizer in-licensed global rights to Akcea Therapeutics’ investigational antisense therapy AKCEA-ANGPTL3-LRx which is being evaluated in a phase II study as a treatment for patients with type II diabetes, hypertriglyceridemia and non-alcoholic fatty liver disease (NAFLD). AKCEA-ANGPTL3-LRx is designed to reduce the production of a protein in liver. Akcea is an affiliate of Ionis Pharmaceuticals and the companies will receive an upfront payment of $250 million from Pfizer, which will be split equally between the two companies. This apart, they will be entitled to milestone payments of up to $1.3 billion as well as royalties.
Novo Nordisk signed a three-year research deal with bluebird bio to develop in vivo genome editing candidates for hemophilia and other severe genetic diseases. Per the deal, bluebird bio’s new platform technology — mRNA-based megaTAL technology — will be utilized to create a highly differentiated approach to treat severe genetic diseases. No financial terms of the deal were disclosed.
Glaxo also announced a five-year collaboration with small biotech Lyell Immunopharma to develop next generation cancer cell therapies.
The NYSE ARCA Pharmaceutical Index rose 0.4% in the last five trading sessions.
Media Contact
Zacks Investment Research
800-767-3771 ext. 9339
support@zacks.com
http://www.zacks.com
Past performance is no guarantee of future results. Inherent in any investment is the potential for loss. This material is being provided for informational purposes only and nothing herein constitutes investment, legal, accounting or tax advice, or a recommendation to buy, sell or hold a security. No recommendation or advice is being given as to whether any investment is suitable for a particular investor. It should not be assumed that any investments in securities, companies, sectors or markets identified and described were or will be profitable. All information is current as of the date of herein and is subject to change without notice. Any views or opinions expressed may not reflect those of the firm as a whole. Zacks Investment Research does not engage in investment banking, market making or asset management activities of any securities. These returns are from hypothetical portfolios consisting of stocks with Zacks Rank = 1 that were rebalanced monthly with zero transaction costs. These are not the returns of actual portfolios of stocks. The S&P 500 is an unmanaged index. Visit http://www.zacks.com/performance for information about the performance numbers displayed in this press release.