Advertisement
Australia markets closed
  • ALL ORDS

    7,837.40
    -100.10 (-1.26%)
     
  • ASX 200

    7,575.90
    -107.10 (-1.39%)
     
  • AUD/USD

    0.6528
    +0.0005 (+0.08%)
     
  • OIL

    83.45
    -0.12 (-0.14%)
     
  • GOLD

    2,342.80
    +0.30 (+0.01%)
     
  • Bitcoin AUD

    97,921.95
    +825.00 (+0.85%)
     
  • CMC Crypto 200

    1,330.21
    -66.32 (-4.74%)
     
  • AUD/EUR

    0.6109
    +0.0036 (+0.60%)
     
  • AUD/NZD

    1.0989
    +0.0031 (+0.29%)
     
  • NZX 50

    11,805.09
    -141.34 (-1.18%)
     
  • NASDAQ

    17,749.01
    +318.50 (+1.83%)
     
  • FTSE

    8,140.36
    +61.50 (+0.76%)
     
  • Dow Jones

    38,238.24
    +152.44 (+0.40%)
     
  • DAX

    18,170.95
    +253.67 (+1.42%)
     
  • Hang Seng

    17,651.15
    +366.61 (+2.12%)
     
  • NIKKEI 225

    37,934.76
    +306.28 (+0.81%)
     

Novartis' (NVS) Beovu Gets FDA Approval for Label Update

Novartis AG NVS announced that the FDA has approved a label update for ophthalmology drug, Beovu (brolucizumab), to include additional safety information regarding retinal vasculitis and retinal vascular occlusion.

The update to the label includes the addition of a sub-section dedicated to retinal vasculitis and/or retinal vascular occlusion under ‘Warnings and Precautions.’ It also specifies that these adverse reactions are part of a spectrum of intraocular inflammation rates from the phase III HAWK & HARRIER studies.

The label update comes after Novartis decided to evaluate post-marketing cases reported as severe vision loss, retinal artery occlusion and/or vasculitis with Beovu.

Thereafter, the company initiated its own internal review of these post-marketing safety case reports, including the establishment of an external Safety Review Committee (SRC). The SRC recently issued a report of its unmasked, independent analysis of HAWK & HARRIER adverse events, wherein it found that cases similar to those reported post marketing were present in the HAWK & HARRIER clinical studies.

ADVERTISEMENT

We remind investors that Beovu was approved by the FDA in 2019 for the treatment of wet age-related macular degeneration (AMD), based on findings from the late-stage HAWK and HARRIER studies, in which the drug demonstrated non-inferiority compared to Regeneron REGN and Bayer’s BAYRY Eylea.

The drug was touted to pose stiff competition to Eylea and Roche’s RHHBY Lucentis with its less frequent dosing schedule. However, a few cases of vasculitis casted a shadow on the drug’s safety profile.

The stock has lost 4.8% in the year so far against the industry’s gain of 1.3%.

 

After having gone through a series of restructuring moves, Novartis looks to strengthen its core pharma business. Solid performance of key drugs like Cosentyx and Entresto and contributions from gene therapy, Zolgensma, have boosted performance, lately.

New launches like Piqray and Beovu too were projected to boost growth. However, it remains to be seen the growth trajectory Beovu takes up following this label update.

Novartis currently carries a Zacks Rank #3 (Hold). You can see the complete list of today’s Zacks #1 Rank (Strong Buy) stocks here.

5 Stocks Set to Double

Each was hand-picked by a Zacks expert as the #1 favorite stock to gain +100% or more in 2020. Each comes from a different sector and has unique qualities and catalysts that could fuel exceptional growth.

Most of the stocks in this report are flying under Wall Street radar, which provides a great opportunity to get in on the ground floor.

Today, See These 5 Potential Home Runs >>


Want the latest recommendations from Zacks Investment Research? Today, you can download 7 Best Stocks for the Next 30 Days. Click to get this free report
 
Regeneron Pharmaceuticals, Inc. (REGN) : Free Stock Analysis Report
 
Roche Holding AG (RHHBY) : Free Stock Analysis Report
 
Novartis AG (NVS) : Free Stock Analysis Report
 
Bayer Aktiengesellschaft (BAYRY) : Free Stock Analysis Report
 
To read this article on Zacks.com click here.
 
Zacks Investment Research