Advertisement
UK markets closed
  • FTSE 100

    8,433.76
    +52.41 (+0.63%)
     
  • FTSE 250

    20,645.38
    +114.08 (+0.56%)
     
  • AIM

    789.87
    +6.17 (+0.79%)
     
  • GBP/EUR

    1.1622
    +0.0011 (+0.09%)
     
  • GBP/USD

    1.2525
    +0.0001 (+0.01%)
     
  • Bitcoin GBP

    48,462.85
    -1,727.44 (-3.44%)
     
  • CMC Crypto 200

    1,257.62
    -100.39 (-7.39%)
     
  • S&P 500

    5,222.68
    +8.60 (+0.16%)
     
  • DOW

    39,512.84
    +125.08 (+0.32%)
     
  • CRUDE OIL

    78.20
    -1.06 (-1.34%)
     
  • GOLD FUTURES

    2,366.90
    +26.60 (+1.14%)
     
  • NIKKEI 225

    38,229.11
    +155.13 (+0.41%)
     
  • HANG SENG

    18,963.68
    +425.87 (+2.30%)
     
  • DAX

    18,772.85
    +86.25 (+0.46%)
     
  • CAC 40

    8,219.14
    +31.49 (+0.38%)
     

Atara Reports Initial Data for Multiple Sclerosis Candidate

Atara Biotherapeutics, Inc. ATRA announced initial ATA188 phase I safety results for patients with progressive multiple sclerosis (MS) at the 5th Congress of the European Academy of Neurology (EAN) in Oslo, Norway. The primary objective of the ongoing ATA188 phase I, dose-escalating clinical study is to evaluate safety and tolerability for patients with progressive MS.

ATA188 is a T-cell immunotherapy targeting Epstein-Barr virus (EBV) antigens, believed to be important for the potential treatment of MS.  MS is a chronic autoimmune, inflammatory disease that affects axons in the central nervous system (CNS).

Shares of the company have plunged 42.2% year to date against the industry’s growth of 5.7%.

Initial safety results, as of Apr 8, 2019, showed that the first three ATA188 dose cohorts were well tolerated, with no dose-limiting toxicities and no ≥3 grade treatment-related, treatment-emergent adverse events. The key secondary endpoints of the phase I study include measures of clinical improvement, such as expanded disability status scale (EDSS), MRI imaging and other clinical activity measures. The study is ongoing and aims to identify a recommended phase II dose (RP2D). Further, a phase Ib extension period for this study, using the RP2D, is now planned following the completion of the open-label, dose-escalation period.

ADVERTISEMENT

MS is a crowded market, with many companies already having drugs in their portfolio approved for this indication. Biogen, Inc. BIIB holds a strong position in this market with a wide range of products, including Avonex, Tysabri, Tecfidera and Plegridy. In March, swiss pharma giant Novartis AG NVS received FDA approval for its pipeline candidate Mayzent (siponimod), a next generation, selective sphingosine 1-phosphate receptor modulator, for the treatment of adults with relapsing forms of MS. Also Celgene’s CELG ozanimod, being developed for the treatment of people with relapsing forms of MS, is under review in the United States and Europe.

Zacks Rank

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

The Hottest Tech Mega-Trend of All

Last year, it generated $8 billion in global revenues. By 2020, it's predicted to blast through the roof to $47 billion. Famed investor Mark Cuban says it will produce "the world's first trillionaires," but that should still leave plenty of money for regular investors who make the right trades early.

See Zacks' 3 Best Stocks to Play This Trend >>


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
 
Novartis AG (NVS) : Free Stock Analysis Report
 
Atara Biotherapeutics, Inc. (ATRA) : Free Stock Analysis Report
 
Biogen Inc. (BIIB) : Free Stock Analysis Report
 
Celgene Corporation (CELG) : Free Stock Analysis Report
 
To read this article on Zacks.com click here.
 
Zacks Investment Research