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Last 26.75 GBp
Change Today +1.50 / 5.94%
Volume 290.0K
AGY On Other Exchanges
Symbol
Exchange
London
OTC US
Berlin
As of 11:30 AM 09/3/15 All times are local (Market data is delayed by at least 15 minutes).

allergy therapeutics plc (AGY) Snapshot

Open
25.25 GBp
Previous Close
25.25 GBp
Day High
26.88 GBp
Day Low
25.25 GBp
52 Week High
08/4/15 - 27.75 GBp
52 Week Low
10/16/14 - 17.75 GBp
Market Cap
146.0M
Average Volume 10 Days
33.6K
EPS TTM
0.0057 GBp
Shares Outstanding
545.8M
EX-Date
--
P/E TM
46.9x
Dividend
--
Dividend Yield
--
Current Stock Chart for ALLERGY THERAPEUTICS PLC (AGY)

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allergy therapeutics plc (AGY) Details

Allergy Therapeutics plc, a specialty pharmaceutical company, develops, manufactures, markets, and sells pharmaceutical vaccine products for the immunological treatment of allergic conditions primarily in Europe. The company’s primary flagship product consists of the Pollinex Quattro for the treatment of allergic conditions; and monophosphoryl-lipid A, a substance, which enhances the immune response to an antigen or allergen. It offers sublingual product, including Oralvac Compact; Venomil product, which is used for the wasp and bee treatment; probiotic products, such as Kallergen-Th, ATI Prob, and Pollagen; Acarovac Plus, a novel tyrosine-adsorbed, modified-allergen product developed for treatment of perennial mite allergy; and DAP, a product for use in the diagnosis of type I or immediate hypersensitivity to benzylpenicillin and related antibiotics (betalactams) by means of cutaneous tests (prick and intradermal). The company markets its products under various brands, including Pollinex Quattro, Polligoid, and TA Gräser Top. Allergy Therapeutics plc was founded in 1934 and is headquartered in Worthing, the United Kingdom.

345 Employees
Last Reported Date: 09/24/14
Founded in 1934

allergy therapeutics plc (AGY) Top Compensated Officers

Chief Executive Officer and Executive Directo...
Total Annual Compensation: 291.0K GBP
Finance Director, Company Secretary and Direc...
Total Annual Compensation: 192.8K GBP
Compensation as of Fiscal Year 2014.

allergy therapeutics plc (AGY) Key Developments

Allergy Therapeutics plc Provides Revenue Guidance for the Full Year Ended June 30, 2015

Allergy Therapeutics plc provided revenue guidance for the full year ended June 30, 2015. The company expects to report revenue growth of 11% for the year at constant currency, reflecting revenues of approximately £46.6 million. This double digit growth rate in a flat market demonstrates that Allergy Therapeutics has outperformed the market, gaining market share of approximately 1% a year. These gains have occurred in all of the company's key markets, making Allergy Therapeutics the outstanding performer in Europe in this competitive area. Reported revenues are expected to be approximately £43.2 million, slightly ahead of analyst expectations, representing growth of 3%, despite the negative impact from the weakening Euro.

Allergy Therapeutics Announces Positive Results from its Prospective Observational Acarovac Plus Clinical Study

Allergy Therapeutics announced positive results from its prospective observational Acarovac Plus clinical study for the treatment of house dust mite allergy. Acarovac Plus is being developed as one of the Company's new generation of products to address the perennial allergy market with innovative and short-course therapies. At the Adjuvants in Allergy conference over the past weekend, Dr. Albert Roger, Director of the Allergy Unit at Universitari Hospital Germans Trias Pujol, Badalona Spain, presented the results of a prospective observational one-year follow-up study, comparing the safety, tolerability and long-term effectiveness of Acarovac Plus using Dermatophagoides pteronyssinus (house dust mite) in 30 adult patients with allergic rhinitis and/or asthma. Acarovac Plus has been designed to administer maintenance doses every 6-8 weeks, reducing the number of annual injections required and providing a natural, biodegradable, alternative depot vaccine. Tolerability of Acarovac Plus was demonstrated with no reported adverse events. The effectiveness of Acarovac Plus was measured in patients using a nasal provocation test, which evaluates the sensitivity of each patient to mite allergens. Nasal airway assessments were performed using peak nasal inspiratory flow measurements. In summary, a reduction in symptom scores of >50% were observed during follow up visits after one year. Immunological markers were also assessed and showed significant improvements in antibody IgG4 and anti-inflammatory IL-10 molecules, indicating tolerance induction in patients after one year of treatment. A validated patient satisfaction survey provided information that was reflective of the clinical findings from the study. A high degree of overall patient satisfaction was observed, which encompassed significant improvements in scores after one year in relation to overall effectiveness and convenience of the treatment. This reinforces one of the main objectives of Allergy Therapeutics in improving patient life by producing effective treatments, while at the same time reducing the discomfort of injections, improving compliance and adherence of allergy immunotherapy products. Further to the efficacy noted for Acarovac Plus, Allergy Therapeutics is developing Acarovac Quattro, an ultra-short course therapy utilising the adjuvant monophosphoryl lipid A (MPL), which is used in the Company's successful Pollinex Quattro product range currently in late stage development in Europe and the US.

Allergy Therapeutics plc to Resume US Clinical Programme

Allergy Therapeutics announced that following productive discussions with the US Food and Drug Administration regarding the US clinical development of Pollinex® Quattro Grass MATA MPL, the Company has submitted its clinical trial protocols to the FDA. The trials are scheduled to start in September 2015. In addition, the company has engaged Inflamax Research Inc., the contract research organisation specialising in mobile environmental exposure chambers, to run the studies. Pollinex Quattro Grass could be the first subcutaneous seasonal allergy treatment to receive regulatory approval in the US, as well as being the Company's first product to be approved for the US market. The US allergy immunotherapy market is estimated to be CAD 2 billion. The company is resuming its clinical development programme of Pollinex Quattro Grass in the US following successful Phase I, II and III programmes, having invested $100 million to date in its Pollinex Quattro product pipeline. The company anticipates that it will submit a Biological Licence Application for Pollinex Quattro Grass for US regulatory approval in 2018, assuming the successful completion of the remaining clinical development programme. Following input on trial design from the FDA, the Company will initially conduct a small safety study, immediately followed by a Phase IIb study this year, before progressing into a pivotal Phase III study in 2016.

 

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Valuation AGY Industry Range
Price/Earnings 64.9x
Price/Sales 2.6x
Price/Book 5.2x
Price/Cash Flow 74.4x
TEV/Sales 3.1x
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