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First Patient in Pivotal Phase III Birch Study

16 Mar 2017 07:00

RNS Number : 6158Z
Allergy Therapeutics PLC
16 March 2017
 

 

 

Allergy Therapeutics plc

("Allergy Therapeutics" or the "Company")

 

First Patient Recruited in Pivotal Phase III Birch Immunotherapy B301 Study

 

 

16 March 2017 Allergy Therapeutics (AIM:AGY), the fully integrated specialty pharmaceutical company specialising in allergy vaccines, today announces the recruitment of the first patient in its Phase III study designed to evaluate the efficacy and safety of its ultra-short course, aluminium-free Pollinex® Quattro Birch immunotherapy to address the cause of symptoms of allergic rhinoconjunctivitis due to birch pollen.

 

The first patient in the B301 Phase III study was recruited in Austria on 15 March. The study is anticipated to run for one year and involve more than 550 patients over 50 sites across Germany, Sweden, Austria and Poland. The primary objective of this study is to evaluate the efficacy of Pollinex® Quattro Birch in birch pollen-induced rhinoconjunctivitis and to enable registration of the product in Germany via the Therapieallergene-Verordnung (TAV) process of the Paul Ehrlich Institut, before anticipated marketing authorisation in 2019.

 

The adopted cumulative dose has been demonstrated to be efficacious in two recent dose range finding studies with respect to reduction of symptoms induced by a conjunctival provocation test (CPT) with no prior safety concerns.

 

Manuel Llobet, Chief Executive Officer of Allergy Therapeutics, said: "The start of our Phase III trial investigating Pollinex Quattro Birch marks the beginning of a number of trials aimed at strengthening our product portfolio across Europe and helping the 6% of Europeans who test positive to birch allergens. If approved, Pollinex Quattro Birch will be the first MPL adjuvanted ultra-short course aluminium-free vaccine ever approved. Combined with our clinical programme in the US focusing on Pollinex Quattro Grass, we aim to have a comprehensive global modified allergen + MCT® and MPL vaccine package that focuses on delivering convenience, safety, efficacy and enhanced patient compliance."

 

For further information, please contact:

 

Allergy Therapeutics

+44 (0) 1903 845 820

Manuel Llobet, Chief Executive Officer

Nick Wykeman, Finance Director

 

Panmure Gordon

+44 (0) 20 7886 2500

Freddy Crossley / Duncan Monteith, Corporate Finance

Tom Salvesen, Corporate Broking

 

Consilium Strategic Communications

+44 20 3709 5700

Mary-Jane Elliott / Ivar Milligan

allergytherapeutics@consilium-comms.com

 

Notes for editors:

 

About Allergy Therapeutics

Allergy Therapeutics is an international specialty pharmaceutical company focussed on the treatment and diagnosis of allergic disorders including immunotherapy vaccines that cure disease. The Company sells proprietary products and third party products from its subsidiaries in nine major European countries and via distribution agreements in an additional ten countries.

 

Formed in 1999 out of Smith Kline Beecham, Allergy Therapeutics is headquartered in Worthing, UK with MHRA-approved manufacturing facilities. The Company employs c.495 employees and is listed on the London Stock Exchange (AIM:AGY). For more information, please see www.allergytherapeutics.com.

 

About Pollinex Quattro Birch

Pollinex Quattro Birch is a unique ultra-short course allergen-specific immunotherapy comprising three key technologies tailored to reduce irritation and systemic reactions, namely: modified allergens, microcrystalline tyrosine (MCT®) and monophosphoryl lipid A (MPL).

 

The ultra-short duration of treatment is achieved via allergen modification that transforms the structure of birch allergens to allow increased doses to be delivered compared to traditional unmodified preparations. The potent depot adjuvant, MCT®, has a Th1 immuno-modulating action that acts in synergy with the TLR4 receptor agonist MPL to augment a shift in the immune reactions responsible for the symptoms of allergic rhinitis.

 

 

About Allergic Rhinitis

Allergic rhinitis and conjunctivitis affects between 10% and 30% of the population worldwide1. Symptoms can be intrusive and debilitating and can include watery eyes, runny nose and inflammation. Current first line treatments such as antihistamines and corticosteroids lead to insufficient symptom control and add to the economic and patient burden. Currently, specific immunotherapy is the only known treatment that addresses the underlying cause of symptoms.

References

1. World Health Organization. White Book on Allergy 2011-2012 Executive Summary. By Prof. Ruby Pawankar, MD, PhD, Prof. Giorgio Walkter Canonica, MD, Prof. Stephen T. Holgate, BSc, MD, DSc, FMed Sci and Prof. Richard F. Lockey, MD.

This information is provided by RNS
The company news service from the London Stock Exchange
 
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RESDBGDXCXBBGRU
Date   Source Headline
31st Jan 20187:00 amRNSTrading Update
10th Jan 20183:19 pmRNSHoldings in Company
9th Jan 20187:00 amRNSPQ Birch Phase III trial completes recruitment
12th Dec 20177:00 amRNSCo-development agreement with Ergomed plc
7th Dec 20175:08 pmRNSHolding(s) in Company
22nd Nov 201711:36 amRNSResult of AGM
21st Nov 20177:00 amRNSBlock Listing Application
13th Nov 20177:00 amRNSAllergy Therapeutics to Present at Jefferies 2017
7th Nov 201712:59 pmRNSDirector/PDMR Shareholding
7th Nov 201711:54 amRNSDirector/PDMR Shareholding
19th Oct 20174:14 pmRNSPublication of Annual Report and notice of AGM
19th Oct 20177:00 amRNSCommencement of dosing in PQ Grass Phase II Trial
12th Oct 20175:39 pmRNSHolding(s) in Company
12th Oct 20172:55 pmRNSDirector/PDMR Shareholding
10th Oct 20177:15 amRNSHardman Research: Continuing to gain market share
28th Sep 20177:00 amRNSPreliminary Results
18th Sep 20177:00 amRNSApproval for PQ Grass Phase II trial
11th Sep 20177:00 amRNSExpansion of Clinical Development and R&D teams
15th Aug 20177:00 amRNSNotice of Results
18th Jul 20177:00 amRNSTrading Update
6th Jul 20177:00 amRNSPublication of adjuvant studies in journals
27th Jun 20177:00 amRNSInvestor and analyst site visits
19th Jun 20177:00 amRNSSatellite Symposium at EAACI 2017
6th Jun 20177:00 amRNSDirectorate changes
2nd Jun 201712:55 pmRNSHolding(s) in Company
13th Apr 20177:00 amRNSIssue of Equity
5th Apr 20177:15 amRNSHardman Research: Development across portfolio
29th Mar 20177:00 amRNSInterim Results for six months ended 31 Dec 2016
16th Mar 20177:00 amRNSFirst Patient in Pivotal Phase III Birch Study
9th Mar 20177:00 amRNSNotice of Interim Results
14th Feb 20177:00 amRNSHouse Dust Mite Allergy Vaccine Gains CTA Approval
8th Feb 20177:00 amRNSDirectorate Change
1st Feb 20177:00 amRNSPositive Efficacy & Safety Data in Peanut Vaccine
20th Jan 20177:15 amRNSHardman Research: Investment driving market share
19th Jan 20177:00 amRNSTrading Update
30th Dec 20162:31 pmRNSGrant of Awards
24th Nov 20165:23 pmRNSResult of AGM
2nd Nov 20167:00 amRNSEU Patent Office grants patent for MCT
27th Oct 20161:10 pmRNSIssue of equity in respect of exercise of options
24th Oct 20161:35 pmRNSAnnual Report and Accounts
10th Oct 20167:00 amRNSNew data from novel adjuvant system
3rd Oct 201611:28 amRNSIssue of equity in respect of exercise of options
29th Sep 201612:40 pmRNSDirector/PDMR Shareholding
28th Sep 20167:00 amRNSDirector/PDMR Shareholding
26th Sep 201611:59 amRNSDirector/PDMR Shareholding
26th Sep 201610:46 amRNSHardman Research: Performance drives market share
26th Sep 20167:00 amRNSAllergy Therapeutics Preliminary Results
20th Sep 20164:58 pmRNSIssue of equity in respect of exercise of options
5th Sep 20167:00 amRNSNotice of Preliminary Results
13th Jul 20167:00 amRNSTrading Update

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