Rainbow Rare Earths Phalaborwa project shaping up to be one of the lowest cost producers globally. Watch the video here.

Less Ads, More Data, More Tools Register for FREE

Pin to quick picksAllergy Thera. Regulatory News (AGY)

Share Price Information for Allergy Thera. (AGY)

London Stock Exchange
Share Price is delayed by 15 minutes
Get Live Data
Share Price: 5.25
Bid: 5.00
Ask: 5.50
Change: 0.00 (0.00%)
Spread: 0.50 (10.00%)
Open: 5.24
High: 5.50
Low: 5.24
Prev. Close: 5.25
AGY Live PriceLast checked at -

Watchlists are a member only feature

Login to your account

Alerts are a premium feature

Login to your account

Regulatory and Trading Update

25 Apr 2019 07:00

RNS Number : 0195X
Allergy Therapeutics PLC
25 April 2019
 

 

 

 

Allergy Therapeutics plc

("Allergy Therapeutics" or the "Group")

 

Regulatory and Trading Update

 

- Successful FDA and Paul Ehrlich Institut meetings on design of Phase III PQ Grass trial, now planned to commence in H2 2020

 

25 April 2019 Allergy Therapeutics plc (AIM: AGY), the fully integrated commercial biotechnology company specialising in allergy vaccines, today announces the outcome of successful discussions with the Paul Ehrlich Institut (PEI) in Germany and the Food and Drug Administration (FDA) in the US regarding the pivotal Phase III PQ Grass trial design. The trial, being planned for the US and Europe, will evaluate the efficacy and safety of the Group's short course, aluminium-free pre-seasonal immunotherapy in the prevention of the symptoms of allergic rhinoconjunctivitis caused by grass pollen.

 

The Group presented positive results from its Phase II PQ Grass trial to the PEI and FDA and agreement was reached on the dose to progress into Phase III, as well as other essential features of the trial design. Accordingly, in order to finalise the design of the trial and incorporate the latest clinical evidence, the trial is expected to commence in H2 2020, to be aligned with the 2020/2021 allergy season.

 

The Group continues to make good progress with its broad clinical pipeline. A readout of the Phase I Acarovac MPL trial for house dust mite allergies is expected in Q2 2019. Manufacturing scale-up of the Group's Polyvac Peanut product, which is critical to ensure commercial manufacture in a consistent manner for clinical trials and in GMP conditions, is progressing well. The Phase I first-in-human trial for Polyvac Peanut is now expected in H1 2020 as we complete the pre-clinical work in advance of human dosing next year.

 

The commercial business continues to trade in line with market expectations and gain market share, and the Group remains well-funded to progress its commercial and clinical programme into 2021. As announced in the 6 March 2019 Interim Results, the Group had a cash balance of £31.6m at 31 December 2018.

 

Manuel Llobet, CEO at Allergy Therapeutics, stated: "With the positive outcomes from our meetings with the FDA and Paul Ehrlich Institut, we have agreed design of our Phase III PQ Grass trial, including patient number requirements and statistical measures.

 

"Given the sensitivity of clinical trials in allergic rhinitis to the subjective nature of patient-reported outcomes, it is important that we incorporate any potential learnings from our recent trials into the final trial design for PQ Grass. Given the PQ Grass trial is expected to commence in H2 2020 we are confident that we have time to amend the protocol accordingly if required. This product has the potential to become a much-needed treatment option for the estimated 25-30% of the EU and US populations who are allergic to grass pollen1, and we believe that the PQ Grass trial will enable us to demonstrate the efficacy of this short-course grass pollen immunotherapy.

 

"The potential of our pipeline is illustrated by the expected newsflow from our other clinical portfolio programmes and we look forward to updating the market as these progress."

 

 

This announcement contains inside information for the purposes of Article 7 of Regulatory (EU) No596/2014.

- ENDS -

 

 

 

For further information, please contact:

 

Allergy Therapeutics

+44 (0) 1903 845 820

Manuel Llobet, Chief Executive Officer

Nick Wykeman, Chief Financial Officer

 

Panmure Gordon

+44 (0) 20 7886 2500

Freddy Crossley, Emma Earl, Corporate Finance

Erik Anderson, Corporate Broking

 

Consilium Strategic Communications

+44 20 3709 5700

Mary-Jane Elliott / David Daley / Nicholas Brown / Olivia Manser

allergytherapeutics@consilium-comms.com

 

Stern Investor Relations, Inc.

+1 212 362 1200

Christina Tartaglia

christina@sternir.com

 

Notes for editors:

 

About Allergy Therapeutics

 

Allergy Therapeutics is an international commercial biotechnology company focussed on the treatment and diagnosis of allergic disorders, including aluminium free immunotherapy vaccines that have the potential to cure disease. The Group sells proprietary and third-party products from its subsidiaries in nine major European countries and via distribution agreements in an additional ten countries. Its broad pipeline of products in clinical development include vaccines for grass, tree and house dust mite, and peanut allergy vaccine in pre-clinical development. Adjuvant systems to boost performance of vaccines outside allergy are also in development.

 

Formed in 1999 out of Smith Kline Beecham, Allergy Therapeutics is headquartered in Worthing, UK with more than 11,000m2 of state-of-the-art MHRA-approved manufacturing facilities and laboratories. The Group, which has achieved double digit compound annual growth since formation, employs c.500 employees and is listed on the London Stock Exchange (AIM:AGY). For more information, please see www.allergytherapeutics.com.

 

 

About Grass MATA MPL

 

Grass MATA MPL contains three distinct components: allergoids, micro-crystalline tyrosine (MCT) and monophosphoryl lipid A (MPL®). Allergoids (natural allergens chemically modified to form allergoids) exhibit reduced allergenicity that improves safety and allows for delivery of higher doses. These are combined with the depot adjuvant technology MCT to provide enhanced immune exposure and further improved tolerability.

 

Finally, the immune response is enhanced and directed by the adjuvant MPL®. MPL is a toll-like 4 receptor (TLR4) agonist which has been extensively used in the Group's other allergy vaccines available on the market and in vaccines registered in the USA.

 

If approved, the product will be the first registered subcutaneous immunotherapy product in the US for grass allergy.

 

 

About US Allergy Market

 

The US allergy immunotherapy market, which is anticipated to be the main market for this product, is estimated by the Group to be worth $2 billion with potential peak grass vaccine sales of $300-400 million per annum.

 

1- European Academy of Allergy and Clinical Immunology (EAACI) Global Atlas of Allergy. 2014.

 

This information is provided by RNS, the news service of the London Stock Exchange. RNS is approved by the Financial Conduct Authority to act as a Primary Information Provider in the United Kingdom. Terms and conditions relating to the use and distribution of this information may apply. For further information, please contact rns@lseg.com or visit www.rns.com.
 
END
 
 
MSCEAFLLADDNEAF
Date   Source Headline
13th Nov 20084:54 pmRNSHolding(s) in Company
28th Oct 200810:19 amRNSAnnual Report and Accounts
29th Sep 200810:46 amRNSHolding(s) in Company
22nd Sep 20087:00 amRNSFinal Results
22nd Sep 20087:00 amRNSResearch Update
22nd Aug 20083:06 pmRNSHolding(s) in Company
9th Jun 20087:00 amRNSResearch Update
14th May 20087:00 amRNSResearch Update
7th May 200811:50 amRNSDirector/PDMR Shareholding
15th Apr 20082:28 pmRNSAIM Notice 26
17th Mar 20087:01 amRNSInterim Results
14th Mar 200811:59 amRNSHolding(s) in Company
7th Mar 20081:47 pmRNSHolding(s) in Company
31st Jan 20087:00 amRNSNotice of Results
29th Jan 20084:15 pmRNSHolding(s) in Company - Amend
29th Jan 200812:42 pmRNSHolding(s) in Company
14th Jan 20087:01 amRNSChange of Adviser
27th Dec 200710:21 amRNSGrant of Options
12th Dec 200710:28 amRNSAvailability of Annual Report
29th Nov 20072:22 pmRNSResult of AGM
16th Nov 20073:31 pmRNSDirector/PDMR Shareholding
9th Nov 20073:24 pmRNSHolding(s) in Company
1st Nov 20077:02 amRNSResearch Update
29th Oct 20073:39 pmRNSHolding(s) in Company
26th Oct 20073:10 pmRNSDirector/PDMR Shareholding
11th Oct 200710:33 amRNSHolding(s) in Company
25th Sep 20077:00 amRNSFinal Results
14th Aug 20078:00 amRNSChange of Adviser
10th Aug 20079:28 amRNSAIM Rule 26
6th Aug 200711:03 amRNSHolding(s) in Company
24th Jul 200710:41 amRNSResearch Update
17th Jul 20073:36 pmRNSHolding(s) in Company
11th Jul 200710:01 amRNSClinical Update
19th Jun 200711:03 amRNSHolding(s) in Company
14th Jun 20077:01 amRNSResearch Update
8th Jun 20076:00 pmRNSAppointment of Joint Broker
29th May 20079:15 amRNSEur40 million Debt Facility
29th May 20077:02 amRNSEUR40 million Debt Facility
8th May 200710:45 amRNSHolding(s) in Company
18th Apr 20077:01 amRNSResearch Update
2nd Apr 20077:02 amRNSResearch Update
23rd Mar 200711:42 amRNSHolding(s) in Company
23rd Mar 20077:01 amRNSRe Investment
5th Mar 200712:04 pmRNSHolding(s) in Company
28th Feb 20077:01 amRNSInterim Results
27th Feb 200710:21 amRNSHolding(s) in Company
15th Feb 20072:29 pmRNSHolding(s) in Company
6th Feb 20074:46 pmRNSHolding(s) in Company
5th Feb 20073:04 pmRNSHolding(s) in Company
31st Jan 200710:18 amRNSTotal Voting Rights

Due to London Stock Exchange licensing terms, we stipulate that you must be a private investor. We apologise for the inconvenience.

To access our Live RNS you must confirm you are a private investor by using the button below.

Login to your account

Don't have an account? Click here to register.

Quickpicks are a member only feature

Login to your account

Don't have an account? Click here to register.