(VEC) Vectura Group
Summary
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| 01-02-12 | RNS |
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RNS Number : 5389W Vectura Group plc 01 February 2012 Vectura Group plc (the "Company")
VOTING RIGHTS AND CAPITAL
Chippenham, UK, 1 February 2012: In accordance with the Financial Service Authority's Transparency Directive, Transitional Provision 6, Vectura Group plc (LSE: VEC) ("the Company") wishes to notify the market of the following:
The Company's issued share capital as at 31 January 2012 consists of 331,243,457 ordinary shares (previously, 331,155,557 ordinary shares as at 30 December 2011). The Company does not hold any ordinary shares in Treasury.
Therefore, the total number of ordinary shares in the Company with voting rights is 331,243,457.
The above figure of 331,243,457 ordinary shares may be used by shareholders as the denominator for the calculations by which they will determine if they are required to notify their interest in, or a change to their interest in, the Company under the Financial Service Authority's Disclosure and Transparency Rules.
Enquiries:
This information is provided by RNS The company news service from the London Stock Exchange More |
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| 26-01-12 | RNS |
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RNS Number : 1980W Vectura Group plc 26 January 2012 Vectura Group plcCancellation of Share PremiumChippenham, UK, 26 January 2012: Vectura Group plc (LSE: VEC) ("the Company"), is pleased to announce that further to the passing by its shareholders of the relevant resolution at the Company's last annual general meeting, held on 22 July 2011, the High Court of Justice in England and Wales yesterday made an order (the "Order") confirming the cancellation of substantially all of the Company's share premium account (the "Reduction"). The Reduction became effective on 25 January 2012 following the registration of the Order with the Registrar of Companies.
Enquiries:
This information is provided by RNS The company news service from the London Stock Exchange More |
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| 13-01-12 | RNS |
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RNS Number : 4973V Vectura Group plc 13 January 2012 Vectura Group Plc
Annual Information Update
Chippenham, UK, 13 January 2012: Vectura Group plc (the 'Company') (LSE: VEC) is pleased to provide its Annual Information Update in accordance with the requirements of Prospectus Rule 5.2.1R. This update relates to information that has been published or made available by the Company to the public in compliance with laws and rules dealing with the regulation of securities and the securities market in the 12 months up to and including 30 December 2011.
1. RNS Announcements
The following UK regulatory announcements have been made via the Regulatory News Service provided by the London Stock Exchange:
Copies of these regulatory announcements can be found on the Press Release Archive pages on the Company's website at www.vectura.com, or on the London Stock Exchange's website www.londonstockexchange.com.
The poll results for the resolutions put to the Company's Annual General Meeting held on 22 July 2011 were filed on the same day with the Financial Services Authority at uk.nsm@morningstar.com. This document is also available on the Company's website www.vectura.com, or on application to the Company Secretary.
2. Documents filed at Companies House
The Company has also made the following filings at Companies House:
3 November 2011 Form SH01 - Return of Allotment of Shares 30 November 2011 Form SH01 - Return of Allotment of Shares
Copies of the above documents, filed with the Registrar of Companies, may be obtained from Companies House, Crown Way, Cardiff CF14 3UZ, or through Companies House Direct at www.direct.companieshouse.gov.uk.
3. Documents published and sent to Shareholders
The Company's Annual Report and Accounts for the year ended 31 March 2011 and its Interim Report for the six-months ended 30 September 2011 were sent to, or made available to, Shareholders on 28 June 2011 and 16 December 2011 respectively. Copies of these reports are available on the Company's website at www.vectura.com.
4. In accordance with Article 27.30 of the Prospectus Directive, we confirm that the information referred to in this update was up-to-date at the time the information was published, but it is acknowledged that such disclosure may, at any time, become out-of-date due to changing circumstances.
Further information about Vectura and its activities can be found on the Company's website at www.vectura.com.
- Ends -
Enquiries:
This information is provided by RNS The company news service from the London Stock Exchange More |
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| 11-01-12 | RNS |
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RNS Number : 3346V Vectura Group plc 11 January 2012 Vectura Group plc - Interim Management StatementChippenham, UK - 11 January 2012: Vectura Group plc (LSE: VEC) ("Vectura"), the Company that specialises in developing inhaled therapies for the treatment of respiratory diseases, today publishes its Interim Management Statement for the period 01 October 2011 to date. Following the release in November of our interim results for the six months to 30 September 2011, in which we posted revenues of £21.1m, profit after tax of £2.6m and cash of £80.2m (£74.4m as at 31 March 2011), trading has been in line with the Board's expectations and we expect full year revenues to 31 March 2012 to be in line with market expectations. During the final quarter of the current year, we expect to trim our R&D expenditure by approximately £1m and now expect R&D costs for the full year to 31 March 2012 to be around £33m. We continue to pay close attention to R&D expenditure to ensure appropriate investment is placed behind key assets, including device and product manufacturing scale up for VR506 and VR315US. Based on our current plans, further reductions in R&D expenditure for FY2013 are also expected. Pipeline update · NVA237 (COPD) § Japanese filing announced in November 2011 § Additional Phase III trial data expected in H1 2012 § EU launch expected in 2012 § US regulatory questions raised in October 2011 to be addressed with further clinical data to be funded by Novartis · QVA149 (COPD) § Phase III trial data expected in H2 2012 § First launch expected in 2013 § US regulatory filing is expected following resolution of questions on NVA237 · Branded generic / generic programmes § Progress continues with VR315 in Europe, US and RoW territories § VR632 progressing towards final development milestone § VR506 clinical programme progressing well Dr Chris Blackwell, Chief Executive of Vectura commented: "We anticipate a number of major catalysts in 2012, including late-stage clinical data from our branded products, the launch of NVA237 in Europe, the EU filing of the combination product, QVA149, as well as progress with our generic programmes. We remain committed to continued cost control, disciplined R&D investment and building Vectura into a sustainably profitable company with strong growth prospects." - Ends - Enquiries
Notes for editors
About Vectura Vectura Group plc develops inhaled therapies principally for the treatment of respiratory diseases. Vectura's main products target diseases such as asthma and chronic obstructive pulmonary disease (COPD), a growing market that is currently estimated to be worth in excess of $25bn.
Vectura has six products marketed by its partners and a portfolio of drugs in clinical and pre-clinical development, a number of which have been licensed to major pharmaceutical companies. Vectura has development collaborations and licence agreements with several pharmaceutical companies, including Novartis, Sandoz (the generics arm of Novartis), Baxter and GlaxoSmithKline (GSK).
Vectura seeks to develop certain programmes itself where this will optimise value. Vectura's formulation and inhalation technologies are available to other pharmaceutical companies on an out-licensing basis where this complements Vectura's business strategy. For further information, please visit Vectura's website at www.vectura.com
Forward-looking statements This press release contains forward-looking statements, including statements about the discovery, development and commercialisation of products. Various risks may cause Vectura's actual results to differ materially from those expressed or implied by the forward-looking statements, including: adverse results in clinical development programmes; failure to obtain patent protection for inventions; commercial limitations imposed by patents owned or controlled by third parties; dependence upon strategic alliance partners to develop and commercialise products and services; difficulties or delays in obtaining regulatory approvals to market products and services resulting from development efforts; the requirement for substantial funding to conduct research and development and to expand commercialisation activities; and product initiatives by competitors. As a result of these factors, prospective investors are cautioned not to rely on any forward-looking statements. We disclaim any intention or obligation to update or revise any forward-looking statements, whether as a result of new information, future events or otherwise.
This information is provided by RNS The company news service from the London Stock Exchange More |
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Found this on another Board, but if you want more rights for the small investors, then sign this petition on the government web site ,everything is private so nobody can find you name and address .And if you want to get our right's back then sign
BE HAPPY REGARDS DAVE http://epetitions.direct.gov.uk/petitions/16769 |
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| 25-01-12 |
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Novartis has today published an innovation update on selected products alongside its annual report. On NVA237 and QVA 149 the update says:
NVA237 (glycopyrronium bromide) is under regulatory review in the EU, where it was submitted for approval in the third quarter of 2011 under the brand name Seebri Breezhaler as a once-daily maintenance treatment for chronic obstructive pulmonary disease. In the fourth quarter, NVA237 was submitted for approval in Japan, where if approved it would be co-promoted with Eisai Co. Ltd. In the US, Novartis is in dialogue with the FDA regarding additional clinical data needed to secure approval. QVA149, a fixed-dose combination of glycopyrronium bromide and indacaterol maleate, remains on track for submission in ex-US countries starting in the fourth quarter of 2012. |
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| 19-01-12 |
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Well at least the Markets seem to have liked it, and the S/P is now moving north once again hopefully back to the £1 mark, but lets hope there is no more un timely news ,such as that from Novartis regarding NVA237 that lead to the over selling off this stock last year . I know the company were not to blame for that RNS, but even so, they could have responded better to it, and cushioned the fall, which should never have happened in the first place, but it did, and it gave some people the chance to top up at a lower price .Any way, its great to see VEC heading north again ,and back to where it should be
GO, VEC ,GO . Be Happy Regards Dave |
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| 19-01-12 |
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Clear presentation by Chris Blackwell (CEO) at the JP Morgan Healthcare conference on 11 January available on the Vectura website - http://www.vectura.com/investors/reports/2012.aspx.
Key points include expectation that NVA237 will be approved and launched in Europe this year; that results from the QVA149 studies will be presented in H2 2012 and launched in first area in 2013. On the generic drugs the CEO sounds confident on the launch of VR315 in Europe without being able to be specific - but he draws attention to the fact their partner Sandoz took up the VR315 rights for the rest of the world. Chris Blackwell explains why VR506 is important to Vectura - aiming at share of $600m market and demonstrating valubale skills. Mention also made of work looking at emerging markets on which announcement expected later. Strong emphasis on determination to reach sustainable profitability. And no bad news. Excellent. |
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