Telephone conference for analysts and the media via webcast today, November 10, 2016, 3 pm CET (Munich/Frankfurt) / 9:00 am EST (New York)
Martinsried, Munich, November 10, 2016. Medigene AG (MDG1, Frankfurt, Prime Standard), a clinical stage immuno-oncology company focusing on the development of T-cell immunotherapies for the treatment of cancer, today reports financial results and corporate updates for the first nine months of 2016.
Major events since the beginning of 2016
Key figures in the first nine months of 2016:
Prof. Dolores Schendel, CEO and CSO of Medigene AG comments, "The first nine months of 2016 were very successful and topped by the collaboration agreement with bluebird bio. Having our TCR technology validated by such a top tier biotechnology company at this early stage of development is a huge success for Medigene and we are delighted that we can continue to grow on the basis of our scientific and commercial development. In addition to the ongoing generation of new own TCRs and independent of the bluebird bio alliance, we plan to recruit new staff to expand the TCR technology platform. We will implement new tools and technologies to place the TCR technology platform on a broader base and to expand its applicability. We are on schedule with our preparations for the planned clinical TCR trials and our ongoing Phase I/II trial for DC vaccines."
Dave Lemus, Chief Operating Officer of Medigene AG adds, "We are very satisfied with the operational business of our core business to date. Medigene's collaboration with bluebird bio, a recognized leader in cell-therapies, is a clear validation of our TCR technology and affirms the significant potential of this technology. Moreover, our collaboration with bluebird bio provides us with a further strengthened financial foundation from which we can invest additional resources into our own proprietary products, technologies and people."
|In € k||
|Results of operations|
|thereof Veregen ® revenue||2,208||2,376||-7%|
|thereof other operating income||4,844||2,950||64%|
|thereof gain on sale of intangible assets, net (EndoTAG)||2,365||0||-|
|Cost of sales||-1,127||-862||31%|
|Selling and general administrative expenses||-7,645||-5,517||39%|
|Research and development expenses||-7,985||-6,214||29%|
|Income from the sale of financial assets||4,242||0||-|
|Net profit/loss for the period||-5,725||-10,554||-46%|
|Earnings per share (€)||-0.29||-0.67||-57%|
|Net cash used in operating activities||-12,992||-7,642||70%|
|Net cash from/used in investing activities||10,013||-420||>-200%|
|Net cash from/used in financing activities||-181||43,855||-100%|
|Balance sheet data as at Sep 30, 2016 and Dec 31, 2015|
|Cash and cash equivalents and time deposits||43,599||46,759||-7%|
|Equity ratio (%)||71||79||-10%|
|Employees as at 30 September||84||71||18%|
|FTE as at 30 September||77||65||18%|
|Medigene share as at 30 September|
|Total number of shares outstanding||20,136,887||19,678,221||2%|
|Share price (XETRA closing price) (€)||8.19||6.14||33%|
Financial guidance 2016:
The Company confirms its financial guidance for 2016 published in the 2015 annual report. Due to the expansion of its clinical development programs, Medigene is planning to significantly increase R&D expenses in the field of immunotherapies to between € 9 - 11m (2015: € 5.5m) in 2016. The EBITDA loss for 2016 is expected to lie between € 10 -12m (2015: € 9.5m).
The Company expects total Veregen ® revenue of € 3 - 4m (2015: € 3.1m), and stable or increasing total revenue for 2016 (2015: € 6.8m). Since this revenue is not generated in the Company's core business, these figures are not conclusive with regard to the Company's core business, i.e. immunotherapies. This financial guidance assumes constant foreign exchange rates.
Outlook for immunotherapies:
TCR-modified T cells (TCRs):
Medigene aims to initiate up to three clinical trials for this therapy, the first to be started in 2017. This publicly sponsored investigator-initiated Phase I trial with participation from Medigene is the first clinical TCR trial in Germany. Medigene-sponsored trials are planned to start in the second half of 2017 and in the second half of 2018. A GMP-compliant manufacturing process for TCRs is being developed in advance of Medigene's TCR trials. In addition, novel TCRs with specificities for promising tumor-associated antigens will be isolated and further characterized.
In addition to the ongoing generation of new own T cell receptors (TCRs), Medigene plans to recruit new staff to expand the TCR technology platform. The Company intends to implement new tools and technologies to place the TCR technology platform on a broader base and to expand its applicability. A part of Medigene's TCR team will be dedicated to the partnershiprecently announced with the US company, bluebird bio. The costs of the personnel working within the framework of this cooperation agreement and the research and development expenses will be fully absorbed by bluebird bio. Medigene will assign the remaining capacity of the expanded TCR team to broaden its own TCR program efforts.
DC vaccines (DCs):
Medigene will continue the current Phase I/II clinical trial for the treatment of acute myeloid leukemia (AML) and, on the back of positive safety data as well as on data from the University Oslo from compassionate uses, will extend the vaccination of the patients until the scheduled completion of the trial (a two-year treatment) with the overall duration of the trial remaining at two years per patient. The former treatment period was one year followed by a one-year observation period. This has now been replaced by a longer treatment period under the adjusted design of the trial. Medigene anticipates additional positive effects for the patients being treated with no change to the safety profile or duration of the overall trial. The final data from the clinical trial will be published in the second half of 2019, as scheduled.
The complete Q3 2016 report is available at http://www.medigene.com/media-investors/reports-presentations/financial-reports
Analyst and press conference: A telephone conference (webcast) in English will be held today at 3:00 pm CET (Munich/Frankfurt) / 9:00 am EST (New York) and transmitted live in the internet. Access and transmission of the synchronized presentation slides and a recording of the presentation is available on the homepage of Medigene at www.medigene.com .
Medigene AG is a publicly listed (Frankfurt: MDG1, prime standard) biotechnology company headquartered in Martinsried near Munich, Germany. The Company develops highly innovative, complementary treatment platforms to target various forms and stages of cancer with drug candidates in clinical and pre-clinical development. Medigene concentrates on the development of personalized T-cell-based immunotherapies.
More information is available at www.medigene.de
This press release contains certain statements relating to the future. They represent the opinion of Medigene as of the date of this release. The actual results achieved by Medigene may differ significantly from the forward-looking statements made herein. Medigene is not bound to update any of these forward-looking statements Medigene ® and Veregen® are registered trademarks of Medigene AG. EndoTAG ® is a registered trademark of SynCore Biotechnology Co., Ltd. These trademarks may be held or licensed for specific countries.
Julia Hofmann, Dr. Robert Mayer
Tel.: +49 - 89 - 20 00 33 - 33 01
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Last updated on: 11/11/2016
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