Genmab Launches Sponsored Level 1 American Depositary Receipt (ADR) Program
31 Maio 2013 - 10:19AM
Company Announcement
- Genmab establishes Sponsored Level 1 ADR
program
- Genmab ADRs can be traded on US over-the-counter (OTC)
market effective today
- ADR ticker symbol GMXAY
COPENHAGEN, Denmark, May 31, 2013 (GLOBE NEWSWIRE) --
Genmab A/S (Copenhagen:GEN) announced
today the establishment of a Sponsored Level 1 ADR program in the
United States. Deutsche Bank Trust Company Americas will
act as the depositary bank for the Genmab ADR program.
Genmab ADRs are US dollar negotiable certificates representing
ordinary Genmab shares; two Genmab ADRs represent one Genmab share.
Genmab ADRs can be traded on the US over-the-counter (OTC) market
effective May 31, 2013 under the ticker symbol GMXAY. Ordinary
Genmab shares are traded on the NASDAQ OMX Copenhagen A/S under the
ticker symbol GEN.
"We have established an ADR program for Genmab as a service to
offer US investors an alternative way to buy Genmab shares.
We hope this effort will serve to broaden Genmab's international
shareholder base and increase general interest in the company,"
said Jan van de Winkel, Ph.D., Chief Executive Officer of
Genmab.
About ADRs
An ADR program allows US investors to more easily purchase, hold
or sell non-US securities. ADRs represent ordinary shares of a
company which are traded on a foreign (non-US) stock exchange. In a
Sponsored Level 1 ADR program, a US investment broker can purchase
or sell a company's ordinary shares on the market; the purchased
shares are deposited with a depositary bank. In exchange, the
depositary bank issues ADR shares which are traded in US dollars on
the OTC market.
About Genmab A/S
Genmab is a publicly traded, international biotechnology company
specializing in the creation and development of differentiated
human antibody therapeutics for the treatment of cancer.
Founded in 1999, the company's first marketed antibody,
ofatumumab (Arzerra(r)), was approved to treat chronic lymphocytic
leukemia in patients who are refractory to fludarabine and
alemtuzumab after less than eight years in development.
Genmab's validated and next generation antibody technologies
are expected to provide a steady stream of future product
candidates. Partnering of innovative product candidates and
technologies is a key focus of Genmab's strategy and the company
has alliances with top tier pharmaceutical and biotechnology
companies. For more information visit www.genmab.com.
Contact:
Rachel Curtis Gravesen, Senior Vice President, Investor Relations
& Communications T: +45 33 44 77 20; M: +45 25 12 62 60; E:
r.gravesen@genmab.com
This Company Announcement contains forward looking statements.
The words "believe", "expect", "anticipate", "intend" and "plan"
and similar expressions identify forward looking statements. Actual
results or performance may differ materially from any future
results or performance expressed or implied by such statements. The
important factors that could cause our actual results or
performance to differ materially include, among others, risks
associated with pre-clinical and clinical development of products,
uncertainties related to the outcome and conduct of clinical trials
including unforeseen safety issues, uncertainties related to
product manufacturing, the lack of market acceptance of our
products, our inability to manage growth, the competitive
environment in relation to our business area and markets, our
inability to attract and retain suitably qualified personnel, the
unenforceability or lack of protection of our patents and
proprietary rights, our relationships with affiliated entities,
changes and developments in technology which may render our
products obsolete, and other factors. For a further discussion of
these risks, please refer to the risk management sections in
Genmab's most recent financial reports, which are available on
www.genmab.com . Genmab does not undertake any obligation to update
or revise forward looking statements in this Company Announcement
nor to confirm such statements in relation to actual results,
unless required by law.
Genmab A/S and its subsidiaries own the following trademarks:
Genmab(r); the Y-shaped Genmab logo(r); HuMax(r); HuMax-CD20(r);
DuoBody(r), HexaBodyTM and UniBody(r). Arzerra(r) is a trademark of
GlaxoSmithKline.
Company Announcement no. 25 CVR no. 2102 3884
Genmab A/S Bredgade 34E 1260 Copenhagen K Denmark