WILEX was founded in September 1997 by a team of
clinical oncologists from the Technical University of Munich led by
Professor Olaf G. Wilhelm. The founders had 15 years of experience
in basis and clinical research on the uPA system and its role in tumour
growth and tumour metastasis. This group was joined in 1999 by Professor
Sven Warnaar of University of Leiden, Netherlands, who served until
his retirement in 2003 as WILEX’s Chief Scientific Officer. In
the early 1990s, Professor Warnaar and his team had discovered the
G250 antibody (today: RENCAREX®) and the G250 (MN/CA IX) antigen
as the therapeutic target of RENCAREX®.
The Company started operations in July 1998 after raising
EUR 3 million in a financing round with a fund advised by Apax Partners
as lead investor.
To-date WILEX has raised EUR 68 million in four private financing rounds
and EUR 55 million through its initial public offering in November
2006.
The funds were used to advance the clinical anti-cancer
product portfolio of the Company and to build up pre-clinical research
projects including academic
collaborations. In particular, the clinical Phase I and Phase II study
programme with the antibody RENCAREX® in renal cell cancer (RCC) were
successfully completed and a Phase III study, which is currently
ongoing, initiated. A
new antibody based diagnostic imaging agent REDECTANE® has been developed.
REDECTANE® is the radioactively labelled form of the antibody WX-G250
and was developed in cooperation with the Ludwig Institute for Cancer
Research, where it demonstrated 100 % positive predictive accuracy
in a feasibility study. In the uPA inhibitor programme, the two drug
candidates WX-UK1
and MESUPRON® were brought from research into clinical development
in cancer patients.
In January 2009 UCB and WILEX entered into strategic
alliance to develop UCB's preclinical oncology portfolio and UCB
became strategic investor of WILEX.
| July 2010 |
dievini Hopp BioTech holding, largest shareholder of
WILEX AG, had to submit a tender offer for a mandatory takeover
bid to all shareholders due to exceeding the 30% limit |
| June 2010 |
WILEX successfully completed Phase I study with the MEK
inhibitor
WX-554 |
| May 2010 |
REDECTANE® meets both endpoints specificity and sensitivity
with superiority over CT in its pivotal Phase III trial |
| May 2010 |
Final Phase II data of MESUPRON® confirm impressive
increase in overall survival of patients with pancreatic cancer |
| October 2009 |
WILEX receives approval for Phase I trial with MEK inhibitor
WX-554 |
| January 2009 |
Strategic alliance with UCB Pharma to develop the preclinical oncological
portfolio of UCB |
| June 2008 |
Licensing agreement with IBA for the worldwide marketing, distribution
and sales of the diagnostic agent REDECTANE® |
| February 2008 |
FDA issues Special Protocol Assessment (SPA) for pivotal Phase III
trial with REDECTANE® |
| December 2007 |
Positive result of the interim analysis for futility of the Phase III ARISER
trial with RENCAREX® |
| November 2006 |
IPO of WILEX AG, Listing at the Regulated Market |
June 2005
|
Fierce Biotech selected WILEX AG as one of the Top 15 emerging Biotech
Companies worldwide |
May 2005
|
Closing of a EUR 30 Mio. series C private equity round |
| October 2004 |
WILEX acquires option for US marketing rights for RENCAREX® from
Centocor |
| April 2004 |
WILEX and Esteve sign co-development and marketing agreement for RENCAREX® in
Southern Europe |
| September 2003 |
WILEX awarded first Biotechnology Clinical Partnership Award from U.S.
Department of Defense Breast Cancer Research Program for the uPA-programme |
November 2002
|
WILEX receives Drug Manufacturing Permission and international GLP
certification from German authorities |
| April 2002 |
WX-G250 receives Orphan Drug Designation in Europe |
| April 2001 |
Transformation of Wilex Biotechnology GmbH in WILEX AG |
| November 2001 |
License agreement with Bayer Corporation for the MN/CA IX antigen for
RENCAREX®/WX-G250
antibody |
| June 2001 |
WX-G250 receives Orphan Drug Designation in USA |
| November 2000 |
Closing of a EUR 30 Mio. series B private equity round |
| August 1999 |
Inlicensing of the G250 antibody (today RENCAREX®) from Centocor |
| April 1999 |
Closing of a EUR 4.5 Mio. series A private equity round |
| July 1998 |
Start of business operation of Wilex Biotechnology GmbH |
| March 1998 |
Closing of a EUR 3 Mio. seedround |
| June 1997 |
Winner of the 1. Munich Businessplan Competition 1996/97 and foundation
of Wilex Biotechnology GmbH |