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Melissa Azallion Appointed Vice-Chair of Lowcountry Workforce Investment Board
HILTON HEAD, SC - Melissa L. Azallion, an employment and immigration attorney in Nexsen Pruet's Hilton Head office, has been appointed vice chair of the Lowcountry Workforce Investment Board.

"Our firm has a tradition of supporting economic opportunity in South Carolina, and workforce development will play a major role in ensuring the state's future prosperity," said Leighton Lord, chairman of the board of Nexsen Pruet. "Melissa’s appointment underscores that tradition and reflects her commitment to community service."

The Workforce Investment Board seeks to work with partners to establish a customer-driven workforce development system that maximizes return on investment and focuses on customer satisfaction.

Board members are nominated by local chambers of commerce/development boards, partner agencies, community-based groups, and other organizations. Members are then appointed by the county councils in Beaufort, Colleton, Hampton, and Jasper.

In her legal practice Azallion represents individuals and corporate clients in multiple industries, including higher education, manufacturing, health care, government, and technology. She is a member of the American Immigration Lawyers Association, the Latin American Council of South Carolina, and the National Association of College and University Attorneys.

Additionally, Azallion is a frequent speaker for business and community organizations on topics such as sexual harassment, immigration, the Americans with Disabilities Act, the Family and Medical Leave Act, Title VII, and wage and hour and workers' compensation issues.

Nexsen Pruet, LLC is one of the largest law firms in the Carolinas, with more than 170 attorneys and offices in Columbia, Charleston, Greenville, Hilton Head, and Myrtle Beach, S.C., and Charlotte and Greensboro, N.C. Founded in 1945, Nexsen Pruet provides a broad range of legal services to the business community and represents companies and other entities in local, state, national, and international venues.

01-09-2006

Davis Graham & Stubbs Hosting Annual Corporate Update
Denver, Colorado - Davis Graham & Stubbs' corporate attorneys are presenting
their annual securities law breakfast briefing on Thursday, January 26, from 7:30 to 10:00
a.m. at their LoDo offices. The "2006 Public Company Update" is designed for executives,
including CEOs, CFOs, in-house lawyers, accountants, investment bankers, investor relations
professionals and others, involved in corporate compliance with securities laws. Some of the
topics scheduled for coverage include:
- how the securities offering reforms will affect the ability to raise capital;
- what has happened to the legal environment for fundamental corporate
transactions; and
- how changes in the proxy process and annual meeting will affect business.
Two CLE and/or CPE credits have been approved for this seminar. For more information, or to
reserve a seat at this complimentary briefing, please contact Nancy Meyer at (303) 892-7584.Davis Graham & Stubbs is a leading law firm in the Rocky Mountain region,with approximately 100
lawyers focused on three major practice areas: Finance & Acquisitions,Natural Resources and Trial.
For more information about the firm, its practices, and its lawyers, please visit www.dgslaw.com.

01-09-2006

WELL-KNOWN ATTORNEY JOINS FIRM’S EXPANDING LITIGATION PRACTICE
Laura J. Gerdes joins local law firm Danna McKitrick, P.C. as their
newest litigation associate. Gerdes is an experienced attorney focusing on tort, employment, insurance,
municipal and healthcare law. She also consults and trains on employment law policies and processes,
especially related to the privacy and security requirements under the Health Insurance Portability and
Accountability Act of 1996 (HIPAA).
Gerdes speaks on HIPAA and its effect on municipalities, fire protection districts, emergency medical
services, physicians and employers. For over two years, she served as an independent contract lawyer
for the City of St. Louis on HIPAA compliance issues. She previously served as prosecutor for Velda City,
Bella Villa, and Normandy, and as assistant city attorney for various other municipalities throughout St.
Louis County.
“We are very pleased to welcome Laura to our practice,” says Dan Tobben, a key principal in the
firm’s litigation department. “Both Dale Weppner and I have worked with Laura in the past and we
know her skills to be sharp and her judgment excellent. It is great to have another strong,
analytical thinker on our team.”
Gerdes earned her J.D. from Washington University School of Law and her B.A., cum laude, in European
Studies with a focus on Russia from Vanderbilt University.
Located in Clayton, Missouri, Danna McKitrick, P.C. is a 24 attorney firm delivering outstanding
legal representation to businesses, insurers, and individuals in the Midwestern region. The firm has
long-standing local roots serving many local businesses as well as regional representation for
insurance companies and major corporations. The firm is on the Web at www.dannamckitrick.com.

01-09-2006

ST LOUIS LAWYER/CPA JOINS FIRM’S TRANSACTION TEAM
Local law firm Danna McKitrick, P.C. is pleased to welcome lawyer
and CPA, Patrick J. Murphy, to the practice. With a strong background in private legal practice and past
experience in public accounting—including Ernst & Young—Murphy serves small to medium-sized
businesses and their owners working on mergers and acquisitions, real estate transactions and personal
estate and trust planning.
“We’re so glad to have Patrick here,” says Cheryl Beebe-Snell, a key principal in business and
tax law. “His easy way with people and excellent technical background are just the right mix for
our firm’s clients.”
Murphy earned his J.D. from Saint Louis University School of Law and his B.S.B.A. in Accounting from
Creighton University. He is a native of the Metro East and currently resides in Brentwood.
Located in Clayton, Missouri, Danna McKitrick, P.C. is a 24 attorney firm delivering outstanding
legal representation to businesses, insurers, and individuals in the Midwestern region. The firm has
long-standing local roots serving many local businesses as well as regional representation for
major corporations. The firm is on the Web at www.dannamckitrick.com.

01-09-2006

(Livonia, MI)- The law firm of Cummings, McClorey, Davis & Acho is pleased to announce that three attorneys recently joined the firm
Derek J. Brackon joined the firm as an associate. He is working out of both their Roseville and Livonia office. His practice areas include family law (divorce, custody and support issues), municipal liability defense and general commercial litigation. He is a member of the Macomb County Bar Association, State Bar of Michigan and American Bar Association.
Mr. Brackon received a Juris Doctor degree from Wayne State University Law School (2000) and a Bachelor of Arts degree in Economics from the University of Michigan (1997).
Nellie J. Lim joined their Livonia office as an associate. Her practice areas include municipal law, insurance defense, personal injury litigation and commercial litigation. She is a member of the State Bar of Michigan, American Bar Association and the Asian American Bar Association. Ms. Lim received a Juris Doctor degree from Wayne State University Law School (2002) and a Bachelor of Arts degree, cum laude, in Psychology from Wayne State University (1999).
Gary L. Hudson, Jr. joined their Grand Rapids office as an associate. His practice areas include insurance defense, construction defect, personal injury, product liability defense, first and third party bad faith claims and insurance coverage analysis. He is admitted to practice law in both Michigan and Arizona.
Mr. Hudson received a Juris Doctor degree, cum laude, from the University of Toledo (1996) and a Bachelor of Arts degree, magna cum laude, in Political Science from Kent State University (1993).
Cummings, McClorey, Davis & Acho is a full-service law firm offering experienced practioners in all federal, state and administrative courts. The firm has an extensive practice in governmental law, employment and labor law, insurance coverage, personal injury defense and litigation, corporate and business law and appellate practice.

01-09-2006

Department Of Justice Attorney And Former Enron Task Force Member Thomas Hanusik Joins Crowell & Moring's Growing White Collar & Securities Litigation Group
Thomas A. Hanusik, an Assistant Chief of the Department of Justice's Criminal Division, Fraud Section, has joined Crowell & Moring LLP's White Collar & Securities Litigation Group as partner. Hanusik, a former member of the Justice Department's Enron Task Force and a former Senior Counsel for the Securities and Exchange Commission's Division of Enforcement, is the fourth new hire to join the firm's growing White Collar & Securities Litigation Group in the last month.
Hanusik's 12 years of experience at the Justice Department and SEC strengthens both the firm's white collar defense and securities litigation practices. In December, the group hired Philip T. Inglima, the former Senior Associate Independent Counsel in the investigation of Department of the Interior Secretary Bruce Babbitt, along with two other former Justice Department attorneys.
“We offer a premier White Collar & Securities Litigation Group that boasts first-hand experience in the highest profile matters facing the business world in recent years. The addition of Tom is an important part of our strategy to recruit the very best in this field,” said Crowell & Moring chairman John A. Macleod.
Throughout his career at both the Justice Department and the SEC, Hanusik led, supervised and coordinated a number of parallel criminal grand jury and civil law enforcement investigations. In addition to securities and commodities fraud work, Hanusik has investigated and prosecuted criminal and civil cases involving the Foreign Corrupt Practices Act, conspiracy, bank fraud, insider trading, money laundering, counterfeiting, identity theft, social security fraud and education loan fraud.
Hanusik was one of the original six prosecutors on the Enron Task Force, where he worked with the SEC and agents from the FBI and Internal Revenue Service to investigate Enron's collapse. Hanusik's other work has included the prosecution of executives with Enterasys Network Systems, Inc. and, during 2005, he led the Justice Department's prosecution team investigating the abuse of finite reinsurance products and prosecuted a number of high-ranking insurance executives. Hanusik is a graduate of Fordham College and Duke Law School.
For more than twenty years, Crowell & Moring's White Collar & Securities Litigation Group has defended clients from across the country and around the world with interests affected by investigations in federal judicial districts throughout the United States. The practice spans investigations by grand juries, congressional committees, independent and special counsels, federal agency inspectors general, and other investigative officials and bodies.
Crowell & Moring LLP is a full-service law firm with more than 300 attorneys practicing in litigation, antitrust, government contracts, corporate, intellectual property and more than 40 other practice areas. More than two-thirds of the firm's attorneys regularly litigate disputes on behalf of domestic and international corporations, start-up businesses, and individuals. Crowell & Moring's extensive client work ranges from advising on one of the world's largest telecommunications mergers to representing governments and corporations on international arbitration matters. Based in Washington, D.C., the firm also has offices in Brussels, California and London.

01-09-2006

CancerVax and Micromet Announce Merger Agreement
Carlsbad, CA and Munich, GERMANY (MARKET WIRE), 01/09/2006 -- CancerVax Corporation (NASDAQ: CNVX), a biotechnology company focused on the research, development and commercialization of novel biological products for the treatment of cancer, and Micromet AG, one of the leading privately held European biopharmaceutical companies focused on the development of antibody-based drugs, announced today the signing of a definitive merger agreement. The merger is expected to create a transatlantic, NASDAQ-listed company with a highly differentiated drug development pipeline focused on oncology, autoimmune and inflammatory diseases, and a strong, proprietary technology base for the development of antibody-based product candidates.
"We believe that the proposed merger of CancerVax and Micromet is consistent with our objective of maximizing value for our stockholders, and will result in an organization with a robust pipeline of drug candidates as well as significant experience in drug discovery and development," said David F. Hale, President and CEO of CancerVax Corporation.
"This transaction will allow Micromet to access U.S. capital markets, which is essential in our efforts to accelerate the development of our novel, antibody-based drug compounds based on our proprietary BiTE™, or bi-specific T cell engager, and single-chain antibody drug development platforms," said Christian Itin, Ph.D., CEO of Micromet. "It also strengthens our management team and financial position, allows us to leverage CancerVax's existing U.S. public company infrastructure, and adds to our product development portfolio."
The merged company will have a substantial product pipeline, with two compounds in clinical development in three major cancer indications and several preclinical and research-stage product candidates.
Product Candidate, Indication, Development Stage, Collaboration
MT201,Adecatumumab (human antibody), Metastatic Breast Cancer & Prostate Cancer, Phase 2, Serono
MT103 (BiTE™), Non-Hodgkin's Lymphoma (NHL), Phase 1, MedImmune, Inc.
MT110 (BiTE™), Solid Tumors, Pre-clinical, ---
MT203 (human antibody), Inflammatory Diseases, Pre-clinical, ---
D93 (humanized antibody), Solid Tumors, Pre-clinical,---
Details of the Proposed Transaction
Under the terms of the merger agreement, CancerVax will issue, and Micromet stockholders will receive, shares of CancerVax stock such that Micromet stockholders will own approximately 67.5 percent of the combined company, on a pro forma basis, and CancerVax stockholders will own approximately 32.5 percent. It is anticipated that, on a pro forma basis, cash, cash equivalents and securities available-for-sale for the combined Companies as of December 31, 2005 will be between $57 million and $60 million. The merger is intended to qualify for federal income tax purposes as a tax-free reorganization under the provisions of Section 368(a) of the U.S. Internal Revenue Code of 1986, as amended. The merger agreement has been approved by both Boards of Directors and will need to be approved by each company's stockholders.
CancerVax expects to file a Form S-4 and related proxy statement/prospectus with the U.S. Securities and Exchange Commission and any other necessary government filings in the coming weeks. Depending on the review process of the agencies, the Companies would expect their respective stockholder votes to occur in the second quarter of 2006. Upon closing of the transaction, the Company's shares are expected to continue to trade on the NASDAQ National Market. CancerVax will be renamed as Micromet, Inc., and application will be made to NASDAQ to change the ticker symbol to "MITI." Piper Jaffray & Co. served as financial advisor and Latham and Watkins LLP as legal advisor to CancerVax. Cooley Godward LLP served as legal advisor to Micromet.
Management and Organization
Following the closing, the merged Company's U.S. headquarters will be in Carlsbad, CA, while the Company's German headquarters will remain in Munich, Germany. Research and development activities will be consolidated in Munich.
David F. Hale, currently President and Chief Executive Officer of CancerVax, will become Chairman of the Board of Directors of the merged company. Micromet's Chief Executive Officer, Christian Itin, will become President and CEO and serve on the Board of Directors. Patrick Baeuerle, currently Chief Scientific Officer of Micromet, will become CSO of the combined entity. CancerVax's Chief Financial Officer, William R. LaRue, will serve as CFO of the merged company. Gregor Mirow, Micromet's Chief Financial and Chief Operating Officer, will be COO, and Hazel M. Aker, CancerVax's General Counsel, will continue to serve as General Counsel. The combined company's Board of Directors will consist of five current Micromet directors, including one director who is also currently a director of CancerVax, three other CancerVax directors and a ninth director to be named by Micromet prior to the merger.
Outlook for 2006
Following the merger, the Company plans to focus its resources on accelerating the development of its clinical-stage product development programs and leveraging its strong R&D base and pipeline-generating capabilities related to human antibodies, BiTE™ molecules and single-chain antibodies. The Company also plans to continue to build on Micromet's track record of successfully establishing drug development collaborations with major pharmaceutical companies, while retaining substantial commercial rights.
Anticipated milestones for the merged Company in 2006 include:
Closing the merger transaction in the second quarter;
Phase 2 clinical trial results for MT201 in patients with metastatic breast cancer and in patients with prostate cancer;
Phase 1 results for MT103 in the treatment of patients with NHL;
Filing of an investigational new drug application in the first quarter to initiate clinical trials with D93; and
Continuing to pursue partnering opportunities.
MT201 - Adecatumumab
Micromet's lead product candidate, MT201, is a recombinant human monoclonal antibody of the IgG1 subclass with a binding specificity to epithelial cell adhesion molecule (Ep-CAM). Ep-CAM is over-expressed with high frequency on most solid tumor types, including prostate, breast, colon, gastric, ovarian and lung cancer. MT201 is in Phase 2 clinical trials in patients with prostate cancer and metastatic breast cancer. In addition, MT201 is being evaluated as a combination therapy with Taxotere® (docetaxel) in a Phase I clinical trial in patients with metastatic breast cancer. The FDA has approved an investigational new drug application for MT201 for the treatment of patients with metastatic breast cancer.
In December 2004, Micromet announced an exclusive worldwide collaboration and license agreement with Serono, a Swiss corporation, for the development and commercialization of MT201. Micromet received an initial license fee of US$10 million and may receive additional milestone payments of up to US$138 million if the product is successfully developed and registered worldwide in three or more indications. In addition, Micromet may receive undisclosed royalties based on net sales of the product. Under certain terms and conditions, Micromet may elect to share in the development and commercialization of the product in the U.S. and E.U. in exchange for a share of profits.
MT103
Micromet's other leading product candidate, MT103, is being studied in a European Phase 1 clinical trial. MT103 represents a new class of therapeutics that may be capable of instructing the patients' own T cells (a very potent type of killer cell) to repeatedly eliminate tumor cells. This technology is called BiTE™ (bi-specific T cell engager). MT103 binds to CD19 on B cells, a cell surface antigen.
In June 2003, Micromet announced an agreement to jointly develop MT103 with MedImmune, Inc. Under the terms of the agreement, Micromet would receive milestone payments based on the successful development, filing, registration and marketing of MT103, as well as royalties on MedImmune's North American sales of the product. Micromet retained all rights to the product candidate outside of North America.
D93
CancerVax's D93 is a humanized, monoclonal antibody being studied for the treatment of solid tumors, which has been shown to selectively bind to denatured or remodeled protein in diseased or damaged tissues, but not to native collagen in the extra-cellular matrix of healthy tissue. D93 has demonstrated the ability to selectively bind to denatured collagen targets in colon, melanoma, lung, and breast cancer tumors grown in xenogeneic mouse models. The Company expects to submit an investigational new drug application for D93 to the FDA in the first quarter of 2006, and plans to initiate the first clinical trial for D93 later in 2006.
Micromet's BiTE™ Technology
Micromet's BiTE™ technology represents a novel therapeutic modality with the potential to develop antibody-based products to improve the treatment of diseases that currently lack satisfactory treatment options and that are resistant or refractory to standard therapies. BiTE™ molecules constitute a novel class of bi-specific antibodies that appear to be unique in their ability to activate the body's killer T cells against target cells. The proposed mechanism of action of Micromet's BiTE™ technology involves the activation of the available T cells in a patient's body, regardless of their specificity. This approach may have advantages, since in cancer therapy, patient-derived cancer tissue has to be recognized as "foreign" and eliminated by the patient's T cells. In many cases, tumors evade the recognition mechanisms used by T cells, in particular, and thus cannot be controlled by the patient's immune system. In summary, BiTE™ molecules are designed to provide each T cell with the ability to circumvent a number of tumor cell defense mechanisms.
Single-Chain Antibodies
Single-chain antibodies, which are used in the construction of BiTE™ product candidates, have demonstrated potential as therapeutics, diagnostics and as research tools. Single-chain antibodies comprise the antigen-binding site of antibodies engineered as a single protein. Under an agreement with Enzon Pharmaceuticals, Inc. Micromet is the exclusive licensor of the two companies' combined intellectual property estate in the field of single-chain antibody technology. Current licensees include Alexion Pharmaceuticals, Alligator Bioscience, Amersham Pharmacia, Arizeke Pharmaceuticals, Baxter Healthcare Corporation, BioInvent International AB, Bristol-Myers Squibb Company, Cambridge Antibody Technology, UCB Pharma, Crucell, EvoGenix, ESBATech, Invitrogen, MorphoSys, Merck & Co., Neoprobe Corporation and Xoma Corporation.
Conference Call Monday, January 9, at 9:00 AM Eastern Time / 03:00 PM Central European Time
CancerVax and Micromet will host a joint conference call on Monday, January 9, to discuss the planned merger and its business overview at 9:00 a.m. Eastern Time. A live audio webcast of management's presentation will be available at http://ir.cancervax.com. Alternatively, callers may participate in the conference call by dialing (866) 700-7173 (domestic) or (617) 213-8838 (international). The passcode for the call is 36272047. Following the call, the webcast will be archived on the investor relations section of the CancerVax website.
About CancerVax Corporation (www.cancervax.com)
CancerVax Corporation is a biotechnology company focused on the research, development and commercialization of novel biological products for the treatment and control of cancer. The Company's leading product candidate is D93, an anti-angiogenic, humanized, monoclonal antibody. CancerVax plans to file an investigational new drug application for clinical trials of D93 in the first quarter of 2006. Upon the consummation of the merger, the Company intends to focus on the development of antibody-based product candidates for the treatment of cancer and inflammatory and autoimmune diseases. As a result, CancerVax is actively seeking to sublicense its rights to its three licensed product candidates that target the epidermal growth factor receptor signalling pathway.
About Micromet (www.micromet.de)
Micromet AG is a private Munich, Germany-based biotechnology company with a focus on the development of novel, proprietary antibody-based products for cancer and inflammatory and autoimmune diseases. Two product candidates are currently in clinical trials. MT201, a recombinant human monoclonal antibody is being evaluated in Phase 2 clinical trials for the treatment of certain solid tumors. MT103 is being studied in a Phase 1 clinical trial. The Company has established a powerful drug development platform based on its BiTE™ technology, a unique drug format that leverages the cytotoxic potential of T cells, the most powerful 'killer cells' of the human immune system. Micromet has integrated infrastructure and expertise in all disciplines of drug design and development. The Company has attracted both top-tier life science investors and collaborators, such as MedImmune, Inc. and Serono.
Forward-Looking Statements
This release contains certain forward-looking statements that involve risks and uncertainties that could cause actual results to be materially different from historical results or from any future results expressed or implied by such forward-looking statements. Such forward-looking statements include statements regarding the proposed transaction, the efficacy, safety, and intended utilization of the companies' respective product candidates, the conduct and results of future clinical trials, and plans regarding regulatory filings, future research and clinical trials and plans regarding partnering activities. Factors that may cause actual results to differ materially include the risk that CancerVax and Micromet may not be able to complete the proposed transaction, the risk that product candidates that appeared promising in early research and clinical trials do not demonstrate safety and/or efficacy in larger-scale or later clinical trials, the risk that CancerVax and Micromet will not obtain approval to market their respective products, the risks associated with reliance on outside financing to meet capital requirements, and the risks associated with reliance on collaborative partners for further clinical trials, development and commercialization of product candidates. You are urged to consider statements that include the words "may," "will," "would," "could," "should," "believes," "estimates," "projects," "potential," "expects," "plans," "anticipates," "intends," "continues," "forecast," "designed," "goal," or the negative of those words or other comparable words to be uncertain and forward-looking. The transaction is subject to customary closing conditions, including approval of CancerVax's and Micromet's stockholders. These factors and others are more fully discussed in CancerVax's periodic reports and other filings with the SEC.
Any forward-looking statements are made pursuant to Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended, and, as such, speak only as of the date made. CancerVax undertakes no obligation to publicly update any forward-looking statements, whether as a result of new information, future events or otherwise.
Additional Information about the Merger and Where to Find It
In connection with the proposed transaction described herein, CancerVax will file a registration statement that contains a proxy statement/prospectus with the SEC. Investors and security holders of CancerVax and Micromet are urged to read the proxy statement/prospectus (including any amendments or supplements to the proxy statement/prospectus) regarding the proposed transaction when it becomes available because it will contain important information about CancerVax, Micromet and the proposed transaction. CancerVax's stockholders will be able to obtain a copy of the proxy statement/prospectus, as well as other filings containing information about CancerVax and Micromet, without charge, at the SEC's Internet site (http://www.sec.gov). Copies of the proxy statement/prospectus and the filings with the SEC that will be incorporated by reference in the proxy statement/prospectus can also be obtained, without charge, by directing a request to CancerVax Corporation, 2110 Rutherford Road, Carlsbad, CA 92008, Attention: Investor Relations, Telephone: (760) 494-4200.
Participants in the Solicitation
CancerVax and its directors and executive officers and Micromet and its directors and executive officers may be deemed to be participants in the solicitation of proxies from the stockholders of CancerVax in connection with the proposed transaction. Information regarding the special interests of these directors and executive officers in the merger transaction will be included in the proxy statement/prospectus referred to above. Additional information regarding the directors and executive officers of CancerVax is also included in CancerVax's proxy statement for its 2005 Annual Meeting of Stockholders, which was filed with the SEC on April 28, 2005. This document is available free of charge at the SEC's web site (www.sec.gov) and from Investor Relations at CancerVax at the address described above.

01-09-2006

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