-----BEGIN PRIVACY-ENHANCED MESSAGE----- Proc-Type: 2001,MIC-CLEAR Originator-Name: webmaster@www.sec.gov Originator-Key-Asymmetric: MFgwCgYEVQgBAQICAf8DSgAwRwJAW2sNKK9AVtBzYZmr6aGjlWyK3XmZv3dTINen TWSM7vrzLADbmYQaionwg5sDW3P6oaM5D3tdezXMm7z1T+B+twIDAQAB MIC-Info: RSA-MD5,RSA, RWuYs9N4a+6RFSnW55I6ajYvcKpEgjYU/C2/VMJOdt1+HhsdE1q5Drnzio9WOkYh pe5Qs2yat9Q3Bwqf9RO5Nw== 0000912057-02-016575.txt : 20020425 0000912057-02-016575.hdr.sgml : 20020425 ACCESSION NUMBER: 0000912057-02-016575 CONFORMED SUBMISSION TYPE: 8-K PUBLIC DOCUMENT COUNT: 2 CONFORMED PERIOD OF REPORT: 20020424 ITEM INFORMATION: Other events ITEM INFORMATION: Financial statements and exhibits FILED AS OF DATE: 20020425 FILER: COMPANY DATA: COMPANY CONFORMED NAME: VALENTIS INC CENTRAL INDEX KEY: 0000932352 STANDARD INDUSTRIAL CLASSIFICATION: BIOLOGICAL PRODUCTS (NO DIAGNOSTIC SUBSTANCES) [2836] IRS NUMBER: 943156660 STATE OF INCORPORATION: DE FISCAL YEAR END: 0630 FILING VALUES: FORM TYPE: 8-K SEC ACT: 1934 Act SEC FILE NUMBER: 000-22987 FILM NUMBER: 02621040 BUSINESS ADDRESS: STREET 1: 863A MITTEN RD CITY: BURLINGAME STATE: CA ZIP: 94010 BUSINESS PHONE: 6506971900 MAIL ADDRESS: STREET 1: 863A MITTEN ROAD CITY: BURLINGAME STATE: CA ZIP: 94010 FORMER COMPANY: FORMER CONFORMED NAME: MEGABIOS CORP DATE OF NAME CHANGE: 19960716 8-K 1 a2077842z8-k.htm 8-K
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SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549


Form 8-K

CURRENT REPORT

Pursuant to Section 13 or 15(d) of the
Securities Exchange Act of 1934

April 24, 2002
Date of report (Date of earliest event reported)

Valentis, Inc.
(Exact name of registrant as specified in its charter)

Delaware   0-22987   94-3156660
(State of Incorporation)   (Commission File Number)   (IRS Employer Identification No.)

863A Mitten Road, Burlingame, California 94010
(Address of principal executive offices) (Zip Code)

(650) 697-1900
(Registrant's telephone number, including area code)





Item 5. Other Events.

        On April 24, 2002, Valentis, Inc. (the "Company") announced that its wholly-owned subsidiary, PolyMASC Pharmaceuticals Plc (PolyMASC), has been granted European Patent Number EP572,049B1, covering PEGylated liposomes (liposomes having polyethylene glycol (PEG) chains attached). In addition, the Company announced that PolyMASC has initiated infringement proceedings in Germany, against SP Labo N.V., SP Europe and Essex Pharma GmbH, all members of the Schering Plough Group. The suit alleges infringement of this patent and patent EP445,131B1, also owned by PolyMASC, based on the sales of Caelyx®, a PEGylated-liposome product encapsulating the drug doxorubicin. Finally, the Company has announced the end of its alliance with Roche Holdings Ltd. with respect to the development of intratumoral cancer immunotherapy products. A copy of the Company's press release regarding this announcement is set forth in Exhibit 99.1 attached hereto and incorporated by reference.


Item 7. Financial Statements, Pro Forma Financial Information and Exhibits.

    (c)
    Exhibits.

  99.1   Text of Press Release, dated April 24, 2002.

2



SIGNATURE

        Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.

Dated: April 25, 2002

    VALENTIS, INC.

 

 

By:

 

/s/  
BENJAMIN F. MCGRAW III      
Benjamin F. McGraw III, Pharm. D.
President and Chief Executive Officer

3



EXHIBIT INDEX

Exhibit Number
  Description

99.1   Text of Press Release, dated April 24, 2002.



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SIGNATURE
EXHIBIT INDEX
EX-99.1 3 a2077842zex-99_1.htm EXHIBIT 99.1
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Exhibit 99.1


VALENTIS ANNOUNCES ISSUANCE OF PEGYLATED LIPOSOMES
PATENT IN EUROPE, INITIATION OF INFRINGEMENT SUIT, AND
ONCOLOGY PROGRAM UPDATE

        Burlingame, Calif., April 24, 2002—Valentis, Inc. (NASDAQ:VLTS) announced that its wholly-owned subsidiary, PolyMASC Pharmaceuticals Plc, has been granted European Patent Number EP572,049B1, covering PEGylated liposomes (liposomes having polyethylene glycol (PEG) chains attached). In addition, Valentis announced that PolyMASC has initiated infringement proceedings in Germany, against SP Labo N.V., SP Europe and Essex Pharma GmbH, all members of the Schering Plough Group. The suit alleges infringement of this patent and patent EP445,131B1, also owned by PolyMASC, based on the sales of Caelyx®, a PEGylated-liposome product encapsulating the drug doxorubicin.

        Patent EP572,049B1, titled "Liposomes," is the European counterpart to U.S. Patent Number 6,132,763. PolyMASC initiated infringement proceedings against ALZA Corporation in the United States in April 2001, for infringement of U.S. Patent Number 6,132,763, based on ALZA Corporation's manufacturing and selling of Doxil® and Caelyx®. Doxil® is currently approved and marketed in the United States for Kaposi's sarcoma and refractory ovarian cancer by Ortho Biotech, a subsidiary in the Johnson & Johnson family of companies. The same product, Caelyx® is approved and marketed in Europe for the same indications by Schering Plough.

        President and CEO, Dr. Benjamin F. McGraw, III stated, "We believe the grant of this European patent further substantiates the value of this patent family, following as it does the grant of similar broad patent claims in the United States and Japan. We continue to believe in the importance of protecting our intellectual property, and have therefore found it necessary to file infringement proceedings in Germany."

        Liposomes are microscopic vesicles composed of a phospholipid bilayer that are capable of encapsulating active drugs. PEGylation of liposomes modifies their clearance and biodistribution after systemic administration, enhancing tumor localization and reducing non-specific uptake in normal tissues.

        Earlier this year the Company announced that it was suspending clinical development of its cancer immunotherapy products following release of clinical data from a Phase II clinical trial of an IL-2 GeneMedicine™ product. Consistent with these developments and a decision by partner Roche Holdings Ltd. not to initiate a Phase III clinical trial, the Company's alliance with Roche has ended in accordance with terms of the agreement. The Company will continue to focus on the development of its del-1 GeneMedicine™ product for the treatment of peripheral arterial disease and ischemic heart disease, and preclinical discovery efforts on its GeneSwitch™ and OptiPEG™ technologies.

        Valentis is Converting Genomic Discoveries into Medicines™. The Company has three product platforms for the development of novel therapeutics: the GeneMedicine™, GeneSwitch® and OptiPEG™ platforms. The Del-1 GeneMedicine™ therapeutic is the lead product for the GeneMedicine™ platform of non-viral gene delivery technologies. Del-1 is an angiogenesis gene that is being developed for peripheral arterial disease and ischemic heart disease. The EpoSwitch™ therapeutic for anemia is the lead product for the GeneSwitch® platform. The EpoSwitch™ product is being developed to allow control of erythropoietin protein production from an injected gene by an orally administered drug. The OptiPEG™ platform, consisting of proprietary PEGylation technologies, allows for improved dosing of biopharmaceuticals. OptiPEG™ is being developed through licensing to partners. Additional information is available at www.valentis.com.

        Statements in this press release that are not strictly historical are "forward-looking" statements as defined in the Private Securities Litigation Reform Act of 1995. The words "believes," "expects," "intends," "anticipates," variations of such words, and similar expressions identify forward-looking statements, but their absence does not mean that the statement is not forward-looking. These



statements are not guarantees of future performance and are subject to certain risks, uncertainties and assumptions that are difficult to predict. Factors that could affect Valentis' actual results include the need for additional capital, the early stage of product development, uncertainties related to clinical trials, and uncertainties related to patent position. There can be no assurance that Valentis will be able to develop commercially viable gene-based therapeutics or PEGylated biopharmaceuticals, that any of the Company's programs will be partnered with pharmaceutical partners, that necessary regulatory approvals will be obtained, or that any clinical trial will be successful. Actual results may differ from those projected in forward-looking statements due to risks and uncertainties that exist in the company's operations and business environments. These are described more fully in the Valentis Annual Report on Form 10-K for the period ended June 30, 2001 and Quarterly Report on Form 10-Q/A for the period ended December 31, 2001, each as filed with the Securities and Exchange Commission.




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VALENTIS ANNOUNCES ISSUANCE OF PEGYLATED LIPOSOMES PATENT IN EUROPE, INITIATION OF INFRINGEMENT SUIT, AND ONCOLOGY PROGRAM UPDATE
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