UNITED STATES
                       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


Date of Report (Date of earliest event reported):  December 19, 2008
                                                   ------------------

                            SANGAMO BIOSCIENCES, INC.
               (Exact name of registrant specified in its charter)


           Delaware                      000-30171               68-0359556
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(State or other jurisdiction     (Commission File Number)    (I.R.S. Employer
      of incorporation)                                      Identification No.)


501 Canal Blvd, Suite A100, Richmond, California        94804
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(Address of principal executive offices)              (Zip Code)


Registrant's telephone, including area code:  (510) 970-6000
                                              --------------


- --------------------------------------------------------------------------------
         (Former name and former address, if changed since last report)


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simultaneously  satisfy the filing obligation of the registrant under any of the
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(17 CFR 230.425)

      |_| Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17
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      |_|  Pre-commencement  communications  pursuant to Rule 14d-2(b) under the
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      |_|  Pre-commencement  communications  pursuant to Rule 13e-4(c) under the
Exchange Act (17 CFR 240.13e-4(c))



ITEM 1.01. ENTRY INTO A MATERIAL DEFINITIVE AGREEMENT. On December 19, 2008, Sangamo BioSciences, Inc. ("Sangamo") entered into a License Agreement with Pfizer Inc. ("Pfizer"), pursuant to which Sangamo provided Pfizer with a limited right to use Sangamo's proprietary zinc-finger nuclease ("ZFN") technology. Under this agreement, Pfizer received a worldwide, fully paid, perpetual, royalty free, non-exclusive license to use certain ZFN reagents for the elimination of the Glutamine Synthetase gene in Pfizer's Chinese Hamster Ovary ("CHO") cell lines and to use such ZFN-modified CHO cells for clinical and commercial production of therapeutic protein products. The license may not be sublicensed although Pfizer may transfer any ZFN-modified CHO cell lines to a contract manufacturer solely for such contract manufacturer to manufacture Pfizer's therapeutic proteins for Pfizer. Sangamo will receive an upfront payment of $3.0 million from Pfizer which constitutes full and complete payment for the license. ITEM 7.01 REGULATION FD DISCLOSURE On December 22, 2008, Sangamo issued a press release announcing the transaction described in Item 1.01 above. A copy of the press release is attached as Exhibit 99.1 hereto and is incorporated herein by reference. ITEM 9.01. FINANCIAL STATEMENTS AND EXHIBITS. (d) Exhibits. The following document is filed as exhibit to this report: 99.1 Press Release of Sangamo Biosciences, Inc., dated December 22, 2008

SIGNATURES Pursuant to the requirements of the Securities Exchange Act of 1934, as amended, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized. SANGAMO BIOSCIENCES, INC. Date: December 22, 2008 By: /s/ EDWARD O. LANPHIER II ---------------------------------- Name: Edward O. Lanphier II Title: Chief Executive Officer

                                                                    EXHIBIT 99.1

[GRAPHIC OMITTED]


                                                       Sangamo BioSciences, Inc.
                                                      Point Richmond Tech Center
                                                             501 Canal Boulevard
                                                             Richmond, CA  94804
                                                510-970-6000 o 510-236-8951(Fax)

   SANGAMO BIOSCIENCES ANNOUNCES LICENSE AGREEMENT WITH PFIZER FOR ZINC FINGER
                        NUCLEASES FOR PROTEIN PRODUCTION

        License Permits Use of ZFN Reagents to Knock Out Gene in Protein
                                Production Cells

      RICHMOND,  Calif., Dec. 22  /PRNewswire-FirstCall/ -- Sangamo BioSciences,
Inc. (Nasdaq:  SGMO), the leading developer of zinc finger DNA-binding  proteins
(ZFPs),  today  announced an agreement to provide Pfizer Inc (NYSE:  PFE) with a
worldwide,  non-exclusive  license  for the use of certain ZFP  Nuclease  (ZFNs)
reagents to permanently  eliminate the Glutamine Synthetase (GS) gene in Chinese
Hamster Ovary (CHO) cell lines and for the use of these  ZFN-modified  cells for
clinical and commercial production of therapeutic  proteins.  Under the terms of
the  agreement  Sangamo  will  receive an upfront  payment of $3.0  million from
Pfizer for a fully paid license.

      "Pfizer was an early  adopter of  Sangamo's  ZFN  technology  for CHO cell
engineering," said Edward Lanphier, Sangamo's president and CEO. "Our colleagues
at Pfizer  have made  fundamental  contributions  to  establish  the breadth and
utility of ZFNs in cell line engineering.  We are very pleased to establish this
non-exclusive,  commercial  protein production license providing Pfizer with the
right to use ZFNs to eliminate the GS gene in CHO cells, a widely used selection
marker for the  generation of cell lines used for the  production of recombinant
protein  pharmaceuticals  and monoclonal  antibodies.  Based upon our ability to
design ZFNs to any gene,  we believe that this is one of many future  agreements
we may establish,  applying our ZFN  technology in the commercial  production of
protein-based pharmaceuticals."

      "We are very  pleased to enter  into this  commercial  protein  production
license agreement with Sangamo. Together we've used ZFNs to generate specific GS
knockouts in CHO cells to streamline the creation of mAb production cell lines,"
said David Brunner,  Vice President,  Bioprocess Research & Development,  Pfizer
Global  Biologics.   "We  have  generated   significant   research  and  process
development data following application of the ZFN platform technology.  ZFNs can
be used to eliminate  genes and potentially  improve culture  performance or the
characteristics of therapeutic proteins being manufactured."

      "Prior to the development of ZFN  technology,  methods for gene disruption
were limited by their  efficiency,  time to  completion,  and the  potential for
confounding,  off-target effects," said Philip Gregory, D.Phil.,  Sangamo's Vice
President for Research.  "We have demonstrated the power and broad applicability
of  our  ZFN  technology  in  the   engineering  of  living  cells  in  multiple
publications  in  high-impact,  peer-reviewed  journals.  Earlier  this  year we
published  work  describing  a rapid,  single-step  approach  to  targeted  gene
knockout   in   mammalian   cells  using  ZFNs  (Proc  Natl  Acad  Sci  U  S  A.
2008;105):5809-14).  We have  demonstrated  that  we can  achieve  a  permanent,
heritable  elimination  of a gene giving a true  knockout of that gene in a cell
and all of its progeny. Our ZFN process is simple, rapid and highly specific and
does not  require  marker  genes or the  permanent  insertion  of  foreign  DNA.
Moreover,  this is not limited to a single gene in a cell;  our ZFNs can be used
to generate a cell line in which multiple genes are selectively and specifically
eliminated.  We have been working with  scientists  at Pfizer to establish  that
this process is  compatible  with  suspension  growth in  serum-free  and animal
component-free  synthetic  media which is an  important  consideration  in human
therapeutic  protein  manufacturing.  Our  work  also  confirms  that  ZFNs  are
highly-specific;  we have not  observed  any  negative  impact  on cell  growth,
protein production yield or product characteristics."


Terms of the Agreement Under this agreement, Sangamo will provide a worldwide, fully paid, perpetual, royalty free, non-exclusive, license for the use of certain ZFN reagents for the elimination of the GS gene in Pfizer's CHO cell lines and to use such ZFN-modified CHO cells for clinical and commercial production of therapeutic protein products. Sangamo will receive an upfront payment of $3.0 million from Pfizer which constitutes full and complete payment for the license. The license may not be sublicensed although Pfizer may transfer any GS ZFN-modified CHO cell line to a contract manufacturer solely for such contract manufacturer to manufacture Pfizer's therapeutic proteins for Pfizer. About Sangamo BioSciences, Inc. Sangamo BioSciences, Inc. is focused on the research and development of novel DNA-binding proteins for therapeutic gene regulation and modification. The most advanced ZFP Therapeutic(TM) development program is currently in Phase 2 clinical trials for evaluation of safety and clinical effect in patients with diabetic neuropathy and ALS. Other therapeutic development programs are focused on HIV/AIDS, neuropathic pain, cancer, nerve regeneration and monogenic diseases. Sangamo's core competencies enable the engineering of a class of DNA-binding proteins known as zinc finger DNA-binding proteins (ZFPs). By engineering ZFPs that recognize a specific DNA sequence Sangamo has created ZFP transcription factors (ZFP TF(TM)) that can control gene expression and, consequently, cell function. Sangamo is also developing sequence-specific ZFP Nucleases (ZFN(TM)) for therapeutic gene modification as a treatment for a variety of monogenic diseases, such as X-linked SCID and hemophilia, and for infectious diseases, such as HIV. Sangamo has established strategic partnerships with companies outside of the human therapeutic space including Dow AgroSciences, Sigma-Aldrich Corporation and several companies applying its ZFP technology to enhance the production of protein pharmaceuticals. For more information about Sangamo, visit the company's web site at http://www.sangamo.com/. This press release may contain forward-looking statements based on Pfizer's and Sangamo's current expectations. These forward-looking statements include, without limitation, the application of the ZFN technology in the engineering of living cells and absence of negative effects on ZFN engineered cells. Actual results may differ materially from these forward-looking statements due to a number of factors, including technological challenges, ability of Sangamo and Pfizer to develop commercially viable products and technological developments by our competitors. See the company's SEC filings, and in particular, the risk factors described in the company's Annual Report on Form 10-K and its most recent Quarterly Report on Form 10-Q. Sangamo assumes no obligation to update the forward-looking information contained in this press release. Contact Sangamo BioSciences, Inc. Elizabeth Wolffe, Ph.D. 510-970-6000, x271 ewolffe@sangamo.com ###