Company Profile

Sangamo Therapautics Inc (AKA: Sangamo BioSciences Inc)
Profile last edited on: 2/7/23      CAGE: 46C88      UEI: TQ1RZLQNJ5H6

Business Identifier: Genome editing, gene therapy, gene regulation and cell therapy
Year Founded
1995
First Award
1996
Latest Award
2006
Program Status
Inactive
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Location Information

501 Canal Boulevard Suite A100
Richmond, CA 94804
   (510) 970-6000
   busdev@sangamo.com
   www.sangamo.com
Location: Multiple
Congr. District: 11
County: Contra Costa

Public Profile

Originally founded as Sangamo BioSciences, Inc. organized around developing new technologies for genome editing, Sangamo Therapeutics, Inc. (NASDAQ:SGMO) is clinical stage biopharmaceutical company, focuses on translating ground-breaking science into genomic therapies that transform patients' lives using platform technologies in genome editing, gene therapy, gene regulation, and cell therapy. The company’s proprietary zinc finger DNA-binding protein (ZFP) technology enables specific genome editing and gene regulation. The ZFPs could be engineered to make ZFP nucleases (ZFNs), proteins that could be used to specifically modify DNA sequences by adding or knocking out specific genes; and ZFP transcription factors (ZFP TFs), proteins that can be used to turn genes on or off. Its therapeutic products include SB-728-T, a ZFN-mediated autologous T-cell product for human immunodeficiency virus and acquired immunodeficiency syndrome (HIV/AIDS), which is in Phase II and Phase I clinical trials; and SB-728-HSPC that is in Phase I/II clinical trials for HIV/AIDS. The company also engages in Phase I/II studies of in vivo genome editing applications of ZFP Therapeutics for hemophilia B, Hemophilia A, and Mucopolysaccharidosis I (MPS) and MPS II, which are lysosomal storage disorder (LSD); proprietary preclinical programs in other LSDs; and research stage programs in certain central nervous system disorders and cancer immunotherapies. It has collaborative partnerships with Biogen Inc. to develop therapeutic genome editing products in hemoglobinopathies; and with Shire International GmbH to develop the preclinical development program in Huntington’s disease, as well as license agreement with Sigma-Aldrich Corporation to develop ZFP-based laboratory research reagents and Dow AgroSciences, LLC to modify the genomes or alter protein expression of plant cells, plants, or plant cell cultures.

Extent of SBIR involvement

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Synopsis: Awardee Business Condition

Employee Range
150-249
Revenue Range
15M-20M
VC funded?
Yes
Public/Private
Publicly Traded
Stock Info
NASDAQ : SGMO
IP Holdings
250-500

Awards Distribution by Agency

Most Recent SBIR Projects

Year Phase Agency Total Amount
2006 1 NIH $100,000
Project Title: ZFN-driven Gene Disruption of CCR5 as a Potential Treatment of AIDS
2004 1 NIH $104,000
Project Title: Using Enhanced Gene Targeting to Repair the Sickle Cell
2003 2 NIH $475,604
Project Title: Targeted VEGF Methylation: Novel Cancer Therapy
2000 1 NIH $99,970
Project Title: Blocking Heparanase Transcription to Control Metastasis
2000 1 NIH $99,775
Project Title: Transcription Repressors to Analyze Cancer Genes

Key People / Management

  Edward O Lanphier II -- President; Chief Executive Officer

  Dale Ando -- Vice President, Therapeutic Development; Chief Medical Officer

  Ely Benaim -- Vice President, Clinical Affairs

  Bruce P Burnett

  Judith Campisi

  C Case

  Stephen P Eisenberg

  Philip D Gregory -- Vice President, Research; Chief Scientific Officer

  Curt Herberts -- Senior Vice President

  David G Ichikawa -- Senior Vice President, Business Development

  Andrew C Jamieson

  Eric Jarvis

  Qiang Liu

  Geoffrey Nichol -- Executive Vice President, Research and Development

  Carl O Pabo

  Hong Qi

  Edward Rebar

  Eric Rhodes -- Vice President of Business Development and Alliance Management

  Sharon K Spratt

  Fyodor D Urnov

  Ward Wolff -- Executive Vice President; Chief Financial Officer