© 2011 fluxion biosciences. all rights reserved. brief timeline and flunding history

11
© 2011 Fluxion Biosciences. All rights reserved. Brief timeline and flunding history

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Page 1: © 2011 Fluxion Biosciences. All rights reserved. Brief timeline and flunding history

© 2011 Fluxion Biosciences. All rights reserved.

Brief timeline and flunding history

Page 2: © 2011 Fluxion Biosciences. All rights reserved. Brief timeline and flunding history

Page 2© 2011 Fluxion Biosciences. All rights reserved.

Fluxion today

BioFlux 200 BioFlux 1000 IonFlux-16 IonFlux HT

• Company:– Venture backed since Dec 2007– 4 products commercialized and selling globally– Segment: Biotools– Over 100 units installed

• Products: instruments and consumables– BioFlux System for cell-cell interactions– IonFlux Automated Patch Clamp System– IsoFlux rare cell isolation platform – under development

Page 3: © 2011 Fluxion Biosciences. All rights reserved. Brief timeline and flunding history

Page 3© 2011 Fluxion Biosciences. All rights reserved.

Partial customer list

Johnson & Johnson

Page 4: © 2011 Fluxion Biosciences. All rights reserved. Brief timeline and flunding history

Page 4© 2011 Fluxion Biosciences. All rights reserved.© 2011 Fluxion Biosciences. All rights reserved.

IonFlux applications

• Compound profiling– Dose response measurements– Hit confirmation– Single concentration screening

• Mutant screening – Evaluate functional changes dependent on mutations– Record responses from up to 32 distinct mutants (8 for IF-HT)

• Structure-function studies– Determine the effect of mutations on channel function– Characterize expression for differentiated stem cells– Recording endogenously expressed ion channels– Screen clones based on ion channel density

Page 5: © 2011 Fluxion Biosciences. All rights reserved. Brief timeline and flunding history

Page 5© 2011 Fluxion Biosciences. All rights reserved.© 2011 Fluxion Biosciences. All rights reserved.

IonFlux Technology for APC- Best in Class

• High quality data– G-seal quality recordings– Ensemble recording for improved

success rate

• Cost effective– Perform APC for about the cost of an

MPC setup

• Simple to use– Ease of use of a ‘plate reader’– Relevance of patch clamp data– Table top unit

• Reliable– No robotics required– Only two moving parts

Page 6: © 2011 Fluxion Biosciences. All rights reserved. Brief timeline and flunding history

Page 6© 2011 Fluxion Biosciences. All rights reserved.

Ensemble vs. single cell recording

• Ensembles average signals over 20 patched cells (16 ensembles per plate, left panel)

• The new single cell consumable records from one cell per channel (16 cells per plate for IF-16, right panel)

• The single cell consumable utilizes the same hardware

20-cell ensemble Single cell

Page 7: © 2011 Fluxion Biosciences. All rights reserved. Brief timeline and flunding history

Page 7© 2011 Fluxion Biosciences. All rights reserved.© 2010 Fluxion Biosciences. All rights reserved.

Well-Plate Integrated Microfluidics

Well-plate integrated microfluidics (WPM) utilizes standard 96- and 384-well plates, but the bottom of the plate is replaced with a microfluidic network interconnected between the wells.

Page 8: © 2011 Fluxion Biosciences. All rights reserved. Brief timeline and flunding history

Page 8© 2011 Fluxion Biosciences. All rights reserved.

* Sample customer slide – Pfizer UK

Page 9: © 2011 Fluxion Biosciences. All rights reserved. Brief timeline and flunding history

Page 9© 2011 Fluxion Biosciences. All rights reserved.© 2011 Fluxion Biosciences. All rights reserved.

High Level Timeline

Founded

2006 2007 2008 2009 2010 2011

Grant 1 Ph2

Grant 1 Ph1

Grant 2 Ph2

Grant 2 Ph1

BioFlux product launch

IonFlux product launch

Series A Series B

Page 10: © 2011 Fluxion Biosciences. All rights reserved. Brief timeline and flunding history

Page 10© 2011 Fluxion Biosciences. All rights reserved.© 2011 Fluxion Biosciences. All rights reserved.

Grant pipeline and success rates

Page 11: © 2011 Fluxion Biosciences. All rights reserved. Brief timeline and flunding history

Page 11© 2011 Fluxion Biosciences. All rights reserved.

SBIR: the good, the bad and the ugly

• The good:– Non-dilutive capital!– Can be the catalyst for new projects, encourages innovation– Early $$, which are the hardest

• The bad:– Long timelines: 9 mo. from application to funding– <200k is low capital for Phase I awards– Can be a distraction from the central mission

• The ugly:– Review process dependent on random events– In our case, projects with the greatest commercial worth didn’t get funded