Annual Meeting and Investor Day
May 25, 2017
Annual Meeting and Investor Day May 25, 2017 Meeting Agenda May - - PowerPoint PPT Presentation
Annual Meeting and Investor Day May 25, 2017 Meeting Agenda May 25th 8:00 8:30am Annual Shareholders Meeting Analyst/Investor Day Presentations 8:30 9:15am CEO Review 9:15 10:00am Pathologist Perspective 10:00 10:15am
May 25, 2017
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8:00 – 8:30am Annual Shareholders Meeting Analyst/Investor Day Presentations 8:30 – 9:15am CEO Review 9:15 – 10:00am Pathologist Perspective 10:00 – 10:15am Break 10:15 – 11:00am Pharma Services 11:00 – 12:00am R&D and New Test Development Noon - 1:00pm Lunch/Review of Governmental Affairs 12:10pm – 1:30pm- Lab Tours – leaving every 20 minutes
May 25, 2017
May 25, 2017
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8:00 – 8:30am Annual Shareholders Meeting Analyst/Investor Day Presentations 8:30 – 9:15am CEO Review 9:15 – 10:00am Pathologist Perspective 10:00 – 10:15am Break 10:15 – 11:00am Pharma Services 11:00 – 12:00am R&D and New Test Development Noon - 1:00pm Lunch/Review of Governmental Affairs 12:10pm – 1:30pm- Lab Tours – leaving every 20 minutes
This presentation contains statements which constitute forward-looking statements within the meaning of Section 27A of the Securities Act, as amended; Section 21E of the Securities Exchange Act of 1934; and the Private Securities Litigation Reform Act of 1995. The words “may”, “would”, “could”, “will”, “expect”, “estimate”, “anticipate”, “believe”, “intend”, “plan”, “goal”, and similar expressions and variations thereof are intended to specifically identify forward-looking statements. All statements that are not statements of historical fact are forward-looking statements. Investors and prospective investors are cautioned that any such forward-looking statements are not guarantees of future performance and involve risks and uncertainties, and that actual results may differ materially from those projected in the forward-looking statements as a result of various
and Exchange Commission. We undertake no obligation to publicly update or revise the forward looking statements made in this presentation to reflect events or circumstances after the date of this presentation or to reflect the occurrence of unanticipated events.
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Douglas VanOort
Chairman & CEO
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By providing uncompromising quality, exceptional service and innovative solutions, we will be the World’s leading cancer testing and information company.
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Clinical Genetic Testing Annual Revenue Clinical Genetic Tests Performed
($, 000s) * Base NEO represents organic revenue and test volume growth from legacy business and excludes the impacts from the PathLogic and Clarient acquisitions.
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$558 $1,885 $6,476 $11,505 $20,015 $29,469 $34,371 $43,484 $59,866 $66,467 $82,194 $188,374 $214,708
2004 2005 2006 2007 2008 2009 2010 2011 2012 2013 2014 2015 2016 Pro Forma Clarient 2015 Genetic Test Revenue NEO Clinical Genetic Testing Revenue
1,152 4,082 12,838 20,998 32,539 45,675 57,332 76,288 114,606 137,317 177,279 490,450 563,132
2004 2005 2006 2007 2008 2009 2010 2011 2012 2013 2014 2015 2016 Pro Forma Clarient 2015 Clinical Genetic Tests NEO Clincial Genetic Tests Performed
Confidential
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Key Benefits Outstanding Customer Mix Similar Product Lines (1)
IHC 42% FISH/ISH 19% FLOW 14% Molecular 15% Cyto 5% Other 5%
(1) Clinical operations only. Percentage of tests Performed.
SIMILAR CLINICAL CUSTOMERS (About 2,400) New BIOPHARMA CUSTOMERS (200 Projects with >30 Customers)
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The Deal – Closed on 12/30/15
shares of NEO, $110mm Pfd. Stock.
$20.7 $23.2 $25.0 $23.0 $24.4 $25.1 $26.6 $30.3 $32.4 $31.8 $35.9 $61.7 $0.7 $29.4 $30.7 $28.9 $24.6
$0 $10 $20 $30 $40 $50 $60 $70 Q2 14 Q3 14 Q4 14 Q1 15 Q2 15 Q3 15 Q4 15 Q1 16 Q2 16 Q3 16 Q4 16 Q1 17
Quarterly Revenue
(millions) Clarient Rev Neo Rev
Revenue up 29% over 6 quarters pre-acquisition Revenue flat during Integration
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After 15 months, as of March 31, 2017, Integration is 100% complete.
After 16 months, Client Retention is nearly 100%.
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Same historically successful attributes :
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Growth Goals:
Driven by:
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Market was $5.1B in 2014
Market is about $6B in 2017
expected to consolidate further over time
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Large Reference Labs LabCorp Quest Diagnostics BioReference/OPKO Myriad Genetics Eurofins Pure-Play Comprehensive Oncology Labs NeoGenomics Genoptix CSI PhenoPath Various Regional Players Specialty Labs Exact Sciences Foundation Medicine Genomic Health Natera Invitae Veracyte Fulgent Genetics Large Academic Centers, Hospitals, and Other ARUP Mayo MD Anderson Memorial Sloane Kettering Others Estimated $2.5 Billion in Oncology Testing Approximately $1.1 Billion in Oncology Testing Approximately $2 Billion in Oncology Testing About 20 M&A and Strategic Initiatives over past 12 months Approximately $500 million in Oncology Testing Combined Adjusted EBITDA loss for 2017 of $450 million NeoGenomics now largest and most profitable player
Recent Consolidators Avg growth 30%+ Significant Change Ocurring
Source: National Institutes of Health (NIH)
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increases with age
treatments lead to more survivors and monitoring
targeted therapeutics
more careful triage
Shifting De mogr aphic s Inc ide nc e of Canc e r by Age
0.0 20.0 40.0 60.0 80.0 100.0 120.0 Ag e 60- 64 Ag e 65- 74 Ag e 75- 84 Ag e 85+ 1.0% 2.7% 5.1% 13.8% 24.4% 26.2% 18.8% 7.9% < 20 20- 34 35- 44 45- 54 55- 64 65- 74 74- 84 > 84
So urc e : Unite d Sta te s Ce nsus Bure a u So urc e : Na tio na l Ca nc e r I nstitute
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Therapeutic Area Drug Examples Example Companion or Complimentary Tests
Immuno-Oncology Keytruda, Opdivo, and many in development PD-L1, MSI, MMR, Tumor Mutation Burden (TMB) NSCLC Anti-EGFR, ALK inhibitors, etc. EGFR, ALK, ROS1, BRAF V600E, MET, RET, NTRAK, etc. Ovarian and Prostate PARP Inhibitors BRCA, PTEN, ERG, MMR, Breast and Gastric Herceptin HER2/neu IHC & FISH tests, BRCA, and numerous molecular tests Melanoma Vemurafenib (Zelboraf) BRAF, C-KIT, numerous FISH tests
70 ne w/ re vise d te sts:
Ne oL AB
T M Liquid Biopsie s
Pro file
Pro file
L T 3 Muta tio n Ana lysis
ra nslo c a tio n
1T ra nslo c
NV16 T ra nslo c a tio n
DH1 Muta tio n Ana lysis
DH2 Muta tio n Ana lysis
RAS Muta tio n Ana lysis
K I nhib ito r Re sista nc e
umo r Mo nito ring
Ge rmline MolDx T e sting
ync h Synd ro me (c o lo n)
Pre d isp o sitio n Pa ne l
Othe r
K , ROS1, RE T F usio n
usio n
T E Ce rvic a l F I SH
xp a nd e d I HC Me nu
lo w Cyto me try
lo w Cyto me try
mp le me nte d Ad v Mo lDx p la tfo rm in lie u o f K its
inc re a sing se nsitivity o f Sa ng e r se q ue nc ing
YPE Mo lDx Pa ne ls
I SH (Pa te nt Ap p )
so p h. F I SH (Pa te nt Ap p )
nte rna lize d se nd -o uts
40 ne w/ re vise d te sts:
YPE Pa ne ls
Se q ue nc ing (48 g e ne s)
I SH
T E Me la no ma F I SH
T e st (Pa te nt Ap p )
Ana lysis Syste m
I SH Ana lysis Syste m v2
Ne o L AB (L iq uid Alte rna tive to Bio p sy) Pro sta te Cx te st
60 ne w/ re vise d te sts:
YPE Ne xt Ge ne ra tio n Se q ue nc ing Pro file s
HC/ I SH te sts
AB Pro sta te c linic a l stud ie s
E xte nd e d F I SH Pa ne l
F a vo ra b le -Risk F I SH Pa ne l
xte nd e d F I SH Pa ne l
Stra tific a tio n F I SH Pa ne l
T F I SH
T F I SH
L Ad ult & Pe d ia tric F I SH Pa ne ls
R2 Bre a st E q uivo c a l F I SH Pa ne l
T ra nslo c a tio n F I SH
a unc he d ro b o tic F I SH-Cyto p ro c e ssing p la tfo rm
50 ne w/ re vise d te sts:
1 T e sting (thre e F DA-c le a re d a nd o ne L DT )
Ca nc e r NGS F usio n, Muta tio n a nd E xp re ssio n Pro filing .
lo w Cyto me try d a ta a na lysis p la tfo rm
nhe rite d Bo ne Ma rro w F a ilure
T E xo n 14 De le tio n Ana lysis
xo n 4 Muta tio n Ana lysis
K , NT RK , RE T , ROS1 F usio n
Ne oL AB
T M Liquid Biopsie s
AB Mye lo id Diso rd e rs Pro file
GF R T 790M
Ne oT YPE
T M Multi Modality Profile sT L / Pe rip he ra l T
ymp ho ma
hyro id Pro file
umo r Pro file
ip o sa rc o ma F usio n Pro file
umo r Pro file
F ISH & IHC
I SH T e sting fo r E WSR1, SS18, DDI T 3, ST AT 6, BCL 2, & T CL 1
HC T e sting fo r CXCL 13, BAP1, I NI 1, MUC4
2012 2013 2014 2015 2016
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Pathologists & Hospitals (about 80% of Revenue)
Oncologists, Hematologists & Clinicians (about 10% of Revenue)
Pharma Services & Other (about 10% of Revenue)
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“Old Clarient Clients” Great reputation – Solid Tumors
– FISH – great solid tumor FISH
franchise, good capacity
– Flow Cytometry – excellent program,
expandable capacity
– Cytogenetics – good product and
service
– Digital Imaging and IHC –
steady volume
“Old NEO Clients” Great reputation - Heme Cancers
– FISH – outstanding hemeFISH
franchise, good capacity
– Flow Cytometry – Outstanding
program, expandable capacity
– Cytogenetics – outstanding product
and service
– Molecular – unique product, fast
growing volume
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2015 Adjusted EBITDA NeoGenomics $ 9.7 MM Clarient Pro Forma $ 9.2 MM Pro Forma Combined $18.9 MM 2016 “New Neo” EBITDA $ 34.7 MM
Clearly, “synergies” showed up in 2016 --- and there are more to be realized in 2017- 18 2017 – 2018 Opportunities:
9 + 9 equals 34
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* To facilitate comparison, all data is for Clinical Genetic Testing and excludes the impact from the PathLogic acquisition and Pharma Services. (1) Productivity calculated as the average number of lab tests completed per month per laboratory FTE.
45.9% 44.7% 44.8% 47.7% 48.0% 46.1% 47.2%
65.6%
0% 10% 20% 30% 40% 50% 60% 70% 35% 40% 45% 50% 55% 2010 2011 2012 2013 2014 2015 2016 Gross Margin % From Clinical Genetic Testing Cum Change in Avg Rev/ Clinical Genetic Test Since 2009 Cum Change in Productivity Since 2009
Cum Change in Avg Rev/Test & Productivity
(1) 26
$41.6mm Backlog as of 3/31/17 - Approx. 400 active projects from 100+ Clients
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Confidential 28
NEO Focus – Upper right hand quadrant Synergistic Deals
High High Low Market Growth Technologies
NextGen Seq Digital Companion Dx Pathology Oncology FISH Clinical Trials Flow Cytogenetics Traditional Anatomic Path. BioInformatics
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Requirements
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May 2012 $1.67
By providing uncompromising quality, exceptional service & innovative solutions, we will be the world’s leading cancer testing and information company!
15%+
Clinical Volume CAGR
20%+
Pharma Services Revenue CAGR
20-25%
Adjusted EBITDA Margins
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Unique and leading pure-play Oncology Company History of strong performance Significant opportunities for growth Realization of cost synergies expected to accelerate Strategic opportunities highly likely over the next 36 mos Well positioned for continued Industry Leadership
Questions and Answers
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