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8-K - FORM 8-K - SOLTA MEDICAL INC | d239840d8k.htm |
Pending Acquisition of
LipoSonix October 5, 2011
Exhibit 99.1 |
2
Forward Looking Statements
This presentation contains forward-looking statements within the meaning of the U.S.
Private Securities Litigation Reform Act of 1995. Examples of such
forward-looking statements include, but are not limited to, anticipated timing of
U.S. Food and Drug Administration and European Union clearance of the second generation of the
LIPOSONIX system, projected likelihood and amount of contingent payments and anticipated
cost savings, synergies and other opportunities. Forward-looking statements are
based on management's current expectations and are subject to risks and
uncertainties, which may cause actual results to differ materially from the statements
contained herein. Factors that might cause such a difference include the risk that sales of
the LIPOSONIX product line do not grow (or grow less than anticipated), risks arising
in connection with the achievement of applicable regulatory clearances and risks
relating to timing and successful completion of technology and product
development. Further information on potential risk factors that could affect Solta
Medicals business and its financial results are detailed in its Form 10-K
as effective March 16, 2011 and other reports as filed from time to time with the
Securities and Exchange Commission. Undue reliance should not be placed on forward-looking
statements, which speak only as of the date they are made. Solta Medical undertakes no
obligation to update publicly any forward-looking statements to reflect new
information, events or circumstances after the date they were made, or to reflect the
occurrence of unanticipated events. Management has provided non-GAAP gross
profit, non-GAAP operating income (loss), non-GAAP EBITDA, non-GAAP net income
(loss) and non-GAAP earnings (loss) per share measures that exclude the impact of
purchase price related adjustments, severance costs, and stock-based compensation
expenses, all net of income taxes. The Company believes that these non- GAAP
financial measures provide investors with insight into what is used by management to conduct a more
meaningful and consistent comparison of the Company's ongoing operating results and trends,
compared with historical results. A reconciliation of the differences between the
non-GAAP financial measures and the most comparable financial measures presented
in accordance with GAAP can be found in the Investor Relations section of the
Companys website (www.solta.com). |
LipoSonix Meets Key
Acquisition Criteria
GAAP/Non-GAAP EPS accretive within a year
Gross margin > 60%
Strong recurring revenue component to business model
Same call point
Unique innovative technology
Key Acquisition Criteria
3 |
4
Initial Consideration
$15,000,000
Cash payment
FDA Clearance of Gen 2
LipoSonix product
$20,000,000
Payment due upon Gen 2 FDA clearance, assumed end of Q1 2012
Payment reduced if Gen 2 FDA clearance comes after April 2012
Additional Annual
Contingent Payments
1
Contingent
2
100% of the incremental increase in year-over-year net sales of
transducers related to the LipoSonix product
100% of the incremental increase in year-over-year gross profit on
LipoSonix product systems
Duration of Contingent
Payments
Seven years from U.S. commercialization
LipoSonix Transaction Analysis
(1) An additional contingent payment of $30 million will be required to be made by Solta
following the first year in which net sales/gross profits of LipoSonix products exceed $300
million.
(2) 75% of the Incremental year-over-year net sales and gross profits will be paid to
LipoSonix shareholders under the LipoSonix Agreement and under certain circumstances would be
payable to Medicis, and 25% of the Incremental year-over-year net sales and gross profits will be paid to Medicis under the Medicis Agreement. The definition of
LipoSonix product differs between the two agreements. In addition to all products covered in the
LipoSonix Agreement, the Medicis Agreements definition includes all products that apply
HIFU and incorporate LipoSonix technology. |
5
LipoSonix Transaction Analysis (cont.)
In year 1, the contingent payment will represent a significant
percentage of total sales
In year 2, the contingent payment as a percentage of total sales
will likely fall substantially
By year 7, the contingent payment as a percentage of total sales
will likely look more like a royalty payment
Based on our estimates, the aggregate consideration paid will
likely range between 1.5x to 1.0x revenues. The revenue
multiple will approach 1.0x, the better the LipoSonix acquisition
performs. |
6
Investment Highlights
Targeting aesthetic and permanent reduction in fat tissue (body contouring), next
key market opportunity in aesthetics
Clinically proven results supported by scientific fundamentals
Proprietary High-Intensity Focused Ultrasound (HIFU) technology
with over 15 issued patents and 27 pending applications in the U.S. and 168
issued or pending patents internationally
Anticipate launch of second generation technology in Q4:2011 internationally and
early 2012 in the U.S.
Compelling physician economics that draw new entrants
Attractive recurring revenue and high margin business model
Strong opportunities for growth in expanding markets and new indications
|
7
Compelling Transaction Rationale
Strategic Rationale
Financial Rationale
Targets the same customer base
Large, new, growing market opportunity
Adds another highly differentiated
technology to the Solta platform
Highly complementary consumables
business model
Projected gross margins of over 60%
GAAP/Non-GAAP EPS accretive within 12
months
Opportunity to leverage Soltas sales,
marketing and corporate infrastructure
Growth Opportunities
Large, new aesthetic body contouring market creates short, medium and
long-term growth opportunity for Solta
Opportunity to utilize Soltas premier distribution platform in the U.S. and
internationally
LipoSonix to benefit from Soltas unique brand building marketing
organization
Ability to enhance Soltas pipeline of innovative and differentiated
products |
8
Aesthetic and Permanent Reduction in Fat Tissue (Body Contouring):
The Next Growth Driver in Aesthetics
Aesthetic body contouring device market is the next key device market in aesthetics
and
has
a
projected
CAGR
of
17.7%
3
Access to physicians
increasing
due to penetration into medical spas and non-core
physician markets
Over
215,000
liposuction
and
tummy
tucks
performed
in
2010
4
Aesthetic
body
contouring
devices
may
add
the
finishing
touches
to
any
weight
loss
bid
(3) iData Research Aesthetic Laser and Light Therapy 2010 Market Report, CAGR from 2010
2014
(4) American Society of Plastic Surgeons
|
9
LipoSonix: New Solution for Fat
Superficial Devices
Noninvasive
Limited to the skin
Require repeat
procedures
Limited body contouring
effects
Minimal discomfort
No downtime
Moderate patient cost
Performed by broad
group of health
practitioners
Surgery/Liposuction
Invasive
Surgery-related risks
Lumpy, asymmetric
results possible
Long recovery period
Long procedures
Can be painful
Downtime
High patient cost
Performed by surgeons
Noninvasive
Effectively destroys targeted fat
tissues
Consistent results across
treatment area
Single, less than one hour
procedure
Little to no downtime
Performed by broad group of
health practitioners |
10
LipoSonix Anticipated Regulatory Clearance Milestones
Q1 2011
Q2 2011
Q3 2011
Q4 2011
Q1 2012
Q2 2012
Q3 2012
Q4 2012
Gen 1 FDA Clearance (cleared)
Gen 2 FDA Clearance (targeting Q1 2012)
Gen 2 EU Clearance (targeting Q4 2011)
Gen 2 Rest of World Clearance (targeting beginning in Q4 2011 through 2012)
FDA
Outside the United States |
11
LipoSonix Gen2 Device
2.7x
larger
treatment
area
-
speeds
treatment
time
Improved ergonomics and ease of use
Lighter handheld transducer system (no reticulating arm)
Touch screen interface
Smaller footprint in the physicians office
Improved serviceability |
12
Proficient and Permanent Reduction in Fat Tissue
Patented HIFU technology creates permanent destruction of targeted fat
tissue
Treats at a depth of 11-16 millimeters, destroying the targeted adipose tissue
without damaging tissue outside of the intended focal zone
The normal healing process transports lipids and debris away from the treated site
within 8 to 12 weeks |
13
Successful Clinical Studies
In clinical trials conducted, subjects, on average, achieved a 2.5 cm waist circumference
reduction, with results typically seen in 8 to 12 weeks
Single blind study evaluated across a diverse setting produced significant results
Superior
to
sham
control
in
reducing
waist
circumference
1
cm
greater
waist
reduction
Mean reduction was equivalent to one dress or pant size
No serious adverse or unanticipated adverse device events
24
week
post
treatment
study
any
reported
pain
was
mostly
mild,
short-lived
in
duration and resolved without incident
Clinical trial results published in July, 2011 by the American Society for Aesthetic Plastic
Surgery in Plastic and Reconstructive Surgery |