Gelesis has demonstrated strong demand
for Plenity, helping over 200,000 people on their weight loss
journeys since launch
Company has filed with FDA to make Plenity
available to Over the Counter (OTC), which should significantly
broaden consumer access and reduce the cost to reach new
members
Gelesis Holdings, Inc. (NYSE: GLS) (“Gelesis” or the “Company”),
the maker of Plenity for weight management, today reported
financial results for the year ended December 31, 2022. Plenity is
a novel orally administered, FDA-cleared weight management therapy
that helps people feel satisfied with smaller portions, so they can
eat less and lose weight, while still enjoying the foods they love.
Plenity is the only FDA-cleared aid for weight management for
people with a BMI as low as 25, up to a BMI of 40, with the largest
addressable market of any prescription weight management approach
on the market today.
This press release features multimedia. View
the full release here:
https://www.businesswire.com/news/home/20230328005292/en/
Plenity is the only FDA-cleared aid for
weight management for people with a BMI as low as 25, up to a BMI
of 40, with the largest addressable market of any prescription
weight management approach on the market today. (Photo:Business
Wire)
“In 2022, we demonstrated that there is significant demand for
an effective, affordable, and well tolerated product like Plenity.
We shared in November that we intend to seek FDA approval to make
Plenity available over the counter, or without a prescription, and
we have begun that process this year. We believe this shift will
significantly broaden consumer access to treatment for the millions
of people looking for a weight management solution while reducing
the amount of capital needed to get to profitability,” said Yishai
Zohar, Gelesis founder and CEO. “There is incredible momentum in
obesity medicine right now. Plenity fills a unique gap in the
market: it is extremely well tolerated, affordable, and fits into
your life by allowing you to continue to eat what you love. Looking
ahead, we believe 2023 will be a pivotal year for the company as we
work to build the long-term potential of Plenity.” The Company has
applied with the FDA to make Plenity available without a
prescription, which the Company believes could be achieved as soon
as the third quarter of 2023.
Key Business Metrics
For the Year Ended December
31,
In $000's
2022
2021
New members acquired
121,500
61,400
Units sold
374,224
170,969
Product revenue, net
$
25,558
$
11,185
Average selling price per unit, net
$
68.30
$
65.42
Gross profit
$
(2,000
)
$
1,202
Gross margin
(8
)%
11
%
Fiscal Year 2022 Results
- Product revenue, net, was $25.6 million in 2022 compared to
$11.2 million in 2021, a 129% increase year-over-year.
- In the second half of 2022, we significantly reduced sales and
marketing activities in order to preserve liquidity and focus on
the switch of Plenity to OTC.
- We acquired 121,500 new members during 2022 compared to 61,400
new members during 2021, a 98% increase year-over-year, and sold
374,000 units in 2022 compared to 174,000 units in 2021, a 115%
increase.
- We achieved significant manufacturing cost savings in Plenity
since validating our first commercial manufacturing line at the end
of 2021, however, we recorded an inventory reserve of $13.3 million
in 2022, which impacted gross margin. Before accounting for the
impact of this inventory reserve, our cost of goods sold was
approximately $38 per unit sold in 2022, compared to an average net
selling price of approximately $68 price per unit sold.
- Net loss was $(55.8) million and Adjusted EBITDA was $(83.3)
million in 2022, compared to net loss of $(93.3) million and
Adjusted EBITDA of $(73.8) million in 2021.
A reconciliation of Adjusted EBITDA, a non-GAAP financial
measure, to net loss, its most comparable financial measure under
generally accepted accounting principles in the United States
(“U.S. GAAP”), is included in the tables accompanying this press
release. See “Non-GAAP Financial Measures” for additional important
information regarding Adjusted EBITDA.
Recent Business Highlights
- Gelesis has filed an initial 510(k) application with the FDA to
change the classification of Plenity from prescription-only to be
available over the counter (“OTC”). An OTC classification would
make Plenity widely available and easily accessible, empowering
individuals struggling with excess weight with an easier path to an
effective, affordable, and trusted weight management product. With
Plenity’s unprecedented safety and efficacy profiles, demonstrated
in over 200,000 patients, the company believes this is the optimal
time to pursue an OTC pathway with the FDA.
- In February 2023, Gelesis completed a private placement of $5.0
million in convertible senior secured notes with an existing top
tier shareholder. The Company may issue an additional $5.0 million
to this shareholder upon mutual acceptance of Gelesis meeting
certain conditions.
Outlook for Fiscal Year 2023
In 2023, Gelesis intends to focus the organization on advancing
the process of changing the classification of Plenity to OTC while
also supporting members who are taking Plenity as a prescription.
In light of the pending change to OTC and the impact it may have on
the Company’s commercial strategy, as well as its current levels of
liquidity, the Company has significantly reduced its internal and
external operating costs, including sales and marketing costs.
The Company has engaged Torreya Capital, LLC, to act as the
Company’s exclusive financial advisor to assist in evaluating
strategic alternatives, including potential financing and
commercial partnerships in various geographies. Torreya Capital,
LLC, a Stifel Company, is a leading boutique investment bank that
provides strategic and financial advice to companies in the
healthcare industry. As part of this process, the Company is
seeking additional financing and/or other strategic transactions.
The Company has not set a timetable for the conclusion of its
review and there can be no assurance that this process will result
in the Company pursuing a transaction or that any transaction, if
pursued, will be completed on attractive terms, if at all. If the
Company is unable to complete a transaction, it may be required to
seek a reorganization, liquidation or other restructuring. The
Company does not expect to comment further or provide an update
concerning developments related to this process unless or until the
Company’s Board of Directors has approved a definitive course of
action or otherwise determined that other disclosure is necessary
or appropriate.
Given these factors, the Company will not be issuing guidance
for fiscal year 2023. A more detailed discussion of Gelesis’
liquidity position and risks related thereto will be set forth in
the Company’s Form 10-K that will be filed with the SEC.
Conference Call and Webcast Information
A pre-recorded webcast discussing these results is available on
the “Events & Presentations” section of the Gelesis Investor
Relations website at https://ir.gelesis.com/. The webcast will also
be archived and available for replay.
About Gelesis
Gelesis Holdings Inc. (NYSE: GLS) (“Gelesis”) is a
consumer-centered biotherapeutics company and the maker of
Plenity®, which is inspired by nature and FDA cleared to aid in
weight management. Our first-of-their-kind non-systemic
superabsorbent hydrogels are made entirely from naturally derived
building blocks. They are inspired by the composition and
mechanical properties of raw vegetables, taken by capsule, and act
locally in the digestive system, so people feel satisfied with
smaller portions. Our portfolio includes Plenity® and potential
therapies in development for patients with Type 2 Diabetes,
Non-alcoholic Fatty Liver Disease (NAFLD)/Non-alcoholic
Steatohepatitis (NASH), and Functional Constipation. For more
information, visit gelesis.com, or connect with us on Twitter
@GelesisInc. Plenity® is indicated to aid weight management in
adults with excess weight or obesity, a Body Mass Index (BMI) of
25–40 kg/m², when used in conjunction with diet and exercise.
Important Safety Information about Plenity
- Patients who are pregnant or are allergic to cellulose, citric
acid, sodium stearyl fumarate, gelatin, or titanium dioxide should
not take Plenity.
- To avoid impact on the absorption of medications:
- For all medications that should be taken with food, take them
after starting a meal.
- For all medications that should be taken without food (on an
empty stomach), continue taking on an empty stomach or as
recommended by your physician.
- The overall incidence of side effects with Plenity was no
different than placebo. The most common side effects were diarrhea,
distended abdomen, infrequent bowel movements, and flatulence.
- Contact a doctor right away if problems occur. If you have a
severe allergic reaction, severe stomach pain, or severe diarrhea,
stop using Plenity until you can speak to your doctor.
Rx Only. For the safe and proper use of Plenity or more
information, talk to a healthcare professional, read the Patient
Instructions for Use, or call 1-844-PLENITY.
Forward-Looking Statements
Certain statements, estimates, targets and projections in this
press release may constitute “forward-looking statements” within
the meaning of the federal securities laws. The words “anticipate,”
“believe,” continue,” “could,” “estimate,” “expect,” “intend,”
“may,” “might,” “plan,” “possible,” “potential,” “predict,”
“project,” “should,” “strive,” “would” and similar expressions may
identify forward-looking statements, but the absence of these words
does not mean that statement is not forward looking.
Forward-looking statements are predictions, projections and other
statements about future events that are based on current
expectations and assumptions and, as a result, are subject to risks
and uncertainties. Forward-looking statements include, but are not
limited to, statements regarding Gelesis’ or its management team’s
expectations, hopes, beliefs, intentions or strategies regarding
the future, including those relating to Gelesis’ expected operating
and financial performance and market opportunities. In addition,
any statements that refer to guidance, projections, forecasts, or
other characterizations of future events or circumstances,
including any underlying assumptions, are forward-looking
statements. Forward-looking statements speak only as of the date
they are made. Readers are cautioned not to put undue reliance on
forward-looking statements, and Gelesis assumes no obligation and
does not intend to update or revise these forward-looking
statements, whether as a result of new information, future events,
or otherwise. Gelesis gives no assurance that any expectations set
forth in this press release will be achieved. Various risks and
uncertainties (some of which are beyond Gelesis’ control) or other
factors could cause actual future results, performance or events to
differ materially from those described herein. For a description of
such factors, please see the section entitled "Risk Factors" in
Gelesis’ most recent Annual Report on Form 10-K and in other
filings that Gelesis makes with the Securities and Exchange
Commission. These filings address important risks and uncertainties
that could cause actual results and events to differ materially
from those contained in the forward-looking statements.
Disclaimer
Gelesis assumes no obligation and does not intend to update or
revise the results provided in this press release. The results
provided in this press release represent past performance and are
not necessarily predictive of future results.
Plans to Make Plenity Available Without a
Prescription
We believe Plenity’s advantages are its differentiated
safety-to-efficacy profile, broad approved labeling, and
affordability to the consumer. Accordingly, we believe it is
important that Plenity be widely available and easily accessible to
consumers. We are pursuing an application with the FDA to change
Plenity's classification in the United States from
prescription-only to over-the-counter. In addition to making
Plenity more accessible to people struggling with excess weight, we
believe making Plenity available over-the-counter could reduce
costs associated with acquiring new members and allow us to reduce
costs associated with the prescription granting process, while also
enabling new sales channels for the Company.
Key Business Metrics
We monitor the following key metrics to help us evaluate our
business, identify trends affecting our business, formulate
business plans and make strategic decisions. We believe the
following metrics are useful in evaluating our business:
New members acquired
We define new members acquired as the number of consumers in the
United States who have begun their weight loss journey with Plenity
during the financial period presented. This is the total number of
recurring and non-recurring consumers who have begun their weight
loss journey during the financial period presented. We do not
differentiate from recurring and non-recurring consumers as of this
date as (i) we strongly believe every member’s weight-loss journey
is chronic and long-term in nature, and (ii) we have not initiated
our long-term strategy and mechanisms to retain and/or win-back
members. We will continue to evaluate the utility of this business
metric in future periods.
Units sold
Units sold is defined as the number of 28-day supply units of
Plenity sold through strategic partnerships with online pharmacies
and telehealth providers as well as the units sold to our strategic
partners outside the United States. Note that the terms “units” and
“monthly kits”, as mentioned in Gelesis’ various public disclosures
and filings, are synonymous when used to describe the sales volume
of Plenity.
Product revenue, net
We recognize product revenue in accordance with Accounting
Standards Codification Topic 606, Revenue from Contracts with
Customers, when we transfer promised goods or services to customers
in an amount that reflects the consideration to which the entity
expects to be entitled in exchange for those goods or services.
Our product revenue is derived from product sales of Plenity,
net of estimates of variable consideration for which reserves are
established for expected product returns, shipping charges to
end-users, pharmacy dispensing and platform fees, merchant and
processing fees, and promotional discounts offered to
end-users.
Average selling price per unit, net
Average selling price per unit, net is the gross price per unit
sold during the period net of estimates of per unit variable
consideration for which reserves are established for expected
product returns, shipping charges to end-users, pharmacy dispensing
and platform fees, merchant and processing fees, and promotional
discounts offered to end-users.
Gross profit and gross margin
Our gross profit represents product revenue, net, less our total
cost of goods sold, and our gross margin is our gross profit
expressed as a percentage of our product revenue, net. Our gross
profit and gross margin have been and will continue to be affected
by a number of factors, including the prices we charge for our
product, the costs we incur from our vendors for certain components
of our cost of goods sold, the mix of channel sales in a period,
and our ability to sell our inventory.
Non-GAAP Financial Measures
In addition to our financial results determined in accordance
with GAAP, we believe that Adjusted EBITDA, a non-GAAP measure, is
useful in evaluating our operating performance. We define “Adjusted
EBITDA” as net (loss) income before depreciation and amortization
expenses, provision for (benefit from) income taxes, interest
expense, net, stock-based compensation and (gains) and losses
related to changes in fair value of our warrant liability, our
convertible promissory note liability, our tranche rights
liability, our earnout liability and the One S.r.l. call option. We
use Adjusted EBITDA to evaluate our ongoing operations and for
internal planning and forecasting purposes because it facilitates
internal comparisons of our historical operating performance. We
believe that this non-GAAP financial measure, when taken together
with the corresponding GAAP financial measure, net loss, provides
meaningful supplemental information regarding our performance by
excluding certain items that may not be indicative of our business,
results of operations, or outlook. We consider Adjusted EBITDA to
be an important measure because it helps illustrate underlying
trends in our business and our historical operating performance on
a more consistent basis. We believe that Adjusted EBITDA is helpful
to our investors as it is a metric used by management in assessing
the health of our business and our operating performance.
However, non-GAAP financial information is presented for
supplemental informational purposes only, has limitations as an
analytical tool and should not be considered in isolation or as a
substitute for financial information presented in accordance with
GAAP. In addition, other companies, including companies in our
industry, may calculate similarly titled non-GAAP financial
measures differently or may use other measures to evaluate their
performance, all of which could reduce the usefulness of Adjusted
EBITDA as a tool for comparison. A reconciliation is provided below
for Adjusted EBITDA to the most directly comparable financial
measure stated in accordance with GAAP. Investors are encouraged to
review the related GAAP financial measure and the reconciliation of
this non-GAAP financial measure to its most directly comparable
GAAP financial measure, and not to rely on any single financial
measure to evaluate our business.
SELECTED CONDENSED
CONSOLIDATED BALANCE SHEETS
(In thousands,
Unaudited)
December 31,
December 31,
2022
2021
ASSETS
Cash and cash equivalents
$
7,412
$
28,397
Accounts receivable and grants
receivable
4,592
9,903
Inventories
6,865
13,503
Property and equipment, net
59,335
58,515
All other current and non-current
assets
25,120
35,983
Total assets
$
103,324
$
146,301
LIABILITIES, REDEEMABLE
CONVERTIBLE PREFERRED STOCK AND STOCKHOLDERS’ EQUITY
(DEFICIT)
Accounts payable
$
4,131
$
10,066
Accrued expenses and other current
liabilities
10,468
13,660
Deferred income, current portion
27,793
32,370
Notes payable and convertible promissory
notes, current portion
35,357
29,078
Warrant liabilities
130
15,821
Earnout liability
563
—
Deferred income, non-current portion
9,544
8,914
Notes payable, non-current portion
25,342
35,131
All other current and non-current
liabilities
2,462
7,648
Total liabilities
115,790
152,688
Noncontrolling interest
12,590
11,855
Redeemable convertible preferred stock
—
311,594
Total stockholders’ deficit
(25,056
)
(329,836
)
Total liabilities, noncontrolling
interest, redeemable convertible preferred stock and stockholders’
deficit
$
103,324
$
146,301
CONDENSED CONSOLIDATED
STATEMENTS OF OPERATIONS
(In thousands,
Unaudited)
For the Year Ended December
31,
2022
2021
Revenue:
Product revenue, net
$
25,558
$
11,185
Licensing revenue
209
—
Total revenue, net
25,767
11,185
Operating expenses:
Costs of goods sold
27,558
9,983
Selling, general and administrative
99,135
71,041
Research and development
18,613
12,867
Amortization of intangible assets
2,267
2,267
Total operating expenses
147,573
96,158
Loss from operations
(121,806
)
(84,973
)
Change in the fair value of earnout
liability
58,308
—
Change in the fair value of convertible
promissory notes
(2,559
)
(128
)
Change in the fair value of warrants
7,084
(7,646
)
Interest expense, net
(991
)
(1,364
)
Other income, net
4,664
781
Loss before income taxes
(55,300
)
(93,330
)
Provision for income taxes
480
17
Net loss
(55,780
)
(93,347
)
Accretion of Legacy Gelesis senior
preferred stock to redemption value
(37,934
)
(94,134
)
Accretion of noncontrolling interest put
option to redemption value
(253
)
(376
)
Income allocated to noncontrolling
interest holder
(1,095
)
-
Net loss attributable to common
stockholders
$
(95,062
)
$
(187,857
)
Net loss per share attributable to common
stockholders—basic and diluted
$
(1.35
)
$
(32.89
)
Weighted average common shares
outstanding—basic and diluted
70,300,772
5,712,042
CONDENSED CONSOLIDATED
STATEMENTS OF CASH FLOWS
(In thousands,
Unaudited)
For the Year Ended December
31,
2022
2021
Cash flows from operating
activities:
Net loss
$
(55,780
)
$
(93,347
)
Adjustments to reconcile net loss to net
cash used in operating activities:
Amortization of intangible assets
2,267
2,267
Increase in inventory reserves
13,334
—
Reduction in carrying amount of
right-of-use assets
475
449
Depreciation
3,221
1,524
Stock-based compensation
29,777
5,532
Issuance of common stock commitment
shares
500
—
Gain on sales of common stock
(1
)
—
Unrealized loss on foreign currency
transactions
608
(37
)
Non-cash interest expense
215
173
Gain on CMS amendment
(209
)
—
Loss on One S.r.l. amendment
278
—
Accretion on marketable securities
—
(1
)
Change in the fair value of earnout
liability
(58,308
)
—
Change in the fair value of warrants
(7,084
)
7,646
Change in the fair value of convertible
promissory notes
2,559
128
Change in fair value of One S.r.l. call
option
(1,462
)
1,024
Change in fair value of interest rate swap
contract
(856
)
146
Changes in operating assets and
liabilities:
—
—
Account receivables
(1,536
)
70
Grants receivable
5,216
(1,723
)
Prepaid expenses and other current
assets
7,181
(8,029
)
Inventories
(6,249
)
(8,645
)
Other assets
(449
)
107
Accounts payable
(5,415
)
2,604
Accrued expenses and other current
liabilities
(269
)
8,709
Operating lease liabilities
(474
)
(440
)
Deferred income
(3,395
)
33,140
Other long-term liabilities
(1,872
)
(6,588
)
Net cash used in operating activities
(77,728
)
(55,291
)
Cash flows from investing
activities:
Purchases of property and equipment
(9,120
)
(19,917
)
Maturities of marketable securities
—
24,000
Net cash (used in) provided by investing
activities
(9,120
)
4,083
Cash flows from financing
activities:
Proceeds from Business Combination, net of
transaction costs
70,479
—
Principal repayment of notes payable
(2,033
)
(302
)
Repayment of convertible promissory
notes
(27,284
)
—
Proceeds from convertible promissory
notes
25,000
27,000
Proceeds from issuance of promissory notes
(net of issuance costs of $0 and $207, respectively)
—
5,679
Proceeds from exercise of warrants
4
10
Proceeds from exercise of share-based
awards
120
146
Proceeds from sales of common stock, net
of issuance costs
39
—
Net cash provided by financing
activities
66,325
32,533
Effect of exchange rates on cash
(462
)
(1,072
)
Net decrease in cash
(20,985
)
(19,747
)
Cash and cash equivalents at beginning of
year
28,397
48,144
Cash and cash equivalents at end of
period
$
7,412
$
28,397
NET LOSS TO ADJUSTED EBITDA
RECONCILIATION
(In thousands, Unaudited)
For the Year Ended December
31,
2022
2021
In thousands
Adjusted EBITDA
Net loss
$
(55,780
)
$
(93,347
)
Provision for income taxes
480
17
Depreciation and amortization
5,488
3,791
Stock based compensation expense
29,777
5,532
Change in fair value of earnout
liability
(58,308
)
—
Change in fair value of warrants
(7,084
)
7,646
Change in fair value of convertible
promissory notes
2,559
128
Change in fair value of One S.r.l. call
option
(1,462
)
1,024
Interest expense, net
991
1,364
Adjusted EBITDA
$
(83,339
)
$
(73,845
)
View source
version on businesswire.com: https://www.businesswire.com/news/home/20230328005292/en/
Investors & Media: ir@gelesis.com
Gelesis (NYSE:GLS)
Graphique Historique de l'Action
De Déc 2024 à Jan 2025
Gelesis (NYSE:GLS)
Graphique Historique de l'Action
De Jan 2024 à Jan 2025