Miravo Healthcare™ Announces Third Quarter 2021 Results
Miravo Healthcare reported Q3 2021 adjusted total revenue of $17.1 million, a 3% increase year-over-year, while adjusted EBITDA rose 7% to $7.0 million. Prescription growth for key products Blexten and Cambia was strong, with increases of 16% and 5% respectively. However, total revenue for the nine months decreased by 4% to $51.6 million, alongside a 15% drop in adjusted EBITDA. The company made notable strides with the launch of Resultz in the U.S. and expanded its product lineup with pediatric use approval for Blexten.
- Adjusted total revenue increased by 3% to $17.1 million for Q3 2021.
- Adjusted EBITDA rose by 7% to $7.0 million for Q3 2021.
- Revenue from Blexten, Cambia, and Suvexx increased by 24% to $8.1 million.
- Blexten prescriptions up by 16% and Cambia prescriptions up by 5% year-over-year.
- Successful launch of Resultz in the U.S. market.
- Total adjusted revenue for the nine months decreased by 4% to $51.6 million.
- Adjusted EBITDA decreased by 15% to $18.8 million for the nine months.
- Impairment loss of $14.7 million on goodwill and intangible assets due to COVID-19 impact.
- Q3 2021 Adjusted Total Revenue -
- Q3 2021 Adjusted EBITDA -
- Blexten Canadian Prescriptions Increased
- Cambia Canadian Prescriptions Increased
Miravo to Host Conference Call/Audio Webcast
Key Developments
Three months ended
-
Adjusted total revenue(1) was
, an increase of$17.1 million 3% compared to for the three months ended$16.7 million September 30, 2020 . -
Adjusted EBITDA(1) was
, an increase of$7.0 million 7% compared to for the three months ended$6.6 million September 30, 2020 . -
Revenue related to Blexten®, Cambia® and Suvexx® was
, an increase of$8.1 million 24% compared to revenue of for the three months ended$6.5 million September 30, 2020 . Total Canadian prescriptions of Blexten and Cambia increased by16% and5% respectively compared to the three months endedSeptember 30, 2020 . -
The Company repaid
($3.7 million US ) of the Amortization Loan to$2.9 million Deerfield Management Company, L.P. (Deerfield). -
As at
September 30, 2021 , cash and cash equivalents were .$28.4 million
Nine months ended
-
Adjusted total revenue(1) was
, a decrease of$51.6 million 4% compared to for the nine months ended$53.6 million September 30, 2020 . -
Adjusted EBITDA(1) was
, a decrease of$18.8 million 15% compared to for the nine months ended$22.2 million September 30, 2020 . -
Revenue related to Blexten, Cambia and Suvexx was
, an increase of$23.5 million 26% compared to revenue of for the nine months ended$18.7 million September 30, 2020 . Canadian prescriptions of Blexten and Cambia increased by22% and10% respectively compared to the nine months endedSeptember 30, 2020 . -
The Company repaid
($10.3 million US ) of the Amortization Loan to Deerfield.$8.3 million
(1) Non-International Financial Reporting Standards (IFRS) financial measure defined by the Company below.
Business Update
-
In
October 2021 , Resultz was commercially launched in the U.S. market byThe Mentholatum Company , Resultz is marketed in theU.S. under the brand name Mentholatum Kids Headlice Removal Kit. The Company’s Irish subsidiary,Nuvo Pharmaceuticals (Ireland ) DAC (Miravo Ireland) receives revenue from the supply of finished product toThe Mentholatum Company . -
In
September 2021 , Miravo Ireland’s distribution partner for Suvexx inSouth Korea , SK Chemicals Co., Ltd. (SK Chemicals), filed the Suvexx marketing authorization application with theMinistry of Food and Drug Safety (the MFDS) inSouth Korea . InJuly 2021 , Miravo Ireland entered into an exclusive license and supply agreement with SK Chemicals for the exclusive right to commercialize Suvexx in theRepublic of South Korea . Miravo Ireland will receive up to€1.1 million in upfront consideration, regulatory and sales-based milestone payments, as well as royalties on net sales of Suvexx inSouth Korea and revenue pursuant to the supply of product. -
In
August 2021 , Miravo announcedHealth Canada issued a Notice of Compliance (NOC) in relation to the Company’s Supplement to New Drug Submission for the pediatric use of Blexten. The pediatric use expands the label for use in children as young as 4 years old and includes the two new dosage formats; a 2.5mg/mL oral solution and a 10mg Quick Melt tablet. Upon commercial launch, which is anticipated for Q1 2022, the pediatric formats will be available to patients with a prescription from their healthcare provider.
"We are encouraged by the strength of our key promoted brands, Blexten, Cambia and Suvexx, which continued their year-over-year gains in prescription and revenue growth despite the fact that many prescribers have not yet resumed seeing patients in-person at pre-COVID-19 pandemic levels. We anticipate that the gradual return of in-person, patient-physician visits, over the coming quarters, will provide enhanced opportunities for patient education and new prescription growth,” said
Third Quarter 2021 Financial Results
Adjusted total revenue was
Revenue attributable to the Commercial Business segment increased during the three months ended
The Production and Service Business segment revenue decreased during the three months ended
The increase in revenue attributable to the License and Royalty business segment during the three months ended
Adjusted EBITDA was
Non-IFRS Financial Measures
The Company discloses non-IFRS measures (such as adjusted total revenue, adjusted EBITDA, adjusted EBITDA per share and cash value of loans) that do not have standardized meanings prescribed by IFRS. The Company believes that shareholders, investment analysts and other readers find such measures helpful in understanding the Company’s financial performance. Non-IFRS financial measures do not have any standardized meaning prescribed by IFRS and may not have been calculated in the same way as similarly named financial measures presented by other companies. These measures should be considered as supplemental in nature and not as a substitute for related financial information prepared in accordance with IFRS. Please see below and refer to the MD&A for a reconciliation of these measures to standardized IFRS measures.
Adjusted Total Revenue
The Company defines adjusted total revenue as total revenue, plus amounts billed to customers for existing contract assets, less revenue recognized upon recognition of a contract asset. Management believes adjusted total revenue is a useful supplemental measure to determine the Company’s ability to generate cash from its customer contracts used to fund its operations.
The following is a summary of how adjusted total revenue is calculated:
|
Three months ended
|
Nine months ended
|
||||||
|
2021 |
2020 |
2021 |
2020 |
||||
in thousands |
$ |
$ |
$ |
$ |
||||
Total revenue |
16,989 |
16,601 |
51,198 |
56,492 |
||||
Add: |
||||||||
Amounts billed to customers for existing contract assets |
141 |
68 |
381 |
2,632 |
||||
Deduct: |
|
|
|
|
||||
Revenue recognized upon recognition of a contract asset |
- |
- |
- |
(5,496) |
||||
Adjusted total revenue |
17,130 |
16,669 |
51,579 |
53,628 |
Adjusted EBITDA
EBITDA refers to net income (loss) determined in accordance with IFRS, before depreciation and amortization, net interest expense (income) and income tax expense (recovery). The Company defines adjusted EBITDA as EBITDA, plus amounts billed to customers for existing contract assets, inventory step-up expenses, stock-based compensation expense, Other Expenses (Income), less revenue recognized upon recognition of a contract asset and other income. Management believes adjusted EBITDA is a useful supplemental measure to determine the Company’s ability to generate cash available for working capital, capital expenditures, debt repayments, interest expense and income taxes.
The following is a summary of how EBITDA and adjusted EBITDA are calculated:
|
Three Months ended
|
Nine Months ended
|
||||||
|
2021 |
2020 |
2021 |
2020 |
||||
|
$ |
$ |
$ |
$ |
||||
Net income (loss) |
(17,770) |
(2,832) |
(26,612) |
(6,528) |
||||
Add back: |
|
|
|
|
||||
Income tax expense (1) |
811 |
(7) |
2,384 |
1,587 |
||||
Net interest expense |
2,512 |
2,904 |
7,577 |
9,019 |
||||
Depreciation and amortization |
2,021 |
2,250 |
6,125 |
6,965 |
||||
EBITDA |
(12,426) |
2,315 |
(10,526) |
11,043 |
||||
Add back: |
|
|
|
|
||||
Amounts billed to customers for existing contract assets |
141 |
68 |
381 |
2,632 |
||||
Stock-based compensation |
71 |
50 |
311 |
208 |
||||
Deduct: |
|
|
|
|
||||
Revenue recognized upon recognition of a contract asset |
- |
- |
- |
(5,496) |
||||
Other Expenses (Income): |
|
|
|
|
||||
Change in fair value of derivative liabilities (2) |
2,929 |
5,240 |
14,447 |
11,141 |
||||
Change in fair value of contingent and variable consideration |
94 |
(289) |
(1,005) |
1,586 |
||||
Impairment (3) |
14,682 |
- |
14,682 |
- |
||||
Foreign currency loss (gain) |
1,439 |
(1,146) |
162 |
1,441 |
||||
Inventory step-up |
- |
358 |
35 |
1,059 |
||||
Other losses (gains) |
110 |
(31) |
284 |
(1,413) |
||||
Adjusted EBITDA |
7,040 |
6,565 |
18,771 |
22,201 |
(1) Income tax expense for the three and nine months ended
(2) The Company’s derivative liabilities are measured at fair value through profit or loss at each reporting date. As a result of the increase in the share price in the current quarter and an increase in the volatility of the Company’s shares, amongst other inputs, the value of the Company’s derivative liabilities increased and the Company recognized losses of
(3) During the three and nine months ended
With respect to the above noted impairment, the Company will continue to carefully monitor the situation as it pertains to COVID-19. With the ongoing prevalence of the COVID-19 pandemic, the length and severity of impacts on the Company’s business and industry in which it operates remain subject to uncertainty, and accordingly, may materially and adversely affect our commercial expectations and the assumptions used in our consideration of the impairment of goodwill and intangible assets. See “Impairment” and “Risk Factors” in the MD&A.
Management to Host Conference Call/Webcast
Management will host a conference call to discuss the results today (
A live audio webcast and replay webcast of the conference call will be available through https://onlinexperiences.com/Launch/QReg/ShowUUID=1E07F0A9-7B64-4D3F-9EAA-D9A1C0CE92B9
Please connect at least 15 minutes prior to the conference call to ensure adequate time for any software download that may be required to hear the webcast.
About
Miravo is a Canadian focused, healthcare company with global reach and a diversified portfolio of commercial products. The Company’s products target several therapeutic areas, including pain, allergy, neurology and dermatology. The Company’s strategy is to in-license and acquire growth-oriented, complementary products for Canadian and international markets. Miravo’s head office is located in
Forward-Looking Statements
This press release contains “forward-looking information” as defined under Canadian securities laws (collectively, “forward-looking statements”). The words “plans”, “expects”, “does not expect”, “goals”, “seek”, “strategy”, “future”, “estimates”, “intends”, “anticipates”, “does not anticipate”, “projected”, “believes” or variations of such words and phrases or statements to the effect that certain actions, events or results “may”, “will”, “could”, “would”, “should”, “might”, “likely”, “occur”, “be achieved” or “continue” and similar expressions identify forward-looking statements. In addition, any statements that refer to expectations, intentions, projections or other characterizations of future events or circumstances contain forward-looking statements. These forward-looking statements include statements regarding anticipated product launches, responses to COVID-19, milestone payments, royalties and license approvals.
Forward-looking statements are not historical facts but instead represent management’s expectations, estimates and projections regarding future events or circumstances, including the anticipated receipt of certain milestone and royalty payments, the anticipated launch of certain products and approvals therefor, and the potential impact of COVID-19. Such forward-looking statements are qualified in their entirety by the inherent risks, uncertainties and changes in circumstances surrounding future expectations which are difficult to predict and many of which are beyond the control of the Company. Forward-looking statements are necessarily based on a number of estimates and assumptions that, while considered reasonable by management of the Company as of the date of this press release, are inherently subject to significant business, economic and competitive uncertainties and contingencies and may prove to be incorrect. Material factors and assumptions used to develop the forward-looking statements, and material risk factors that could cause actual results to differ materially from the forward-looking statements, include but are not limited to, the denial of regulatory approvals, the delay or failure to meet anticipated product launches, the failure to meet certain milestones or collect certain royalties, the potential impact of COVID-19 on the Company’s operations, business and financial results and other factors, many of which are beyond the control of the Company. Additional factors that could cause the Company’s actual results and financial condition to differ materially from those indicated in the forward-looking statements include, among others, the risk factors included in the Company’s most recent Annual Information Form dated
All forward-looking statements are based only on information currently available to the Company and are made as of the date of this press release. Except as expressly required by applicable Canadian securities law, the Company assumes no obligation to publicly update or revise any forward-looking statement, whether as a result of new information, future events or otherwise. All forward-looking statements in this press release are qualified by these cautionary statements.
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Investor Relations
905 326 1888 ext 60
stefan@bristolir.com
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