Vertex Reports First-Quarter 2020 Financial Results
-Product revenues of
-Company raises revenue guidance; now expects 2020 CF revenues of
"The COVID-19 pandemic has presented unprecedented challenges to societies, communities and businesses around the world, and while these global challenges will continue for some time to come, I am very proud of how
First-Quarter 2020 Financial Highlights
|
Three Months Ended |
|
% |
||||||||
|
2020 |
|
2019 |
|
Change |
||||||
|
(in millions, except per share amounts) |
||||||||||
Product revenues, net |
$ |
1,515 |
|
|
|
$ |
857 |
|
|
|
77% |
TRIKAFTA |
$ |
895 |
|
|
|
$ |
— |
|
|
|
|
SYMDEKO/SYMKEVI |
$ |
173 |
|
|
|
$ |
320 |
|
|
|
|
ORKAMBI |
$ |
234 |
|
|
|
$ |
293 |
|
|
|
|
KALYDECO |
$ |
213 |
|
|
|
$ |
244 |
|
|
|
|
|
|
|
|
|
|
|
|
|
|
||
GAAP Operating income |
$ |
720 |
|
|
|
$ |
277 |
|
|
|
160% |
Non-GAAP Operating income |
$ |
877 |
|
|
|
$ |
377 |
|
|
|
133% |
|
|
|
|
|
|
|
|
|
|
||
GAAP Net income |
$ |
603 |
|
|
|
$ |
269 |
|
|
|
124% |
Non-GAAP Net income |
$ |
674 |
|
|
|
$ |
296 |
|
|
|
128% |
|
|
|
|
|
|
|
|
|
|
||
GAAP Net income per share - diluted |
$ |
2.29 |
|
|
|
$ |
1.03 |
|
|
|
122% |
Non-GAAP Net income per share - diluted |
$ |
2.56 |
|
|
|
$ |
1.14 |
|
|
|
125% |
Total product revenues increased 77% compared to the first quarter of 2019, primarily driven by the uptake of TRIKAFTA in the
GAAP and Non-GAAP net income each increased more than 120% compared to the first quarter of 2019, largely driven by the strong growth in total product revenues.
Cash, cash equivalents and marketable securities as of
First-Quarter 2020 Expenses
|
Three Months Ended |
||||||||
|
2020 |
|
2019 |
||||||
|
(in millions) |
||||||||
Combined GAAP R&D and SG&A expenses |
$ |
631 |
|
|
|
$ |
487 |
|
|
Combined Non-GAAP R&D and SG&A expenses |
$ |
477 |
|
|
|
$ |
388 |
|
|
|
|
|
|
|
|
|
|
||
GAAP R&D expense |
$ |
449 |
|
|
|
$ |
339 |
|
|
Non-GAAP R&D expense |
$ |
337 |
|
|
|
$ |
273 |
|
|
|
|
|
|
|
|
|
|
||
GAAP SG&A expense |
$ |
182 |
|
|
|
$ |
147 |
|
|
Non-GAAP SG&A expense |
$ |
140 |
|
|
|
$ |
114 |
|
|
|
|
|
|
|
|
|
|
||
GAAP income taxes |
$ |
55 |
|
|
|
$ |
52 |
|
|
Non-GAAP income taxes |
$ |
184 |
|
|
|
$ |
81 |
|
|
|
|
|
|
|
|
|
|
||
GAAP effective tax rate |
|
8 |
|
% |
|
|
16 |
|
% |
Non-GAAP effective tax rate |
|
21 |
|
% |
|
|
21 |
|
% |
Combined GAAP and Non-GAAP R&D and SG&A expenses increased compared to the first quarter of 2019, primarily due to the incremental investment to support the global use of
GAAP and Non-GAAP income taxes increased compared to the first quarter of 2019 primarily due to
Full-Year 2020 Financial Guidance
|
|
Current FY 2020 |
Previous FY 2020 |
|
||
|
|
|
|
|
|
|
TOTAL product revenues |
$ |
5.3 to 5.6 billion |
$ |
5.1 to 5.3 billion |
|
|
|
|
|
|
|
|
|
Combined GAAP R&D and SG&A expenses |
|
Unchanged |
$ |
2.4 to 2.55 billion |
|
|
Combined Non-GAAP R&D and SG&A expenses |
|
Unchanged |
$ |
1.95 to 2.0 billion |
|
|
Non-GAAP effective tax rate |
Unchanged |
21% to 22% |
Key Business Highlights:
Approved Medicines:
Supply Chain for Approved CF Medicines
- The global COVID-19 outbreak has not had any impact on the continuity of Vertex’s supply chain for its approved medicines.
-
Vertex remains highly confident in its ability to continue to supply all of its approved medicines to patients around the world.
TRIKAFTA (elexacaftor, tezacaftor and ivacaftor)
-
Vertex has seen rapid uptake of TRIKAFTA across all groups of eligible patients following approval of this medicine by theU.S. Food and Drug Administration (FDA) inOctober 2019 . The majority of the approximately 18,000 eligible patients have now initiated treatment with TRIKAFTA. -
In
Europe , the Marketing Authorization Application for the elexacaftor, tezacaftor and ivacaftor triple combination in patients with at least one F508del mutation ages 12 and older continues to be under review with theEuropean Medicines Agency (EMA). -
Vertex also recently submitted applications for approval of the elexacaftor, tezacaftor and ivacaftor triple combination for patients with at least one F508del mutation ages 12 and older inAustralia andSwitzerland . -
Vertex recently completed enrollment for a Phase 3 study evaluating the use of the elexacaftor, tezacaftor and ivacaftor triple combination regimen in children with CF ages 6 through 11 who have two copies of the F508del mutation or who have one F508del mutation and one minimal function mutation. Pending data from the study,Vertex plans to submit a supplemental New Drug Application (sNDA) to theU.S. FDA in the second half of 2020 for children ages 6-11 with at least one F508del mutation, followed by regulatory submissions in other countries.
KALYDECO (ivacaftor)
-
Vertex recently completed the submission of an sNDA to theU.S. FDA and Type 2 variation to the EMA for the use of KALYDECO in infants ages four to less than six months. KALYDECO is currently approved for use in infants as young as six months of age in both geographies.
Development Pipeline:
Alpha-1 Antitrypsin (AAT) Deficiency:
-
Vertex has temporarily paused screening and enrollment in the Phase 2 study of VX-814; however, the study remains active andVertex continues to initiate new clinical trial sites to enable future patient enrollment.
Beta Thalassemia and Sickle Cell Disease
-
Vertex and its partner CRISPR Therapeutics remain on track to provide additional data from the two ongoing Phase 1/2 studies of the investigational CRISPR/Cas9 gene-editing therapy CTX001 in patients with transfusion-dependent beta thalassemia and in patients with severe sickle cell disease in 2020. New data expected in 2020 include initial data from additional patients dosed in each of the Phase 1/2 studies and longer duration follow-up data for the first patients dosed in each study. Screening, enrollment and mobilization in these studies is ongoing; however, no additional patients are scheduled to initiate conditioning or dosing at this time.
Focal Segmental Glomerulosclerosis (FSGS):
-
Vertex recently initiated a Phase 2 proof-of-concept study of VX-147 in people with FSGS. - The 13-week open-label Phase 2 study is designed to evaluate the reduction in proteinuria in people with FSGS after treatment with VX-147.
Type 1 Diabetes:
-
Vertex continues to advance its cell therapy program for the treatment of type 1 diabetes and expects to initiate clinical development in patients in late 2020 or early 2021.
Investments in External Innovation
-
Expanding Capabilities in Genetic Therapies: In April,
Vertex entered into a collaboration with Affinia Therapeutics to gain access to a novel library of AAV capsids that will bolsterVertex 's ongoing research and development work in genetic therapies. The goal of the collaboration will be to develop genetic therapies for people affected by Duchenne muscular dystrophy (DMD), myotonic dystrophy 1 (DM1) and CF. -
mRNA Therapies for CF: Based on promising preclinical data generated to date,
Vertex and Moderna recently extended their research collaboration aimed at the discovery and development of mRNA therapeutics for the treatment of CF.
Non-GAAP Financial Measures
In this press release,
First-Quarter Results Consolidated Statements of Operations (in thousands, except per share amounts) (unaudited) |
||||||||
|
Three Months Ended |
|||||||
|
2020 |
|
2019 |
|||||
Revenues: |
|
|
|
|||||
Product revenues, net |
$ |
1,515,107 |
|
|
$ |
857,253 |
|
|
Collaboration and royalty revenues |
— |
|
|
1,182 |
|
|||
Total revenues |
1,515,107 |
|
|
858,435 |
|
|||
Costs and expenses: |
|
|
|
|||||
Cost of sales |
162,497 |
|
|
95,092 |
|
|||
Research and development expenses |
448,528 |
|
|
339,490 |
|
|||
Sales, general and administrative expenses |
182,258 |
|
|
147,045 |
|
|||
Change in fair value of contingent consideration |
1,600 |
|
|
— |
|
|||
Total costs and expenses |
794,883 |
|
|
581,627 |
|
|||
Income from operations |
720,224 |
|
|
276,808 |
|
|||
Interest income |
12,576 |
|
|
15,615 |
|
|||
Interest expense |
(14,136 |
) |
|
(14,868 |
) |
|||
Other (expense) income, net (1) |
(61,130 |
) |
|
42,610 |
|
|||
Income before provision for income taxes |
657,534 |
|
|
320,165 |
|
|||
Provision for income taxes |
54,781 |
|
|
51,534 |
|
|||
Net income |
$ |
602,753 |
|
|
$ |
268,631 |
|
|
|
|
|
|
|||||
Net income per common share: |
|
|
|
|||||
Basic |
$ |
2.32 |
|
|
$ |
1.05 |
|
|
Diluted |
$ |
2.29 |
|
|
$ |
1.03 |
|
|
Shares used in per share calculations: |
|
|
|
|||||
Basic |
259,815 |
|
|
255,695 |
|
|||
Diluted |
263,515 |
260,175 |
Reconciliation of GAAP to Non-GAAP Net Income First-Quarter Results (in thousands, except per share amounts) (unaudited) |
||||||||
|
Three Months Ended |
|||||||
|
2020 |
|
2019 |
|||||
GAAP net income |
$ |
602,753 |
|
|
$ |
268,631 |
|
|
Stock-based compensation expense |
115,706 |
|
|
93,791 |
|
|||
Decrease (increase) in fair value of strategic investments (1) |
44,870 |
|
|
(43,551 |
) |
|||
Increase in fair value of contingent consideration (2) |
1,600 |
|
|
— |
|
|||
Collaborative revenues and expenses (3) |
36,250 |
|
|
6,351 |
|
|||
Acquisition-related costs (4) |
2,883 |
|
|
— |
|
|||
Total non-GAAP adjustments to pre-tax income |
201,309 |
|
|
56,591 |
|
|||
Tax adjustments (5) |
(129,608 |
) |
|
(29,392 |
) |
|||
Non-GAAP net income |
$ |
674,454 |
|
|
$ |
295,830 |
|
|
|
|
|
|
|||||
Net income per diluted common share: |
|
|
|
|||||
GAAP |
$ |
2.29 |
|
|
$ |
1.03 |
|
|
Non-GAAP |
$ |
2.56 |
|
|
$ |
1.14 |
|
|
Shares used in diluted per share calculations: |
|
|
|
|||||
GAAP and Non-GAAP |
263,515 |
|
|
260,175 |
|
Reconciliation of GAAP to Non-GAAP Revenues and Expenses First-Quarter Results (in thousands) (unaudited) |
||||||||
|
Three Months Ended |
|||||||
|
2020 |
|
2019 |
|||||
GAAP total revenues |
$ |
1,515,107 |
|
|
$ |
858,435 |
|
|
Collaborative revenues |
— |
|
|
(141 |
) |
|||
Non-GAAP total revenues |
$ |
1,515,107 |
|
|
$ |
858,294 |
|
|
|
|
|
|
|||||
|
Three Months Ended |
|||||||
|
2020 |
|
2019 |
|||||
GAAP cost of sales |
$ |
162,497 |
|
|
$ |
95,092 |
|
|
Stock-based compensation expense |
(1,361 |
) |
|
(1,338 |
) |
|||
Non-GAAP cost of sales |
$ |
161,136 |
|
|
$ |
93,754 |
|
|
|
|
|
|
|||||
GAAP research and development expenses |
$ |
448,528 |
|
|
$ |
339,490 |
|
|
Stock-based compensation expense |
(72,687 |
) |
|
(59,715 |
) |
|||
Collaborative expenses (3) |
(36,250 |
) |
|
(6,492 |
) |
|||
Acquisition-related costs (4) |
(2,678 |
) |
|
— |
|
|||
Non-GAAP research and development expenses |
$ |
336,913 |
|
|
$ |
273,283 |
|
|
|
|
|
|
|||||
GAAP sales, general and administrative expenses |
$ |
182,258 |
|
|
$ |
147,045 |
|
|
Stock-based compensation expense |
(41,658 |
) |
|
(32,738 |
) |
|||
Acquisition-related costs (4) |
(205 |
) |
|
— |
|
|||
Non-GAAP sales, general and administrative expenses |
$ |
140,395 |
|
|
$ |
114,307 |
|
|
|
|
|
|
|||||
Combined non-GAAP R&D and SG&A expenses |
$ |
477,308 |
|
|
$ |
387,590 |
|
|
|
|
|
|
|||||
|
Three Months Ended |
|||||||
|
2020 |
|
2019 |
|||||
GAAP other (expense) income, net |
$ |
(61,130 |
) |
|
$ |
42,610 |
|
|
Decrease (increase) in fair value of strategic investments (1) |
44,870 |
|
|
(43,551 |
) |
|||
Non-GAAP other expense, net |
$ |
(16,260 |
) |
|
$ |
(941 |
) |
|
|
|
|
|
|||||
GAAP provision for income taxes |
$ |
54,781 |
|
|
$ |
51,534 |
|
|
Tax adjustments (5) |
129,608 |
|
|
29,392 |
|
|||
Non-GAAP provision for income taxes (6) |
$ |
184,389 |
$ |
80,926 |
Condensed Consolidated Balance Sheets (in thousands) (unaudited) |
||||||||
|
|
|
|
|||||
Assets |
|
|
|
|||||
Cash, cash equivalents and marketable securities |
$ |
4,190,396 |
|
|
$ |
3,808,294 |
|
|
Accounts receivable, net |
845,269 |
|
|
633,518 |
|
|||
Inventories |
187,087 |
|
|
167,502 |
|
|||
Property and equipment, net |
736,303 |
|
|
745,080 |
|
|||
|
1,402,158 |
|
|
1,402,158 |
|
|||
Deferred tax assets |
1,147,705 |
|
|
1,190,815 |
|
|||
Other assets |
384,283 |
|
|
371,098 |
|
|||
Total assets |
$ |
8,893,201 |
|
|
$ |
8,318,465 |
|
|
|
|
|
|
|||||
Liabilities and Shareholders' Equity |
|
|
|
|||||
Accounts payable and accrued expenses |
$ |
1,358,974 |
|
|
$ |
1,204,522 |
|
|
Finance lease liabilities |
572,916 |
|
|
577,371 |
|
|||
Contingent consideration |
178,100 |
|
|
176,500 |
|
|||
Other liabilities |
321,557 |
|
|
274,828 |
|
|||
Shareholders' equity |
6,461,654 |
|
|
6,085,244 |
|
|||
Total liabilities and shareholders' equity |
$ |
8,893,201 |
|
|
$ |
8,318,465 |
|
|
|
|
|
|
|||||
Common shares outstanding |
259,079 |
|
|
258,993 |
|
Supplemental Income Tax Information (in thousands, except percentages) (unaudited) |
||||||||
|
Three Months Ended |
|||||||
|
2020 |
|
2019 |
|||||
Components of provision for income taxes related to: |
|
|
|
|||||
|
|
|
|
|||||
Cash paid or accrued for income taxes |
$ |
9,370 |
|
|
$ |
4,778 |
|
|
Provision for income taxes offset by net operating losses |
45,411 |
|
|
46,756 |
|
|||
GAAP provision for income taxes (6) |
$ |
54,781 |
|
|
$ |
51,534 |
|
|
|
|
|
|
|||||
Cash paid or accrued for income taxes |
$ |
9,370 |
|
|
$ |
4,778 |
|
|
Tax adjustments (5) |
129,608 |
|
|
29,392 |
|
|||
Provision for income taxes offset by net operating losses |
45,411 |
|
|
46,756 |
|
|||
Non-GAAP provision for income taxes (6) |
$ |
184,389 |
|
|
$ |
80,926 |
|
|
|
|
|
|
|||||
|
|
|
|
|||||
Effective tax rate reconciliation: |
|
|
|
|||||
GAAP effective tax rate |
8 |
% |
|
16 |
% |
|||
Impact of GAAP to Non-GAAP adjustments |
13 |
% |
|
5 |
% |
|||
Non-GAAP effective tax rate |
21 |
% |
|
21 |
% |
Notes and Explanations
1: "Other income, net" includes gains and losses related to changes in the fair value of the company's strategic investments.
2: During the three months ended
3: "Collaborative revenues and expenses" in the three months ended
4: "Acquisition-related costs" in the three months ended
5: In the three months ended
6: The company records a provision for income taxes on its pre-tax income using an effective tax rate approximating statutory rates. The provision includes a significant non-cash charge due to the company's ability to offset its pre-tax income against previously benefited net operating losses. The company expects a portion of its tax provision to represent a non-cash expense until its net operating losses have been fully utilized. As of
About
Founded in 1989 in
Special Note Regarding Forward-Looking Statements
This press release contains forward-looking statements as defined in the Private Securities Litigation Reform Act of 1995, including, without limitation,
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