Gilead Sciences Guides Up
January 11, 2021
Gilead Sciences has revised
certain elements of its full year 2020 guidance.
Updated Full Year 2020 Guidance
(In
millions, except percentages and per share amounts)
|
Previously Updated
October 28, 2020 |
Updated
January 11, 2021 |
Product
Sales |
$23,000 - $23,500 |
$24,300 - $24,350 |
Product
Sales excluding Veklury |
|
$21,500 - $21,525 |
Veklury
|
|
$2,800 - $2,825 |
Non-GAAP
|
|
|
Product
Gross Margin |
86% - 87% |
~ 86.5% |
R&D
Expenses |
Mid-teens percentage growth |
~ 20% growth |
SG&A
Expenses |
Low double-digit percentage growth |
~ 10% growth |
Operating
Income |
$10,700 - $11,200 |
$11,650 - $11,750 |
Effective
Tax Rate |
~ 20% |
~ 19.0% - 19.5% |
Diluted
EPS |
$6.25 - $6.60 |
$6.98 - $7.08 |
GAAP
Diluted Earnings (Loss) Per Share |
$(0.25) - $0.10 |
$(0.08) - $0.02 |
The following provides
additional details on the company’s updated guidance:
-
Gilead
delivered solid performance, despite the global impacts of
COVID-19.
- Total product sales
guidance range is now $24.30 billion to $24.35 billion,
reflecting increased Veklury® (remdesivir) sales
as hospitalization and treatment rates were higher than
expected given the most recent COVID-19 surge.
- As a reminder, full year
2020 total product sales excluding Veklury reflects the
underlying strong Biktarvy® (bictegravir 50 mg/emtricitabine
200 mg/tenofovir alafenamide 25 mg) uptake, partially offset
by the Truvada® (emtricitabine 200 mg/tenofovir
disoproxil fumarate 300 mg) loss of exclusivity in the
United States and the impact of COVID-19 primarily on
Gilead’s pre-exposure prophylaxis (“PrEP”) franchise and
chronic hepatitis C virus (“HCV”) franchise.
- Guidance for Research and
development (“R&D”) expense changed to reflect the increase
in expense for obligations under the previously disclosed
new commercialization and development agreement for Jyseleca®
(filgotinib) with Galapagos NV. In addition, R&D expense for
the full year 2020 reflects growth due to higher clinical
trial and manufacturing ramp-up expenses related to Gilead’s
COVID-19 treatment remdesivir.
- Selling, general and
administrative (“SG&A”) expense reflects the low-end of
Gilead’s previous guidance. As a reminder, SG&A expense grew
for the full year 2020 due to a legal accrual related to a
previously disclosed legal settlement, expenses associated
with the acquisitions of Forty Seven, Inc. and Immunomedics,
Inc., and certain remdesivir donations.
- GAAP Diluted EPS guidance
is ($0.08) to $0.02 and Non-GAAP Diluted EPS guidance is
$6.98 to $7.08 for full year 2020.
The updated 2020
guidance range provided in this document is based on Gilead’s
preliminary fourth quarter 2020 results, which are subject to
change in connection with the completion of the company’s final
closing procedures, final adjustments and other developments
that may arise in the course of the preparation or audit of its
financial statements. Gilead’s management will host a conference
call to discuss the company’s fourth quarter and full year 2020
results in the coming weeks.
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