HighGravityData

Gilead Sciences — Nov 6, 2024 release

Fiscal 2024 third-quarter results · 8-K Item 2.02 · Exhibit 99.1 · 0000882095-24-000025
Open on SEC.gov ↗
Showing in the filing
Diluted EPS
“$ 0.05”
Period
No period stated
Measure
GAAP-tied
Source
Guidance table
All guidance in this release · 7
Product sales
“$ 27,800”
Product sales excluding Veklury
“$ 26,000”
Veklury for FY2024
“$1,800”
Diluted EPS
“$ 0.05”
Non-GAAP diluted EPS
“$ 4.25”
Quarterly dividend for Q4 FY2024
“$0.77 per share”
Quarterly dividend of common stock for Q4 FY2024
“$0.77 per share”
Exhibit 99.1 · the passage around this item
… earlier in the release
Guidance and Outlook For the full-year 2024, Gilead expects: (in millions, except per share amounts) November 6, 2024 Guidance Low End High End Comparison to August 8, 2024 Guidance Product sales $ 27,800  $ 28,100  Previously $27,100 to $27,500 Product sales, excluding Veklury $ 26,000  $ 26,300  Previously $25,800 to $26,200 Veklury $ 1,800  $ 1,800  Previously $1,300 Diluted EPS $ 0.05  $ 0.25  Previously $0.00 to $0.30 Non-GAAP diluted EPS $ 4.25  $ 4.45  Previously $3.60 to $3.90 Additional information and a reconciliation between GAAP and non-GAAP financial information for the 2024 guidance is provided in the accompanying tables. The financial guidance is subject to a number of risks and uncertainties. See the Forward-Looking Statements section below. Key Updates Since Our Last Quarterly Release Virology • Announced results of PURPOSE 2, the second Phase 3 study of twice-yearly lenacapavir for HIV prevention, with data presented at the HIV Research for Prevention Conference. In the lenacapavir group, 99.9% of participants did not acquire HIV infection, with 2 incident cases among 2,179 participants. Lenacapavir reduced HIV infections by 96% compared to background HIV incidence in cisgender men and gender-diverse people, and additionally demonstrated superiority to daily Truvada® (FTC 200mg and tenofovir disoproxil fumarate 300mg; 89% relative risk reduction). Lenacapavir was generally well-tolerated and no significant or new safety concerns were identified. Gilead expects to file for U.S. Food and Drug Administration (“FDA”) approval before the end of the yea
later in the release …
the item shown at left
other guidance in this release
Text is the filed exhibit, verbatim.