
GILD · NASDAQ-GS
Expected to report Oct 29, 2026 — estimated from last year’s reporting date.
Consensus is $2.14 EPS for Sep 2026 across 6 estimates, ranging $1.84 to $2.30.
No consensus figures were provided, so the quarter cannot be assessed against an external earnings expectation. Revenue was solid, reaching $7.803 billion, up 10% year over year versus 7% growth in the first six months. HIV carried results, rising 12% to $5.693 billion on stronger Biktarvy, Descovy and Yeztugo demand and pricing. Liver Disease grew 10% to $877 million, while Trodelvy increased 26% to $457 million. These gains were partly offset by an 81% Veklury decline to $23 million and a 14% Cell Therapy decline to $417 million amid competitive pressure. Product gross margin held at 79.3%, with the reported quarterly comparison described as relatively flat. Profitability nevertheless collapsed to a $10.496 billion net loss from $1.960 billion of net income, driven by $11.183 billion of acquired IPR&D, a $1.750 billion impairment, and higher operating expenses. R&D rose 18% and SG&A 41%.
No financial guidance was given in the supplied material: management provided no revenue, earnings, margin, or capex ranges for the next quarter or full year, and no revisions to a prior financial guide were described. The forward-looking items were primarily regulatory milestones rather than operating targets. The FDA has a PDUFA target action date of August 27, 2026 for bictegravir and lenacapavir, December 23, 2026 for anito-cel, and February 2, 2027 for a potential once-weekly Yeztugo formulation. These dates remain subject to regulatory review and do not constitute financial guidance.