
Health Care · Biotechnology
$123.76
-1.35%
Vol: 5.2M
Friday, June 19, 2026
No material news in the last 48 hours.
Gilead Sciences received FDA approval of a supplemental new drug application for Yeztugo on June 15, 2026, adding to its growing HIV and liver disease portfolio. The company also paid its quarterly cash dividend of $0.82/share with an ex-date of June 15. Gilead is actively presenting at second-quarter 2026 investor conferences, signaling continued management engagement with the market. Russell Investments Group increased its holdings in GILD as of June 17, reflecting institutional buying interest. The stock traded in a range of $124.11-$128.20 on June 17, with a market cap of approximately $155.75 billion. No negative catalysts identified in the last 48 hours; the FDA approval is the most material near-term catalyst.
No material news in the last 48 hours.
No material news in the last 48 hours.
No material news in the last 48 hours.
Gilead announced positive topline results from its Phase 3 ISLEND-1 and ISLEND-2 studies of investigational oral once-weekly HIV treatment islatravir/lenacapavir, which met the primary efficacy endpoint with no new safety concerns. The stock rose 3.48% on June 11, 2026 on the pipeline momentum. Gilead also declared a quarterly cash dividend of $0.82 with an ex-date of June 15, 2026. Its HIV franchise, led by Biktarvy, remains the biggest growth engine, and management emphasized no major patent expiries until 2036. Of 31 analysts, the consensus rating is Buy with an average 12-month target of $157.83. The data strengthens Gilead's long-acting HIV pipeline against competition.
Gilead Sciences received FDA priority review for its once-daily bictegravir/lenacapavir HIV combination and continued returning capital through share repurchases. The company also filed a $6.51 billion common stock shelf registration to expand financial flexibility. Q1 2026 revenue reached $6.96 billion with net income of $2.02 billion, driven by 8% base business growth led by HIV, oncology, and liver disease. YEZTUGO and TRODELVY outperformed, prompting Gilead to raise 2026 revenue guidance by $400M. However, the company expects a 2026 adjusted loss of $0.65-$1.05/share (vs. prior EPS guidance of $8.45-$8.85) due to large acquisition-related charges. Truist raised target to $157. Average analyst target: $160.50 (~25.6% upside from $127.75). Gilead also extended its WHO collaboration on visceral leishmaniasis with 400,000+ vials of AmBisome donated through 2030.
Gilead reported Q1 2026 revenue of $6.96B with 8% YoY growth in the base business and 10% growth in HIV, supported by the launch of Yeztugo. Full-year 2026 revenue guidance was raised to $30.2B; however the company now expects an adjusted 2026 loss of $0.65 to $1.05 per share versus prior adjusted EPS guidance of $8.45-$8.85, reflecting one-time costs tied to the $7.8B Arcellx acquisition. Yeztugo full-year guidance was lifted from $800M to $1B, oncology now exceeds $3B annual run-rate, and Biktarvy holds over 52% U.S. HIV market share. Up to four launches and five Phase 3 updates are anticipated in 2026, including a potential anito-cel fourth-line approval that would validate the Arcellx deal. Jefferies has Buy/$180; Oppenheimer maintains Buy. Risk: integration and dilution from acquisitions plus pipeline binary outcomes.
Gilead executives are scheduled to present at the RBC Capital Markets Global Healthcare Conference on May 19 at 11 a.m. ET and the Bernstein Strategic Decisions Conference on May 28. Q1 2026 results posted revenue of $6.96B and adjusted EPS of $2.03 (vs. $1.91 est.), with raised product sales guidance, though full-year adjusted EPS guidance shifted to a loss of $0.65-$1.05 from prior $8.45-$8.85 due to acquisition-related charges. The company received FDA priority review for its once-daily bictegravir/lenacapavir HIV combination. Truist raised PT to $157 (Buy); Morgan Stanley lowered PT to $168 (Overweight). Risk: large IPR&D charges weigh on GAAP figures even as underlying HIV pipeline strengthens.
No material news in the last 48 hours.
Gilead launched its first investment-grade bond offering in 18 months, with notes in up to four tranches and maturities ranging two to eight years, to fund recent multibillion-dollar M&A including the $7.8 billion Arcellx acquisition plus Ouro Medicines and Tubulis. The FDA accepted Gilead's New Drug Application for its once-daily bictegravir/lenacapavir HIV regimen with priority review, a major commercial catalyst. Q1 2026 beat with $6.96B revenue and $2.03 adjusted EPS (vs $1.91 est), driven by 10% HIV growth led by Yeztugo launch and 8% base business growth. Full-year revenue guidance raised to $30.2B midpoint; however, full-year adjusted EPS guidance was lowered to -$0.85 midpoint due to acquisition-related costs (-110% change). Of 32 analysts, 18 Buy, 5 Outperform, 8 Hold, 0 Sell, with ~$158 mean target (~19% upside).
Gilead Sciences presented at the BofA Securities Healthcare Conference on Tuesday, May 12, 2026, with upcoming appearances at RBC Capital Markets Global Healthcare Conference (May 19) and Bernstein Annual Strategic Decisions Conference (May 28). The FDA accepted Gilead's New Drug Application for its once-daily bictegravir/lenacapavir HIV combination regimen with priority review, a key pipeline catalyst. Q1 2026 (reported May 7) revenue grew 4.4% YoY to $6.96B with non-GAAP EPS of $2.03 (beat by 6.3%), though revenue narrowly missed consensus of $7.05B; full-year revenue guidance maintained at ~$30.2B. The company completed a multi-year $4.57B share repurchase program and filed a $6.51B common stock shelf registration. Truist raised PT to $157 from $155. Risk: revised EPS forecast of $(1.05)-$(0.65) reflects substantial acquisition-related charges, creating an earnings optics overhang despite operating strength.
Gilead reported Q1 2026 revenue of $6.96B (+4.4% YoY) and adjusted EPS of $2.03 (6.3% above consensus), while completing a $4.57B share repurchase program and filing a $6.51B shelf registration. The FDA accepted Gilead's NDA for once-daily bictegravir/lenacapavir HIV regimen with priority review. However, full-year EPS guidance was sharply lowered due to $11.5B in IPR&D acquisition charges. Stock sits 17% below 52-week high of $157.29. Morgan Stanley lowered target to $168 from $175 on May 10. Analyst coverage: 18 Buy, 5 Outperform, 8 Hold.
Gilead reported Q1 2026 revenue of $6.96B (+4.4% YoY) and non-GAAP EPS of $2.03, beating the $1.95 consensus by $0.08. The FDA accepted Gilead's NDA for its once-daily bictegravir/lenacapavir HIV regimen with priority review, advancing the company's flagship HIV portfolio. Gilead also completed a multi-year $4.57B share repurchase program and filed a $6.51B shelf registration for up to 47.75M common shares, expanding financial flexibility. FY26 revenue guidance is maintained near $30.2B, though EPS guidance was sharply reduced due to large acquisition-related charges. Truist raised its price target to $157 from $155. Executives are presenting at BofA Healthcare (May 12), RBC Global Healthcare (May 19) and Bernstein Strategic Decisions (May 28).
| Company | Price | Day | 1M | Fwd P/E | Beta | Mkt Cap |
|---|---|---|---|---|---|---|
| ABBVABBVIE | $216.79 | -2.01% | +0.0% | 16.1x | 0.28 | $461.3B |
| AMGNAMGEN | $337.43 | -1.24% | +0.0% | 15.9x | 0.40 | $201.9B |
| GILDGILEAD | $123.76 | -1.35% | +0.0% | 13.6x | 0.34 | $163.0B |
| VRTXVERTEX | $451.94 | -1.54% | +0.0% | 24.6x | 0.29 | $134.0B |
| REGNREGENERON | $609.97 | +0.34% | +0.0% | 12.2x | 0.24 | $68.6B |
| BIIBBIOGEN | $196.51 | -1.09% | +0.0% | 13.0x | 0.16 | $31.9B |
Price below 200d MA — bearish structure.