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GILD's Bictegravir and Lenacapavir Regimen for HIV Meets Primary Goal
ZACKS· 2025-12-16 14:56
Core Insights - Gilead Sciences, Inc. announced that its investigational single-tablet regimen of bictegravir and lenacapavir for HIV treatment met the primary endpoint in the ARTISTRY-2 study [1][6] Study Details - ARTISTRY-2 is a multicenter, double-blind, randomized phase III study comparing the safety and efficacy of the once-daily combination of bictegravir and lenacapavir (BIC/LEN) versus Biktarvy in virologically suppressed individuals with HIV [2] - The primary endpoint was the proportion of patients with HIV-1 RNA ≥50 copies/mL at week 48, and BIC/LEN was found to be statistically non-inferior to Biktarvy [3][10] Product Information - Bictegravir is a globally recommended integrase strand transfer inhibitor (INSTI) with a high barrier to resistance, while lenacapavir is approved for pre-exposure prophylaxis (PrEP) and treatment of multi-drug-resistant HIV [4][5] - The single-tablet regimen combining bictegravir and lenacapavir could reshape the HIV treatment landscape by providing more options for maintaining virologic suppression [6] Market Position - Gilead has a leading HIV franchise, with Biktarvy accounting for over 52% of the treatment market in the U.S. and Descovy holding more than 45% of the U.S. PrEP market [8][9] - The approval of lenacapavir as a twice-yearly injectable option for HIV prevention enhances Gilead's portfolio, especially as it faces competition from generics [11][12] Financial Performance - Yeztugo, the brand name for lenacapavir, generated $39 million in sales in the third quarter, achieving a 75% coverage goal ahead of schedule [13] - Gilead's shares have increased by 29.7% year to date, outperforming the industry growth of 18.9% [11] Competitive Landscape - Positive data from the ARTISTRY studies is expected to strengthen Gilead's HIV franchise amid increasing competition from companies like GSK, which is expanding its HIV business with long-acting injectable medicines [14]
Gilead(GILD) - 2025 FY - Earnings Call Transcript
2025-12-02 17:17
Financial Data and Key Metrics Changes - The company guided for approximately $150 million in sales for the first half of the year, with less than $100 million expected for the fourth quarter, indicating a strong start to the launch [2] - The operating margin improved to roughly 50% in the third quarter, reflecting a disciplined cost focus and operational efficiency [36][39] Business Line Data and Key Metrics Changes - The HIV prevention business collectively grew 42% year over year, with Descovy growing 32% year over year in HIV prevention [6] - Sunlenca's launch is expected to drive steady, consistent, durable growth similar to Biktarvy, which had $3.5 billion in sales in the third quarter [3] Market Data and Key Metrics Changes - The CDC estimates that at least 2.2 million people in the U.S. would benefit from HIV prevention, indicating a significant market opportunity [8] - Currently, about 500,000 people are on HIV prevention therapy, suggesting substantial room for growth in the market [12] Company Strategy and Development Direction - The company is focused on changing prescriber habits and building awareness for the new injectable options versus oral medications [2][5] - There is a strong emphasis on expanding the HIV prevention market, with plans for specific advertising campaigns to raise awareness [5][11] Management's Comments on Operating Environment and Future Outlook - Management expressed confidence in the long-term growth potential of the HIV prevention market, noting that the market is just beginning to develop [7][9] - The company highlighted the importance of building awareness and transitioning patients from existing therapies to new options [12][13] Other Important Information - The patent settlement for Biktarvy extends exclusivity until at least 2036, providing long-term stability for the company [15] - The company has a deep pipeline of next-generation HIV treatment alternatives, with multiple programs in clinical development [16][18] Q&A Session Summary Question: Can you discuss the strategy for educating patients and physicians on the benefits of the injectable option? - Management acknowledged that changing habits takes time and emphasized the importance of building a sales force and healthcare educators to raise awareness [5] Question: Where is the demand for Sunlenca coming from in the early days of the launch? - The company noted that there has been a surprising number of naive patients starting on Sunlenca, as well as patients switching from generic Truvada and other long-acting options [10][11] Question: What are the plans for Anito-cel and its market potential? - Management indicated that Anito-cel is expected to launch in the fourth-line plus market by the end of next year, with significant growth opportunities in multiple myeloma [24][25] Question: Can you provide an update on Trodelvy's regulatory submissions and growth potential? - The company expects updated label expansion filings for Trodelvy in the U.S. next year, which should drive significant growth [28] Question: How is the company approaching business development, particularly in China? - Management highlighted a shift towards more innovative assets in China and noted that a significant portion of their corporate development interest is now sourced from that region [33][34]