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Andrew Sy

Vice President and Equity Research Analyst at Jefferies

Andrew Sy is a Vice President and Equity Research Analyst at Jefferies, specializing in the technology sector with a focus on cloud infrastructure, enterprise software, and cybersecurity. He covers key companies including Snowflake (SNOW), CrowdStrike (CRWD), Zscaler (ZS), and MongoDB (MDB), boasting a strong performance track record with a 68% success rate on TipRanks, an average return of 22.3%, and ranking in the top 10% of analysts covering technology stocks. Sy joined Jefferies in 2021 after starting his career at JMP Securities as a research associate from 2018 to 2021, and he holds Series 7, 63, and 86/87 FINRA licenses. His insightful calls have earned him recognition on institutional investor ranking platforms for accurate forecasting in high-growth tech names.

Andrew Sy's questions to Vanda Pharmaceuticals (VNDA) leadership

Question · Q4 2025

Andrew Sy from Jefferies questioned the 2026 Fanapt guidance of $150-$170 million, asking if the implied 30% net price growth at the midpoint was accurate and why. He also inquired about the extent of cannibalization from Bysanti's Q3 launch factored into this guidance. Additionally, he asked about Nereus's anticipated list price, net price, and expected sales growth in its first four quarters post-launch. Finally, he sought details on the tradipitant GLP-1 phase 3 study design, expected efficacy, and the precedent for using a high upfront Wegovy dose.

Answer

Kevin Moran, CFO of Vanda Pharmaceuticals Inc., clarified that the Fanapt revenue growth for 2026 is almost entirely volume-driven, not price-driven, due to capped price increases. He stated that the 2026 guidance includes $0 revenue contribution from Bysanti. For Nereus, he mentioned NK-1 class doses range from $200-$600, and Vanda expects a premium price over existing motion sickness treatments, but did not provide specific guidance. Dr. Mihael Polymeropoulos, CEO, confirmed the tradipitant GLP-1 phase 3 design would be similar to phase 2, using a 1mg Wegovy challenge in naive patients, and explained that a higher challenge success implies efficacy at lower doses, despite Wegovy's typical slow titration.

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