ACADIA Pharmaceuticals (ACAD) Q1 2026 earnings summary
Event summary combining transcript, slides, and related documents.
Q1 2026 earnings summary
13 May, 2026Executive summary
Q1 2026 revenue reached $268.1 million, up 11% year-over-year, driven by 20% growth in DAYBUE sales and 6% growth in NUPLAZID sales, with strong uptake of DAYBUE STIX and robust cash reserves of $851.5 million.
Net income for Q1 2026 was $3.6 million, down from $19 million in Q1 2025, primarily due to higher SG&A expenses.
DAYBUE STIX launched with strong early uptake, accounting for over 250 prescriptions in Q1, with ~30% from new or returning patients.
Pipeline progress includes anticipated phase II topline results for remlifanserin in Alzheimer's disease psychosis (ADP) in August–October 2026 and accelerated phase III trofinetide study in Japan.
Cash, cash equivalents, and investments totaled $851.5 million at quarter end, providing strong liquidity.
Financial highlights
Total Q1 2026 revenue: $268.1 million, up 11% year-over-year (adjusted).
DAYBUE net sales: $101.2 million, up 20% year-over-year; NUPLAZID net sales: $166.9 million, up 6% year-over-year (adjusted).
Gross to net adjustment: NUPLAZID at 22.1%, DAYBUE at 25.8%.
SG&A expenses increased to $171 million from $126.4 million, reflecting expanded commercial activities.
R&D expenses were $76.9 million, nearly flat year-over-year.
Outlook and guidance
Full-year 2026 total revenue guidance reaffirmed at $1.22–$1.28 billion.
NUPLAZID net sales expected at $760–$790 million; DAYBUE net sales at $460–$490 million.
R&D expense guidance: $385–$410 million; SG&A expense guidance: $660–$700 million.
Revenue expected to be back-end loaded, with greater sales in H2 2026 due to expanded field force and broader DAYBUE STIX adoption.
Anticipated topline results for remlifanserin (ADP) in August–October 2026 and trofinetide (Japan Phase 3) in September–November 2026.
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