ACADIA Pharmaceuticals (DR6) Q2 2026 Earnings Report
DE:DR6 Q2 2026 EPS Results
- Actual EPS
- EUR 0.16
- Consensus EPS
- EUR 0.06
- Beat/Miss
- Beat by +EUR 0.10
- One Year Ago EPS
- EUR 0.14
DE:DR6 Q2 2026 Revenue Results
- Actual Revenue
- EUR 274.82M
- Expected Revenue
- EUR 264.64M
- Beat/Miss
- Beat by +EUR 10.18M
- YoY Revenue Growth
- +16.40%
Earnings Announcement Details
- Quarter
- Q2 2026
- Date
- 08/04/2026
- Time
- After Close
- Conference Call
- Tuesday, August 4, 2026
ACADIA Pharmaceuticals's next earnings date is estimated for November 4, 2026, based on past reporting schedules.
Q2 2026 Earnings Call Audio
Q2 2026 Earnings Slide Deck
Q2 2026 Earnings Call Summary
The call conveyed strong commercial momentum and clear near-term catalysts: robust Q2 results (total revenues +17%), pronounced DAYBUE STIX uptake (DAYBUE +30% YoY), healthy NUPLAZID growth (+10% YoY) with new prescriptions up 20%, a positive CHMP opinion for trofinetide in Europe, and significant pipeline progress (remlifanserin Phase II enrollment complete, Fast Track designation, top-line data expected Sep–Oct 2026). Offsetting factors include rising SG&A, sizable gross‑to‑net adjustments (~24%), a lowered R&D spend guidance due to a shifted BD milestone, reimbursement and pricing uncertainties in Europe, and dependency on upcoming pivotal readouts (creating execution/timing risk). Overall, the positives — strong sales, upgraded DAYBUE guidance, regulatory wins and a deepening pipeline with imminent binary catalysts — outweigh the operational and timing risks presented.
ACADIA raised its 2026 DAYBUE guidance to $480–$510M (from $460–$490) while keeping NUPLAZID at $760–$790M, implying total 2026 revenue of $1.24–$1.30B; Q2 results included total revenues of $308M (+17% adjusted YoY), DAYBUE net sales $125M (+30% YoY; ~27% of the increase from volume; ~40% of U.S. DAYBUE patients on STIX by quarter‑end and strong June STIX referral momentum), NUPLAZID net sales $183M (+10% adjusted YoY; 8% volume growth; new patient prescriptions +20% YoY and >12,000 priority HCPs reached since February), Q2 gross‑to‑net of 24.4% for DAYBUE and 23.9% for NUPLAZID (DAYBUE FY gross‑to‑net now guided to 23–25%), operating spend highlights of R&D $82M and SG&A $160M in Q2 with R&D guidance lowered to $355–$380M (from $385–$410M) due to a shifted BD milestone, cash of $956M, and pipeline timing/guidance that includes remlifanserin Phase II top‑line in Sept–Oct (Phase II enrollment 363; 80% powered to a 0.4 effect size; peak sales est. ~$4B, ~60% ADP/40% LBD), trofinetide Japan readout Sept–Nov and expected initial EU commercial sales/Q4 pending EC decision after a positive CHMP opinion, plus longer‑term ambitions of $700M DAYBUE and ~$1B NUPLAZID in 2028.
- Strong Q2 Financial PerformanceTotal revenues of $308 million in Q2 2026, representing +17% year-over-year on an adjusted basis; company now guiding full-year 2026 revenues of $1.24 billion to $1.30 billion.
- DAYBUE Sales Acceleration and U.S. STIX UptakeDAYBUE net sales were $125 million in Q2 (+30% YoY), with ~27% of that growth attributable to volume; approximately 40% of U.S. DAYBUE patients were receiving DAYBUE STIX by quarter end; DAYBUE 2026 guidance raised to $480M–$510M (from $460M–$490M) and management reiterated a $700M sales ambition for 2028.
- NUPLAZID Continued MomentumNUPLAZID net sales were $183 million in Q2 (+10% YoY on an adjusted basis), driven by ~8% volume growth; new patient prescriptions increased ~20% YoY (highest quarterly volume since Q1 2018); NUPLAZID full‑year guidance unchanged at $760M–$790M; expanded field force has reached over 12,000 priority HCPs since February.
- Pipeline Progress — remlifanserinPhase II enrollment for remlifanserin in Alzheimer's disease psychosis (RADIANT) is complete (Phase II portion enrolled 363 patients); the program received FDA Fast Track designation; top-line Phase II results are expected in September–October 2026; Phase III screening/enrollment has commenced; company cites peak sales potential of ~$4 billion across ADP and Lewy body dementia psychosis (management's rough split ~60% ADP / 40% LBD).
- Regulatory Milestones for Trofinetide (DAYBUE)Positive CHMP opinion received following re-examination for Rett syndrome in the EU; European Commission decision expected in Q3 2026 with a planned Germany launch in early Q4; trofinetide Phase III readout in Japan expected in Sep–Nov 2026 and a regulatory submission in Japan planned for 2027; named patient supply programs remain a contributor to international growth.
- Cash Position and Financial FlexibilityCash balance of $956 million at quarter end, providing runway and flexibility to fund commercial growth, advance the pipeline and pursue business development opportunities.
- Refined R&D PrioritizationR&D spend guidance lowered to $355M–$380M (from $385M–$410M), reflecting portfolio prioritization and shifting of a BD milestone to 2027 — indicates cost discipline while keeping key programs active.
DE:DR6 Earnings History
| Report Date | Fiscal Quarter | Forecast / EPS | Last Year's EPS | EPS YoY Change | Press Release |
|---|---|---|---|---|---|
| Nov 04, 2026 | 2026 (Q3) | 0.18- | 0.37 | ― | ― |
| Aug 04, 2026 | 2026 (Q2) | 0.060.16 | 0.14 | 12.50% (+0.02) | |
| May 06, 2026 | 2026 (Q1) | 0.050.02 | 0.1 | -81.82% (-0.08) | |
| Feb 25, 2026 | 2025 (Q4) | 0.121.43 | 0.77 | 86.05% (+0.66) | |
| Nov 05, 2025 | 2025 (Q3) | 0.150.37 | 0.18 | 110.00% (+0.20) | |
| Aug 06, 2025 | 2025 (Q2) | 0.120.14 | 0.18 | -20.00% (-0.04) | |
| May 07, 2025 | 2025 (Q1) | 0.080.10 | 0.09 | 10.00% (+0.01) | |
| Feb 26, 2025 | 2024 (Q4) | 0.190.77 | 0.25 | 207.14% (+0.52) | |
| Nov 06, 2024 | 2024 (Q3) | 0.120.18 | -0.36 | 150.00% (+0.54) | |
| Aug 06, 2024 | 2024 (Q2) | 0.160.18 | 0.01 | 1900.00% (+0.17) |
The table shows recent earnings report dates and whether the forecast was beat or missed. See the change in forecast and EPS from the previous year.
