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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
DE:DR6 Upcoming Earnings

ACADIA Pharmaceuticals's next earnings date is estimated for November 4, 2026, based on past reporting schedules.

Q2 2026 Earnings Call Audio

DE:DR6 Q2 2026 Earnings Call
0:00 / 0:00

Q2 2026 Earnings Slide Deck

Q2 2026 Earnings Call Summary

Q2 2026
Earnings Call Date:Aug 04, 2026|% Change Since:-16.75%|
Earnings Call Sentiment|Positive

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.

Company Guidance

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

DE:DR6 earnings history
Report DateFiscal QuarterForecast / EPSLast Year's EPSEPS YoY ChangePress Release
Nov 04, 20262026 (Q3)0.18-0.37――
Aug 04, 20262026 (Q2)0.060.160.1412.50% (+0.02)
May 06, 20262026 (Q1)0.050.020.1-81.82% (-0.08)
Feb 25, 20262025 (Q4)0.121.430.7786.05% (+0.66)
Nov 05, 20252025 (Q3)0.150.370.18110.00% (+0.20)
Aug 06, 20252025 (Q2)0.120.140.18-20.00% (-0.04)
May 07, 20252025 (Q1)0.080.100.0910.00% (+0.01)
Feb 26, 20252024 (Q4)0.190.770.25207.14% (+0.52)
Nov 06, 20242024 (Q3)0.120.18-0.36150.00% (+0.54)
Aug 06, 20242024 (Q2)0.160.180.011900.00% (+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.

Beat Missed
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