The Citizens Life Sciences Conference 2026
Logotype for ACADIA Pharmaceuticals Inc

ACADIA Pharmaceuticals (ACAD) The Citizens Life Sciences Conference 2026 summary

Event summary combining transcript, slides, and related documents.

Logotype for ACADIA Pharmaceuticals Inc

The Citizens Life Sciences Conference 2026 summary

11 Mar, 2026

Commercial performance and financial position

  • Achieved over $1 billion in combined net sales from two commercial assets, with 2024 guidance at $1.25 billion midpoint.

  • Cash flow positive with over $800 million in cash and no debt, supporting both commercial and pipeline investments.

  • NUPLAZID saw 9% volume growth last year, driven by renewed direct-to-consumer campaigns and increased community awareness.

  • DAYBUE stabilized after initial plateau, with renewed growth following a 30% field force expansion and new formulation launch.

  • Persistency for DAYBUE is strong, with 55% of patients remaining on therapy at 12 months and over 45% at 18 months.

Pipeline and clinical development updates

  • Remlifanserin phase II trial for Alzheimer's disease psychosis expected to read out between August and October 2024.

  • Lessons from prior trials are being applied to optimize patient selection, outcome measures, and rater training for remlifanserin.

  • ACP-211, a deuterated ketamine metabolite, is in early clinical development for major depressive disorder, aiming for rapid onset and improved tolerability.

  • GABA alpha-3 program for essential tremor is completing phase I, with phase II proof-of-concept study planned for late 2024 or early 2025.

  • ACP-2591, a new Rett syndrome asset, is preparing for clinical testing and offers higher brain penetration than trofinetide.

Market expansion and product innovation

  • NUPLAZID growth is primarily volume-driven, with a small price benefit, and expansion efforts target both community and long-term care settings.

  • DAYBUE STIX, a new formulation, addresses administration challenges and is expected to reach an incremental 400 patients.

  • DAYBUE is available to 6,000 diagnosed Rett patients in the US, with about 1,000 currently on therapy and 2,000 having tried it.

  • International expansion for DAYBUE faces regulatory hurdles in Europe, with a re-examination underway after initial CHMP rejection.

  • Business development remains a priority to further broaden the portfolio.

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