Acadia Pharmaceuticals reported its Q1 2023 financial results, featuring the FDA approval and launch of DAYBUE for Rett syndrome and NUPLAZID net sales of $118.5 million, a 3% increase compared to Q1 2022. The company is also advancing its pipeline, including the completion of Phase 1 development for ACP-204 and nearing enrollment completion for the Phase 3 program for pimavanserin.
NUPLAZID net sales reached $118.5 million, a 3% increase compared to the same period last year.
DAYBUE received FDA approval for the treatment of Rett syndrome and was launched on April 17, 2023.
Phase 1 development program for ACP-204 has been completed.
Enrollment completion is nearing for the Phase 3 program for pimavanserin as a potential treatment for the negative symptoms of schizophrenia with top-line results expected in early 2024.
Acadia is reiterating all of its 2023 guidance provided on February 27, 2023.