Drugs / DNL593
last change Apr 2026 re-read 3 minutes ago

DNL593

Developed for
frontotemporal dementia
Investigated by
Denali Therapeutics Inc. · Takeda

Trials 1

202220232024202520262027
PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 1/2 NCT05262023 Feb 2022 → Dec 2026 expected frontotemporal dementia Denali Therapeutics Inc. Active not recruiting No outcome recorded

News releases announcing trial results or a regulatory action · 2

DateIssuerRelease
2025-01-13 Denali Therapeutics Inc. Results Denali Therapeutics Announces Key Anticipated 2025 Milestones and Priorities to Further Advance Its Therapeutics Portfolio for Neurodegeneration and Lysosomal Storage Diseases denalitherapeutics.com ↗
Data from the ongoing Phase 1/2 study of DNL593 have demonstrated dose-dependent increases in CSF progranulin levels, consistent with robust brain delivery of DNL593, in healthy volunteers.
2022-11-01 Denali Therapeutics Inc. Results Denali Therapeutics Announces Phase 1/2 Study Single Dose Healthy Volunteer Data with TAK-594/DNL593 (PTV:PGRN) and Progression to Enrolling Participants with FTD-GRN denalitherapeutics.com ↗
Single doses of DNL593 were generally well tolerated, based on blinded safety analysis.

Evidence & citations 1 cited value

Every value below carries the sentence it was read from. 1 source stands behind the page.

FieldValueCited text
Known as DNL593 ClinicalTrials.gov intervention name — accepted as the source's own label NCT05262023 ↗