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Organization (Industry)

Denali Therapeutics Inc.

ClinicalTrials.gov lists Denali Therapeutics Inc. as lead sponsor of 19 trials. It has 20 active development programs and 1 approved asset.

US Industry Manufacturer CIK 0001714899
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6 0 2017 2026

Trials started per year with this organization as sponsor or collaborator, 1990 onward. The series also counts trials where the organization is a collaborator; the lead-sponsor trial count does not.

2026 is partial: 3 registered with a 2026 start date. The dashed outline is the pace from the 3 registered with a start date through September, planned starts included, not adjusted; not a forecast. No forecast is made for this organization: it averages 2.8 trial starts a year over the five years to September, under the 5 a year the method needs.

This page covers Denali Therapeutics Inc.: 19 lead-sponsored trials and 3 legal-entity registrations.

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Disease areas (12)

Shown in this order: most trials first.

Disease areas
Disease area Trials
Death 4
Dementia 4
Infant Death 4
Intellectual Disability 4
Mucopolysaccharidosis II 4

Trials by start year as sponsor or collaborator (9)

Shown in this order: most recent first. 2026 is partial: trials registered with a 2026 start date so far, not a full year.

Show the table of trials by start year as sponsor or collaborator
Trials by start year as sponsor or collaborator
Year Trials started
2026 (partial year) 3
2024 2
2023 3
2022 6
2021 3
2020 3
2019 2
2018 2
2017 2

Prediction, not a registry value: median of 36 months from start to primary completion across 8 trials still running at the 2026-10-09 snapshot; registered median of 13 months across 10 trials with a primary completion typed Actual. Source: ClinicalTrials.gov / AACT (CTTI), public domain.

Active development programs (20)

Shown in this order: max phase, then active trials.

Active development programs
Drug Disease area Max phase Trials
tividenofusp alfa Sudden Infant Death Phase 2/3 3
tividenofusp alfa Mucopolysaccharidosis II Phase 2/3 3
tividenofusp alfa Death Phase 2/3 3
tividenofusp alfa Intellectual Disability Phase 2/3 3
tividenofusp alfa Infant Death Phase 2/3 3

Approved assets (1)

Approved assets
Drug Trials
Idursulfase 1

Sponsor delivery record (1)

Enrollment hit target: the share of this sponsor's lead-sponsored trials whose actual enrollment reached the planned enrollment. On time: the share whose actual primary completion date was no later than the planned date. Each share counts only trials where we observed an estimated figure before the actual one, and n is that number of trials. Below 5 trials the count is shown as a fraction, not a percentage.

Sponsor delivery record
Enrollment Timeline
54% hit target (n=13) 22% on time (n=9)

Journals published in (5)

Shown in this order: most published in first.

Journals published in
Journal Publications
Clinical and translational science 1
Molecular neurodegeneration 1
Neural regeneration research 1
Nutritional neuroscience 1
The New England journal of medicine 1

US granted patents (1)

Patents are not classified by disease area in the source, so this is the organization's overall portfolio, not a split by disease.

US granted patents
US patents granted Granted in the last 5 years Most recent grant
52 34 2025-12-16

SEC-reported annual financials (11)

Shown in this order: newest fiscal year first; SEC EDGAR XBRL companyfacts, USD as reported.

SEC-reported annual financials
Fiscal year Revenue (USD) Net income (USD) R&D (USD)
2025 0 -512,540,000 418,778,000
2024 0 -422,773,000 396,440,000
2023 330,531,000 -145,224,000 423,876,000
2022 105,065,000 -325,991,000 358,732,000
2021 48,657,000 -290,581,000 265,353,000
2020 335,561,000 71,136,000 212,615,000
2019 26,320,000 -197,614,000 193,382,000
2018 129,100,000 -36,240,000 143,183,000
2017 0 -88,185,000 74,460,000
2016 0 -86,652,000 75,702,000

Financing and grant events (29)

Shown in this order: most recent first.

Financing and grant events
Date Round type Amount (USD) Source
2026-07-27 Other financing 195 Sec extracted
2026-06-12 Royalty / licensing not disclosed Sec extracted
2026-03-27 Royalty / licensing 200,000,000 Sec extracted
2025-12-10 Follow-on offering not disclosed Edgar offerings
2025-12-09 Other financing not disclosed Edgar offerings

Climate targets, as filed (1)

Climate targets, as filed
Reporting year Net-zero target
2025 not disclosed

Workforce and board diversity, as filed (1)

Workforce and board diversity, as filed
Reporting year Workforce % women Board % women
2025 not disclosed not disclosed

Organization relationships (2)

Shown in this order: most evidence first.

Organization relationships
Related organization Relationship Evidence
Sanguine Biosciences (United States) Co sponsors trial with 1
Merit E. Cudkowicz, MD Co sponsors trial with 1

Latest dated events (113)

Shown in this order: newest first.

Latest dated events
Date Event Source
2026-08-07 Trial started Clinical trials (ClinicalTrials.gov) (ClinicalTrials.gov, U.S. National Library of Medicine; AACT database, Clinical Trials Transformation Initiative (CTTI))
2026-07-27 Financing Funding rounds and grants (NIH RePORTER + SEC EDGAR)
2026-06-12 Royalty / licensing Funding rounds and grants (NIH RePORTER + SEC EDGAR)
2026-05-12 Trial started Clinical trials (ClinicalTrials.gov) (ClinicalTrials.gov, U.S. National Library of Medicine; AACT database, Clinical Trials Transformation Initiative (CTTI))
2026-04-05 PDUFA decision date Regulatory decision dates extracted from SEC filings

Biomarker capability evidence (24)

Shown in this order: tier desc, then gene symbol.

Biomarker capability evidence
Gene Role Evidence
ACHE Trial sponsor Named in trial inclusion criteria
APP Trial sponsor Named in trial inclusion criteria
GRN Trial sponsor Named in trial inclusion criteria
IDS Trial sponsor Named in trial inclusion criteria
IDS Trial sponsor Named in trial inclusion criteria

Not on this page

Checked, with nothing recorded for this organization: companies grouped under this page, related companies not grouped here, fda warning letters, fda untitled letters, fda inspection record, fda recalls, fda import refusals, manufacturing and distribution sites, clia clinical laboratory certificates, and biomarkers this organization publishes on.