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VES001

2 trials in this asset. Source: ClinicalTrials.gov, as of July 21, 2026.

Trials

2

Ongoing

0

Recruiting

0

Completed

2

Sites

3

Countries

2

Endpoints

40

Composite endpoints

0

Distinct sites and countries across this asset's trials. A site running several of its trials counts once, matching the map. All 40 linked ClinicalTrials.gov endpoints are classified into the categories below. Trial and endpoint linkage does not by itself establish treatment attribution for every endpoint.

Development

Where the program stands

Trials by phase

Phase 1
2

Trials by status

Completed
2

Evidence coverage

What this asset has been measured on

Endpoints grouped into outcome categories, ranked by how often they are measured across this asset's trials.

Safety / tolerability / PK
17
Fluid / digital biomarkers
12
Other (unclassified)
10
Behavior / neuropsychiatric
1

Most-measured metrics

Top 20 metrics across this asset's endpoints

Normalized metric codes are available for 0 of 40 classified ClinicalTrials.gov endpoints for this asset; the ranking below covers that coded subset.

No normalized metric codes are available for this asset.

Trials

Trials for this asset

Every trial for this asset, with the same search, filters, and sort as the Trials tab.

2 of 2

Alzheimer’s disease and related dementias trials
Asset / Disease areaKey I/E criterionEvidence
SORT-IN-2Study in Asymptomatic GRN-FTD Patients to Investigate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of VES001

VES001

Frontotemporal dementia

GRN mutation requiredPh 1Completed2Aug 2025-
SORT-IN-1A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of VES001 in Healthy Participants

VES001

Frontotemporal dementia

Age 18-55Ph 1Completed1Jul 2024-

Showing 1-2 of 2 trials