Medical Information Only. Consult your healthcare provider before considering clinical trial enrollment.
Autosomal Dominant Alzheimer Disease Due to Mutation of Presenilin 1 (Disorder): early-phase trial registry
1 of 1 indexed Autosomal Dominant Alzheimer Disease Due to Mutation of Presenilin 1 (Disorder) trials are currently recruiting, with more weight in Phase 1-2.
Corpus placement: #11,370 of 28,707 conditions by registered trial count.
1 US clinical trials · 1 currently recruiting · #11,370 of 28,707 conditions by registered trial count
Autosomal Dominant Alzheimer Disease Due to Mutation of Presenilin 1 (Disorder): 1 US clinical trial tracked, 1 recruiting.
Autosomal Dominant Alzheimer Disease Due to Mutation of Presenilin 1 (Disorder) is the subject of 1 registered US clinical trials on ClinicalTrials.gov, 1 of them currently open to new participants. 0 are in Phase 3-4 (later-stage) and 1 in Phase 1-2 (earlier-stage). The most active sponsor is University College, London, running 1 of these trials.
Enrollment posture brief
Registry condition autosomal-dominant-alzheimer-disease-due-to-mutation-of-presenilin-1-disorder
OPEN 1 | RECR 100% | LATE 0 | EARLY 1 | RANK #11370 | SPON 1
Volume-matched condition peers
Nearest open-share peer: Aortic Arch Aneurysm (100% recruiting · 5 trials)
Autosomal Dominant Alzheimer Disease Due to Mutation of Presenilin 1 (Disorder) lists 1 open slots (100% of 1 indexed trials). Peers are matched on registered volume, not therapeutic-area browse lists. How peer matching works →
Key findings
What ClinicalTrials.gov does not surface for Autosomal Dominant Alzheimer Disease Due to Mutation of Presenilin 1 (Disorder) on its own pages , computed from the registry mirror as of 2026-08-08. Each line carries its own denominator so it can be quoted as it stands.
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Autosomal Dominant Alzheimer Disease Due to Mutation of Presenilin 1 (Disorder) is recruiting above its size-band peers.
1 of 1 indexed trials (100%) are open to enrollment, against a 46.5% average across 27,806 conditions with fewer than 20 trials. The peer set uses the same ClinicalTrials.gov-derived counts as this page.
Open and recent trials
1 total, page 1 of 1
Phase Distribution
| Phase | Trial count |
|---|---|
| Phase 1 | 1 |
Top Sponsors
Named interventions
Most-linked intervention names on Autosomal Dominant Alzheimer Disease Due to Mutation of Presenilin 1 (Disorder) records (sponsor-reported on ClinicalTrials.gov). Counts are trial links, not unique products.
US sites by state
Facility locations filed on Autosomal Dominant Alzheimer Disease Due to Mutation of Presenilin 1 (Disorder) trials. A trial with sites in several states counts in each.
Source: ClinicalTrials.gov, National Library of Medicine. Data is informational only.
Related
What to do with this Autosomal Dominant Alzheimer Disease Due to Mutation of Presenilin 1 (Disorder) page
1 registered trials, 1 currently recruiting, is a starting point for a conversation, not a diagnosis or a recommendation.
- 1 Autosomal Dominant Alzheimer Disease Due to Mutation of Presenilin 1 (Disorder) trials are currently recruiting, check eligibility criteria before contacting a site. Browse recruiting trials
- University College, London sponsors the most Autosomal Dominant Alzheimer Disease Due to Mutation of Presenilin 1 (Disorder) trials on record, review their full trial history before evaluating a specific study. See University College, London's trials
- Bring the specific trial ID (NCT number) to your own doctor before enrolling, this page is a directory, not medical guidance. Read the trial-finding guide
Trial and recruiting counts reflect ClinicalTrials.gov registry status as of the data vintage above; individual trial eligibility and enrollment status can change.
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This Autosomal Dominant Alzheimer Disease Due to Mutation of Presenilin 1 (Disorder) condition card totals 1 registered trials; most-linked intervention NIO752; top US site state Missouri. See our editorial standards & corrections policy, the methodology behind these numbers, the data changelog, or report a data error.