Condition (MeSH)
Uniparental Disomy
ClinicalTrials.gov lists 1 trial for Uniparental Disomy or a narrower condition beneath it.
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Rows recorded per section
5 sections measured, none recorded · 1 not measured yet · 1 not computed
1 of the 1 trial is tagged with Uniparental Disomy itself; the rest are tagged with a narrower condition beneath it.
When did Uniparental Disomy trials start? (1)
Shown in this order: most recent first, 1990 onwards. 2026 is partial: trials registered with a 2026 start date so far, not a full year.
| Year | Trials started |
|---|---|
| 2013 | 1 |
No forecast is made for this condition: it averages 0.0 trial starts a year over the five years to September, under the 5 a year the method needs.
Recruitment duration, a model prediction: none of the 1 trial evaluated at the 2026-10-09 snapshot is predicted and still running. Source: ClinicalTrials.gov / AACT (CTTI), public domain.
What phase are Uniparental Disomy trials in? (1)
Shown in this order: phase order.
| Phase | Trials |
|---|---|
| Observational | 1 |
How many Uniparental Disomy trials are recruiting? (1)
Shown in this order: the order a trial moves through, from not yet recruiting to unknown.
| Status | Trials |
|---|---|
| Completed | 1 |
Status as registered on ClinicalTrials.gov. Each trial is counted once.
Which publications cover Uniparental Disomy? (16)
Shown in this order: major-topic papers first, then newest, then most linked to trials.
| Publication | Journal | Year | Major topic |
|---|---|---|---|
| Genetic Characterization and Prognostic Relevance of Acquired Uniparental Disomies in Cytogenetically Normal Acute Myeloid Leukemia. | Clinical cancer research : an official journal of the American Association for Cancer Research | 2019 | Yes |
| Spontaneous remission in a Diamond-Blackfan anaemia patient due to a revertant uniparental disomy ablating a de novo RPS19 mutation. | British journal of haematology | 2019 | Yes |
| Uniparental disomy unveils a novel recessive mutation in POMT2. | Neuromuscular disorders : NMD | 2018 | Yes |
| Constitutional Trisomy 8 Mosaicism with Persistent Macrocytosis. | Cytogenetic and genome research | 2016 | Yes |
| Eating behavior, prenatal and postnatal growth in Angelman syndrome. | Research in developmental disabilities | 2014 | Yes |
Showing 5 of 16 publications.
Not on this page
Not measured: delivery record.
Checked, with nothing recorded for this condition: lead sponsors, serious adverse events in this condition's trials, prevalence, rare-disease identity, and sub-conditions in mesh.
Not computed for conditions with fewer than 10 trials: drugs tested.