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Condition (MeSH)

Spherocytosis, Hereditary

ClinicalTrials.gov lists 7 trials for Spherocytosis, Hereditary or a narrower condition beneath it.

MeSH D013103 Hemic and Lymphatic Diseases C15 C16 Listed by Orphanet as a rare disease
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Not applicable Not applicable 2 Observational Observational 5 Not applicable Not applicable 2 Observational Observational 5

Trials per phase

7 of the 7 trials are tagged with Spherocytosis, Hereditary itself; the rest are tagged with a narrower condition beneath it.

Get the Spherocytosis, Hereditary report as a PDF

The PDF carries up to 50 rows of each section, where the page shows the first few, with the sources listed. Enter a work email and confirm it from the message we send, and the report follows by email.

When did Spherocytosis, Hereditary trials start? (5)

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.

Trials over time, by phase

  • Not applicable
  • Observational

Top of scale: 3

2009: 1 trials (Not applicable 1) 2010: 1 trials (Observational 1) 2016: 1 trials (Observational 1) 2020: 3 trials (Observational 2, Not applicable 1)

Trials registered with a start date in each year, 1990 onward, stacked by phase (complete years only; the current partial year is in the table's notes). The table below lists the same counts, most recent years first.

Trials started per year
Year Trials started
2026 (partial year) 1
2020 3
2016 1
2010 1
2009 1

No forecast is made for this condition: it averages 0.2 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 7 trials evaluated at the 2026-10-09 snapshot is predicted and still running. Source: ClinicalTrials.gov / AACT (CTTI), public domain.

What phase are Spherocytosis, Hereditary trials in? (2)

Shown in this order: phase order.

Show the trials by phase as a table
Trials by phase
Phase Trials
Not applicable 2
Observational 5

How many Spherocytosis, Hereditary trials are recruiting? (5)

Shown in this order: the order a trial moves through, from not yet recruiting to unknown.

Trials by recruitment status
Status Trials
Not yet recruiting 1
Recruiting 2
Completed 2
Terminated 1
Withdrawn 1

Status as registered on ClinicalTrials.gov. Each trial is counted once.

Which publications cover Spherocytosis, Hereditary? (10)

Shown in this order: major-topic papers first, then newest, then most linked to trials.

Prevalence (9)

Shown in this order: jurisdiction, then disease name. Orphanet observation for the mapped ORPHA concept; the mapping relation column says whether that concept is exactly this condition or broader or narrower.

Prevalence
Orphanet disease Type Class Geography Jurisdiction Mapping relation
Hereditary spherocytosis Prevalence at birth 1-5 / 10 000 United States US Exact
Hereditary spherocytosis Prevalence at birth 1-5 / 10 000 United States US Exact
Hereditary spherocytosis Prevalence at birth 1-5 / 10 000 United States US Unspecified
Hereditary spherocytosis Point prevalence 1-5 / 10 000 Germany Not stated Unspecified
Hereditary spherocytosis Point prevalence 1-5 / 10 000 Europe Not stated Unspecified

Rare-disease identity (2)

Shown in this order: exact, broader, narrower, other.

Rare-disease identity
Orphanet disease ORPHA code Relation Source
Hereditary spherocytosis 822 Exact Orphadata Science knowledge files, Product 1
Hereditary spherocytosis 822 Exact Orphanet Rare Disease Ontology (ORDO)

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, and sub-conditions in mesh.

Not computed for conditions with fewer than 10 trials: drugs tested.

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