acquired hemophilia A
diseaseOn this page
Also known as AHA
Summary
acquired hemophilia A (MONDO:0035735) is a disease and 12 clinical trials. Top therapeutic interventions include cyclophosphamide anhydrous, susoctocog alfa, and emicizumab. A subtype of acquired hemophilia — broader associated-gene and molecular evidence is on the parent page (see Disease family below).
At a glance
- Prevalence: Unknown (Europe) [Orphanet-validated]
- Clinical trials: 12
Clinical features
Epidemiology
Prevalence records
8 prevalence record(s), Orphanet:
| Type | Class | Value | Geography | Validation |
|---|---|---|---|---|
| Annual incidence | 1-9 / 1 000 000 | 0.1505 | Europe | Validated |
| Annual incidence | 1-9 / 100 000 | 0.141 | United Kingdom | Validated |
| Annual incidence | <1 / 1 000 000 | 0.0829 | Spain | Validated |
| Annual incidence | 1-9 / 1 000 000 | 0.6 | Germany | Validated |
| Annual incidence | 1-9 / 1 000 000 | 0.12 | Australia | Validated |
| Annual incidence | <1 / 1 000 000 | 0.097 | Japan | Validated |
| Annual incidence | 1-9 / 1 000 000 | 0.45 | Switzerland | Validated |
| Point prevalence | 1-9 / 1 000 000 | 0.3063 | Spain | Validated |
Identifiers
Disease identifiers
| Field | Value |
|---|---|
| Canonical name | acquired hemophilia A |
| Mondo ID | MONDO:0035735 |
| MeSH | C536392 |
| Orphanet | 599480 |
| NCIT | C35345 |
| UMLS | C0272325 |
| MedGen | 124426 |
| GARD | 0006405 |
| Is cancer (heuristic) | no |
Also known as: AHA
Disease family
This is a subtype of acquired hemophilia. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.
Classification path: disease › human disease › disease by body system or component › hematologic disorder › hemorrhagic disease › acquired hemophilia › acquired hemophilia A
Related subtypes (2): acquired hemophilia B, acquired factor XI deficiency
Genetics & variants
GWAS landscape
No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.
Variant details and genetic-evidence tiers
No tiered GWAS variants or ClinVar records for this disease.
Genes & proteins
No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).
Function
No pathway enrichment — requires an associated-gene cohort.
Therapeutics
No druggable-target or therapeutic data for this disease’s cohort.
Clinical trials & evidence
Clinical trials
Clinical trials: 12.
Phase distribution (across all retrieved trials)
| Phase | Trials |
|---|---|
| Not specified | 7 |
| PHASE2/PHASE3 | 2 |
| PHASE2 | 2 |
| PHASE4 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT03384277 | PHASE4 | COMPLETED | Trial of Acquired Haemophilia With Steroid Combined With Cyclophosphamide Versus Steroid Combined With Rituximab |
| NCT01178294 | PHASE2/PHASE3 | COMPLETED | Study of Modified Recombinant Factor VIII (OBI-1) in Subjects With Acquired Hemophilia A |
| NCT04580407 | PHASE2/PHASE3 | COMPLETED | Study of TAK-672 in Participants With Acquired Hemophilia A |
| NCT05345197 | PHASE2 | ACTIVE_NOT_RECRUITING | Emicizumab in Patients With Acquired Hemophilia A |
| NCT03700229 | PHASE2 | UNKNOWN | Study to Evaluate Rituximab and Bortezomib in Patients With Newly Diagnosed Acquired Hemophilia A |
| NCT06461533 | Not specified | RECRUITING | A Survey of Susoctocog Alfa (Genetical Recombination) in Participants With Acquired Haemophilia A |
| NCT06550882 | Not specified | RECRUITING | A Study of OBIZUR in Adults With Acquired Hemophilia A (AHA) in South Korea |
| NCT01090349 | Not specified | COMPLETED | Clinical Evaluation Of Remote Monitoring With Direct Alerts To Reduce Time From Event To Clinical Decision |
| NCT01968655 | Not specified | NO_LONGER_AVAILABLE | Expanded Access to B-Domain Deleted Recombinant Porcine Factor VIII (OBI-1) in the Treatment of Acquired Hemophilia A Due to Factor VIII Inhibitory Auto-antibodies |
| NCT02004873 | Not specified | COMPLETED | Micra Transcatheter Pacing Study |
| NCT02610127 | Not specified | COMPLETED | Post-Marketing Non-Interventional Safety Evaluation of Obizur in the Treatment of Bleeding Episodes for Patients With Acquired Hemophilia A |
| NCT03199794 | Not specified | COMPLETED | Prospective and Retrospective, Non-interventional Study to Evaluate the Safety and Effectiveness of Obizur in Real-life Practice |
Drugs tested across these trials (top 30)
| Molecule | Max phase | Trials referencing |
|---|---|---|
| CYCLOPHOSPHAMIDE ANHYDROUS | 4 | 3 |
| SUSOCTOCOG ALFA | 4 | 3 |
| EMICIZUMAB | 4 | 1 |
| RITUXIMAB | 4 | 1 |
Related Atlas pages
- Drugs: Cyclophosphamide, Susoctocog Alfa, Emicizumab, Rituximab