Functional Implications of Rare Gene Mutations in aHUS Open the Door to Personalized Therapy
Functional Implications of Rare Gene Mutations in aHUS Open the Door to Personalized Therapy
Recruiting · NCT05805202 · Registry updated 2025-09-29Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Functional Implications of Rare Gene Mutations in aHUS Open the Door to Personalized Therapy | Cytopenia, Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications, Hemic and Lymphatic Diseases, Male Urogenital Diseases, Urogenital Diseases, anemia, atypical hemolytic-uremic syndrome, blood platelet disease, hematologic disorder, hemolytic anemia, hemolytic-uremic syndrome, kidney disorder, thrombocytopenia, thrombotic microangiopathy, uremia, urinary system disorder | Recruiting | Not applicable | 2025-09-29 | NCT05805202 |
1 results · Page 1 of 1
Organizations
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| Organizations | Linked trials |
|---|---|
| Mario Negri Institute for Pharmacological Research | 51 |
1 results · Page 1 of 1
Research sites
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| Research sites | City | Country | Linked trials |
|---|---|---|---|
| Centro di Ricerche Cliniche per le Malattie Rare "Aldo e Cele Daccò" | Ranica | Italy | 6 |