Calendario›CRMD›Taurolidine and Heparin
Taurolidine and Heparin
Expanded Access Program for Patients at Risk for Catheter-related Infections Who Are Not Eligible for DefenCath® Clinical Trials
Ensayo de CorMedix Inc. en Catheter-related Bloodstream Infection (del registro, en inglés).
- Fase
- no aplica
- Estado
- Ya no disponible
Qué significa cada fase y cada estado.
Estudio de acceso ampliado.
Cómo lo describe el promotor
En el documentoEn inglés, del registroThe EAP for DefenCath is designed to provide access to a broader population of adult and pediatric patients using catheters for various serious medical conditions. A key aspect of this EAP is its focus on individuals who, due to their unique clinical circumstances, are either ineligible for participation in ongoing clinical trials or do not meet the criteria outlined in the current approved FDA label for DefenCath.
Más ensayos de CRMD
| Ensayo | Fase | Estado | Lectura de resultados |
|---|---|---|---|
| Comparing The Safety And Efficacy Of DEFENCATH® In Reducing Central-Line Bloodstream Infections (CLABSIs) In Adults And Adolescent Participants Receiving Total Parenteral Nutrition Through A Central Venous Catheter (CVC) | Fase 3 | Reclutando pacientes | ene 2028 (prevista) |
| Open-Label Study to Assess Safety and Time to Catheter-related Bloodstream Infections (CRBSI) in Subjects From Birth to < 18 Years of Age | Fase 4 | Reclutando pacientes | jul 2028 (prevista) |
| Neutrolin | Fase 3 | Completado | oct 2018 (real) |
| deferiprone | Fase 3 | Retirado antes de empezar | mar 2013 (prevista, ya pasada: sin actualizar en el registro) |
| CRMD-001-Deferiprone | Fase 2 | Completado | jun 2011 (real) |
Todos los de CRMD, en su ficha.
Ficha completa en ClinicalTrials.gov (NCT06707480), actualizada en jun 2026.