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ILX651
Study of ILX651 in Patients With Hormone-Refractory Prostate Cancer Previously Treated With Docetaxel
Ensayo de Sanofi en Hormone-refractory Prostate Cancer (del registro, en inglés).
- Fase
- Fase 2
- Estado
- Completado
- Participantes
- 40
- Centros
- 12
previstos
Qué significa cada fase y cada estado.
Estudio de intervención, no aleatorizado, abierto.
Cómo lo describe el promotor
En el documentoEn inglés, del registroThis is a Phase II, non-randomized, open label study of ILX651 in patients with hormone-refractory prostate cancer previously treated with docetaxel. Approximately 40 patients will be enrolled in this study that is expected to last 24 months. All patients will be treated with ILX651 administered IV daily for 5 consecutive days every 21 days. The primary objective of this study is to determine the PSA response rate. The secondary objectives are to determine response of measurable disease, duration of response, time to PSA progression, time to treatment failure, survival, safety and tolerability, and pharmacokinetic profile of ILX651.
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Ficha completa en ClinicalTrials.gov (NCT00082134), actualizada en mar 2015.