drugset / Trial / NCT00226668
XERECEPT® (hCRF) for Primary Glioma Patients Requiring Dexamethasone to Treat Peritumoral Brain Edema
Phase 3
Withdrawn
120 enrolled
Celtic Pharma Development Services
Neurobiological Technologies · collab
RandomizedParallel-groupTriple-blindTreatment
Summary
The purpose of this study is to examine the safety and efficacy of XERECEPT (human Corticotropin-Releasing Factor, or hCRF) compared to dexamethasone in patients with primary malignant glioma who require increased dexamethasone doses to control symptom of peritumoral brain edema.
Timeline
- Start
- 2006-01
- Primary completion
- —
- Completion
- 2008-01
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Xerecept | Unknown | 2 mg | — |