drugset / Trial / NCT02869243
A Dose Escalation Phase I Study Of Human- Recombinant Bone Morphogenetic Protein 4 Administrated Via CED In GBM Patients
NaSingle-groupOpen-labelTreatment
Summary
The purpose of the study is to evaluate the feasibility and safety of intra-tumor and interstitial therapy with hBMP4 in increasing doses in patients with progressive and/or multiple recurrent Glioblastoma multiforme (GBM).
Timeline
- Start
- 2017-07-18
- Primary completion
- 2020-10-16
- Completion
- 2021-06-30
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | human recombinant Bone Morphogenetic Protein 4 | Protein / enzyme biologic | 0.5 mg | Other |
| Subject | human recombinant Bone Morphogenetic Protein 4 | Protein / enzyme biologic | 18 mg | Other |