drugset / Trial / NCT02869243

A Dose Escalation Phase I Study Of Human- Recombinant Bone Morphogenetic Protein 4 Administrated Via CED In GBM Patients

NCT02869243 ↗

Phase 1 Completed 15 enrolled Stemgen ORION Clinical Services · collab
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

EvaluationDrugModalityDoseRoute
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

Indications