drugset / Trial / NCT04033432
sEphB4-HSA in Treating Patients With Metastatic Castration-Resistant Prostate Cancer
Phase 2
Unknown
14 enrolled
Northwestern University
National Cancer Institute (NCI) · collabVasgene Therapeutics, Inc · collab
NaSingle-groupOpen-labelTreatment
Summary
The purpose of this phase II, single-arm, open-label, three center study is to evaluate the efficacy, safety, and tolerability of sEphB4-HSA in patients with mCRPC (metastatic castration-resistant prostate cancer). The study drug, sEphB4-HAS, is a form of protein that has not been approved for sale by the United States Food and Drug Administration (FDA). The study drug prevents tumor cells from multiplying and blocks several compounds that promote the growth of blood vessels that bring nutrients to the tumor.
Timeline
- Start
- 2019-09-20
- Primary completion
- 2021-02-05
- Completion
- 2022-06-30
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | sEphB4-HSA | Protein / enzyme biologic | 1000 mg | Intravenous |