A Study of sEphB4-HSA in Kaposi Sarcoma

Status Recruiting

Clinical Trial Summary

sEphB-HSA may prevent tumor cells from multiplying and blocks several compounds that promote the growth of blood vessels that bring nutrients to the tumor. The purpose of this study is to learn if sEphB4-HSA will decrease the number or size of Kaposi sarcoma lesions in people.

Clinical Trial Description

sEphB4-HSA will be given through an intravenous infusion (into a vein). Each cycle of sEphB4-HSA will be 28 days (4 weeks). Each cycle of the study drug includes administration of 2 doses of sEphB4-HSA given on Days 1 and 15 of each cycle. Participants may continue on study protocol as long as their KS is continuing to respond or is clinically stable on study medication. Patients may come off treatment for the following reasons: - Disease progression. - Need for more than 2 dose reductions for toxicity. - Dose delay more than 28 days. - Patient withdraws consent. - Study termination by the Sponsor. - Participants who are noncompliant with respect to taking drugs, keeping appointments, or having tests required for the evaluation of drug safety and efficacy. - Participant's condition renders them unacceptable for further treatment in the judgment of the investigator. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03993106
Study type	Interventional
Source	Vasgene Therapeutics, Inc
Contact	Sarah E. Cole, M.S.
Phone	626-840-7756
Email	scoleemail@gmail.com
Status	Recruiting
Phase	Phase 2
Start date	September 17, 2020
Completion date	June 2025

View Details

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