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Study of VP301 in Patients With Multiple Myeloma, Lymphoma, or Solid Tumors

Multiple Myeloma Clinical Trial

Official title:
A Phase 1 Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of VP301 in Patients With Relapsed or Refractory Multiple Myeloma, Lymphoma, or Solid Tumors

Clinical Trial Summary

This study will test the safety, tolerability, and pharmacokinetics of VP301 in patients with relapsed or refractory multiple myeloma, lymphoma, or solid tumors.

Clinical Trial Description

This study will test the safety, tolerability, and pharmacokinetics of VP301 in patients with relapsed or refractory multiple myeloma, lymphoma, or solid tumors. This study will be conducted in two parts: Dose Escalation - This part will evaluate increasing doses of VP301 to identify the maximum tolerated dose (MTD) or recommended Phase 2 dose (RP2D). The first patient enrolled on the study will receive the lowest dose of VP301. Once this dose is shown to be safe, an additional patient will be enrolled at the next higher dose. Patients will continue to be enrolled into either single or multiple patient groups receiving increasing doses until the MTD or RP2D is reached. Dose Expansion - Patients with relapsed myeloma and lymphoma will be enrolled and treated with VP301 at the MTD or RP2D. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05698888
Study type Interventional
Source Virtuoso BINco, Inc.
Contact
Status Terminated
Phase Phase 1
Start date November 29, 2022
Completion date June 19, 2023
View Details
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