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Clinical Trial Summary

This is a phase Ia/Ib, first-in-Human, open-Label, multicenter, dose escalation and dose expansion study designed to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, immunogenicity, and preliminary efficacy of SG2501 in subjects with relapsed or refractory hematological malignancies and lymphoma.


Clinical Trial Description

Phase Ia will consist of two parts:an accelerated titration using single patient cohorts to evaluate SG2501 at lower dose levels(Part A), followed by dose-escalation using multipatient cohorts to establish a maximum tolerated dose(MTD)(Part B). Phase Ib will consist of dose expansion cohorts with SG2501 monotherapy in subjects with relapsed or refractory multiple myeloma(MM) or diffuse large B-cell lymphoma(DLBCL). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05293912
Study type Interventional
Source Hangzhou Sumgen Biotech Co., Ltd.
Contact Nashat Gabrail
Phone 330-492-3345
Email ngabrailmd@gabrailcancercenter.com
Status Recruiting
Phase Phase 1
Start date August 3, 2022
Completion date April 30, 2025

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