Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT07294300

A Phase I Trial of QLS2313 Injection in Relapsed/Refractory Hematological Malignancies

A Phase I Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Preliminary Efficacy of QLS2313 for Injection in Patients With Relapsed/Refractory Hematological Malignancies

Status
Not Yet Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
124 (estimated)
Sponsor
Qilu Pharmaceutical Co., Ltd. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This study is an open-label, dose-escalation and efficacy-expansion Phase I clinical trial to evaluate the safety, tolerability, PK profile, immunogenicity, and preliminary antitumor activity of QLS2313 as a monotherapy in patients with relapsed/refractory hematological malignancies.

Conditions

Interventions

TypeNameDescription
DRUGQLS2313CD79b/CD3/CD20;first in human; subcutaneous injection

Timeline

Start date
2026-01-01
Primary completion
2028-02-01
Completion
2028-02-01
First posted
2025-12-19
Last updated
2025-12-19

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT07294300. Inclusion in this directory is not an endorsement.