Clinical Study on the Safety and Efficacy of QN-030a in Acute Myeloid Leukemia

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 1
SUMMARY

This is an open-label, Phase I study of QN-030a (allogeneic NK cell therapy) in relapse/refractory Acute Myeloid Leukemia (AML). This clinical study is to evaluate the safety, tolerability and preliminary efficacy of QN-030a in patients with r/r AML, where a 3+3 enrollment schema will be utilized at dose escalation stage. Up to 18 patients will be enrolled.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Provision of signed and dated informed consent form (ICF)

• ≥18 years old

• Diagnosis of r/r AML

• Eastern Cooperative Oncology Group (ECOG) performance status ≤1

• Adequate organ function as defined in the protocol

• Donor specific antibody (DSA) to QN-030a: MFI \<= 2000

Locations
Other Locations
China
The first affiliated hospital of medical college of zhejiang university
RECRUITING
Hangzhou
Contact Information
Primary
He Huang, PhD
hehuangyu@126.com
86-13605714822
Backup
Yongxian Hu, PhD
huyongxian2000@aliyun.com
+8615957162012
Time Frame
Start Date: 2022-12-24
Estimated Completion Date: 2025-12-24
Participants
Target number of participants: 18
Treatments
Experimental: QN-030a
QN-030a in Adult subjects with r/r AML
Related Therapeutic Areas
Sponsors
Collaborators: Hangzhou Qihan Biotech Co.,Ltd.
Leads: Zhejiang University

This content was sourced from clinicaltrials.gov