Clinical trial

A Phase Ia/Ib Study Evaluating the Safety, Tolerability and Preliminary Efficacy of IBI322 in Subjects With Myeloid Tumor

Name
CIBI322A106
Description
This is a phase I study evaluating the safety, tolerability and preliminary efficacy of IBI322 in Myeloid tumor patients.
Trial arms
Trial start
2021-12-28
Estimated PCD
2023-06-19
Trial end
2023-08-29
Status
Terminated
Phase
Early phase I
Treatment
IBI322
Recombinant anti-human CD47/PD-L1 bispecific antibody
Arms:
IBI322
Size
1
Primary endpoint
Number of treatment related AEs
Up to 90 days post last dose
Eligibility criteria
Inclusion Criteria: 1. Patients who met the diagnostic criteria of recurrent / refractory AML (WHO 2016)(primordial cells in bone marrow ≥ 5%) (excluding APL and bcr-abl positive AML ) and underwent treatment. 2. Patients who meet the diagnostic criteria of recurrent / refractory MDS (WHO 2016)and underwent treatment. 3. Patients with recurrent / refractory Essential thrombocythemia (WHO2016) after treatment (for Phase Ia) 4. Male or female subject above 18 years old 5. Eastern Cooperative Oncology Group Performance Status (ECOG PS) performance status 0 \~ 2. 6. Must have adequate organ function Exclusion Criteria: 1. Previous history with myeloproliferative Neoplasms(MPN) or MDS/MPN 2. Transformation or treatment related AML/MDS. 3. PV/MF/AML/MDS evolved from Essential thrombocythemia 4. Relapse after allogeneic hematopoietic stem cell transplantation, or autologous hematopoietic stem cell transplantation within 1 year 5. Central nervous system leukemia infiltration 6. Previous history of chronic hemolytic anemia or screening Coombe test positive 7. Previous exposure to any anti-CD47 monoclonal antibody, SIRPα antibody, or CD47/SIRPα recombinant protein. 8. Previous exposure to chimeric antigen receptor T cell immunotherapy (CAR-T) 9. Patients who received immunotherapy, targeted therapy, biological therapy or any clinical research treatment within 14 days before receiving the first dose 10. Uncontrolled concurrent diseases 11. Subjects who are allergic to the ingredients of the study drug 12. Subjects who have used immunosuppressive drugs within 7 days before the first dose of study treatment
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE1'], 'designInfo': {'allocation': 'NA', 'interventionModel': 'SINGLE_GROUP', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'NONE'}}, 'enrollmentInfo': {'count': 1, 'type': 'ACTUAL'}}
Updated at
2023-09-08

1 organization

1 product

1 indication

Product
IBI322
Indication
Myeloid Tumor