Overview
QL1706 is an investigational bifunctional antibody that combines the activity of both PD-1 and CTLA-4 antibodies.
Indication
No indication information available.
Associated Conditions
No associated conditions information available.
Research Report
QL1706 (Iparomlimab/Tuvonralimab): A Comprehensive Analysis of a Novel Bifunctional PD-1/CTLA-4 MabPair Immunotherapy
Executive Summary
QL1706 is a first-in-class, investigational bifunctional antibody product developed by Qilu Pharmaceutical Co., Ltd., representing a significant innovation in the field of cancer immunotherapy. Identified by the DrugBank ID DB17562 and the development code PSB205, QL1706 is not a single bispecific antibody but rather a co-formulated mixture of two distinct monoclonal antibodies: Tuvonralimab, an anti-Programmed Death-1 (PD-1) IgG4 antibody, and Iparomlimab, an anti-Cytotoxic T-Lymphocyte-Associated Protein 4 (CTLA-4) IgG1 antibody. This unique composition is achieved through the proprietary MabPair™ technology platform, which enables the production of both antibodies from a single cell line at a fixed ratio, ensuring consistent delivery and synergistic action.
The core therapeutic rationale of QL1706 is to harness the proven synergistic anti-tumor efficacy of dual PD-1 and CTLA-4 blockade while mitigating the significant immune-related toxicities that have limited the use of conventional combination therapies. This is achieved through sophisticated bioengineering of the Iparomlimab (anti-CTLA-4) component to possess a shorter elimination half-life compared to the Tuvonralimab (anti-PD-1) component. This design provides a potent initial "pulse" of CTLA-4 inhibition to prime a broad T-cell response, followed by sustained PD-1 inhibition to maintain the activity of these T-cells within the tumor microenvironment, thereby uncoupling efficacy from cumulative toxicity.
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
---|---|---|---|---|---|
2025/08/26 | Not Applicable | Not yet recruiting | |||
2025/07/29 | Not Applicable | Active, not recruiting | |||
2025/07/17 | Not Applicable | Recruiting | |||
2025/06/17 | Phase 3 | Not yet recruiting | |||
2025/06/06 | Phase 2 | Not yet recruiting | Qianfoshan Hospital | ||
2025/06/03 | Phase 3 | Not yet recruiting | |||
2025/05/13 | Phase 2 | Not yet recruiting | |||
2025/04/30 | Phase 2 | Not yet recruiting | |||
2025/04/24 | Phase 1 | Recruiting | |||
2025/04/23 | Phase 2 | Recruiting | Sun Yat-sen University |
FDA Drug Approvals
Approved Product | Manufacturer | NDC Code | Route | Strength | Effective Date |
---|---|---|---|---|---|
No FDA approvals found for this drug. |
EMA Drug Approvals
Approved Product | Authorization Holder | Status | Issued Date |
---|---|---|---|
No EMA approvals found for this drug. |
HSA Drug Approvals
Approved Product | Manufacturer | Approval Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No HSA approvals found for this drug. |
NMPA Drug Approvals
Approved Product | Company | Approval Number | Drug Type | Dosage Form | Approval Date |
---|---|---|---|---|---|
No NMPA approvals found for this drug. |
PPB Drug Approvals
Approved Product | Registration No. | Company | Licence No. | Strength | Registration Date |
---|---|---|---|---|---|
No PPB approvals found for this drug. |
TGA Drug Approvals
Approved Product | ARTG ID | Sponsor | Registration Type | Status | Registration Date |
---|---|---|---|---|---|
No TGA approvals found for this drug. |
Health Canada Drug Approvals
Approved Product | Company | DIN | Dosage Form | Strength | Market Date |
---|---|---|---|---|---|
No Health Canada approvals found for this drug. |
CIMA AEMPS Drug Approvals
Approved Product | Company | Registration Number | Pharmaceutical Form | Prescription Type | Status |
---|---|---|---|---|---|
No CIMA AEMPS (Spain) approvals found for this drug. |
Philippines FDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No Philippines FDA approvals found for this drug. |
Saudi SFDA Drug Approvals
Approved Product | Company | License Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No Saudi SFDA approvals found for this drug. |
Malaysia NPRA Drug Approvals
Approved Product | Company | Registration Number | Dosage Form | Strength | Approval Date |
---|---|---|---|---|---|
No Malaysia NPRA approvals found for this drug. |
UK EMC Drug Information
Medicine Name | MA Holder | MA Number | Pharmaceutical Form | Active Ingredient | Authorization Date |
---|---|---|---|---|---|
No UK EMC drug information found for this drug. |
Help Us Improve
Your feedback helps us provide better drug information and insights.