Overview
Briquilimab is a humanized aglycosylated IgG1 kappa monoclonal antibody targeting CD117 (cKit).
Indication
No indication information available.
Associated Conditions
No associated conditions information available.
Research Report
Briquilimab (JSP191): A Comprehensive Monograph on a Novel Anti-CD117 Monoclonal Antibody
Drug Identification and Physicochemical Properties
Nomenclature and Identifiers
Briquilimab is an investigational biotech therapeutic classified as a protein-based therapy, specifically a monoclonal antibody (mAb).[1] Its development and identification are tracked through a series of standardized nomenclature and registry numbers essential for regulatory, clinical, and research purposes. The generic name assigned to the molecule is Briquilimab.[1] The drug is cataloged in the DrugBank database under the accession number DB18136.[1]
Throughout its development history, Briquilimab has been known by several code designations and synonyms. It was initially developed under the code name AMG 191 (also styled as AMG-191 or AMG191).[1] Following its acquisition and further development by Jasper Therapeutics, it became widely known as JSP191 (also JSP 191 or JSP-191).[1] It is also referred to functionally as an anti-c-Kit monoclonal antibody.[2] These synonyms are critical for tracing the molecule's progression through preclinical and clinical stages across different sponsoring organizations.
For chemical and substance registration, Briquilimab is assigned the Chemical Abstracts Service (CAS) Number 2574591-89-0 and the Unique Ingredient Identifier (UNII) QWX84D0DRC.[1] A summary of these key identifiers is provided in Table 1.
Table 1: Key Identifiers and Properties of Briquilimab
| Identifier/Property | Value | Source(s) |
|---|---|---|
| Generic Name | Briquilimab | 1 |
| DrugBank ID | DB18136 | 1 |
| CAS Number | 2574591-89-0 | 1 |
| UNII | QWX84D0DRC | 1 |
| Code Designations | JSP191, AMG-191 | 2 |
| Drug Type | Biotech, Monoclonal Antibody | 1 |
| Molecular Formula | $C_{6426}H_{9946}N_{1718}O_{2034}S_{46}$ | 4 |
| Molecular Weight | ~145.3 kDa | 4 |
Structural and Molecular Characterization
Clinical Trials
Title | Posted | Study ID | Phase | Status | Sponsor |
|---|---|---|---|---|---|
2024/12/16 | Phase 2 | ENROLLING_BY_INVITATION | |||
2024/09/19 | Phase 1 | Terminated | |||
2024/04/09 | Phase 1 | Terminated | |||
2023/12/08 | Phase 1 | Recruiting | |||
2023/06/18 | Phase 2 | Active, not recruiting | |||
2023/06/15 | Phase 1 | Terminated | |||
2022/11/01 | Early Phase 1 | Active, not recruiting | |||
2022/05/03 | Phase 1 | Active, not recruiting | |||
2021/03/05 | Phase 1 | Recruiting | Porteus, Matthew, MD |
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. | |||||
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