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Briquilimab

Generic Name
Briquilimab
Drug Type
Biotech
CAS Number
2574591-89-0
Unique Ingredient Identifier
QWX84D0DRC

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

Published: Oct 23, 2025

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/PropertyValueSource(s)
Generic NameBriquilimab1
DrugBank IDDB181361
CAS Number2574591-89-01
UNIIQWX84D0DRC1
Code DesignationsJSP191, AMG-1912
Drug TypeBiotech, Monoclonal Antibody1
Molecular Formula$C_{6426}H_{9946}N_{1718}O_{2034}S_{46}$4
Molecular Weight~145.3 kDa4

Structural and Molecular Characterization

Continue reading the full research report

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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