MedPath

LNL-005

Generic Name
LNL-005

Overview

No overview information available.

Indication

No indication information available.

Associated Conditions

No associated conditions information available.

Research Report

Published: May 13, 2025

LNL-005 Report

Name: LNL-005 Name (English): LNL-005

Drug Type: Bispecific antibody

Synonyms: BIS5, LB1410

Target: PD-1 x TIM3

Action: Inhibitor

Mechanism of Action: LNL-005 is a bispecific antibody that simultaneously targets Programmed cell death protein 1 (PD-1) and Hepatitis A virus cellular receptor 2 (TIM3). By blocking both PD-1 and TIM3 pathways, LNL-005 aims to enhance the immune response against cancer cells, particularly in patients resistant or refractory to PD-1/PD-L1 inhibitor treatments. This dual blockade can improve T cell activation and function, as well as modulate the activity of other immune cells like NK cells and dendritic cells.

Therapeutic Areas:

  • Neoplasms (Cancer)
  • Immune System Diseases
  • Digestive System Disorders

Active Indication:

  • Metastatic Solid Tumor
  • Advanced cancer
  • Advanced Malignant Solid Neoplasm

Inactive Indication: Not specified.

Highest Phase of Development: Phase I

Countries/Locations of Clinical Trials:

  • China
  • United States

Mechanism of Action Details: LNL-005 is engineered with two distinct antigen-binding fragments (Fabs), one for PD-1 and one for TIM3. This allows it to simultaneously bind to both targets on immune cells and tumor cells. By doing so, it disrupts the immunosuppressive signals mediated by these checkpoint proteins, leading to increased anti-tumor immunity.

Clinical Trial Information: A Phase I, multicenter, open-label study (NCT05357651) is ongoing in patients with advanced and/or metastatic solid tumors in China to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, immunogenicity, and preliminary efficacy of LNL-005.

Continue reading the full research report

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.

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.