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LAG-3 Antagonist - Pipeline Insight, 2021

  • ID: 5262044
  • Clinical Trials
  • February 2021
  • Region: Global
  • 70 pages
  • DelveInsight

FEATURED COMPANIES

  • Abeome Corporation
  • Avacta
  • Bristol-Myers Squibb
  • Crescendo Biologics
  • F-star Therapeutics
  • MacroGenics
This “LAG-3 Antagonist - Pipeline Insight, 2021,” report provides comprehensive insights about 20+ companies and 20+ pipeline drugs in LAG-3 Antagonist pipeline landscape. It covers the pipeline drug profiles, including clinical and nonclinical stage products. It also covers the therapeutics assessment by product type, stage, route of administration, and molecule type. It further highlights the inactive pipeline products in this space.

Geography Covered
  • Global coverage
LAG-3 Antagonist Understanding

LAG-3 Antagonist: Overview

LAG-3 is Lymphocyte Activation Gene-3 (LAG-3 or CD223) is a cell surface molecule expressed on activated T cells, NK cells, B cells, and plasmacytoid dendritic cells. It is involved in the regulation of the immune system. LAG3 was discovered by Triebel and colleagues in 1990 as a novel 498-amino acid type I transmembrane protein. Under physiological conditions, LAG3 is an activation marker for CD4+ and CD8+ T cells. LAG-3 plays an important role in modulating T cell expansion and function, and blockade of LAG-3 with monoclonal antibodies can augment T cell function in multiple models. Lymphocyte Activation Gene-3 is a potential cancer immunotherapeutic target due to its negative regulatory role on T cells and its capacity, in combination with PD1, to mediate a state of exhaustion. Several LAG3 modulating immunotherapeutics are currently in various stages of clinical and pre-clinical development.

Report Highlights
  • The companies and academics are working to assess challenges and seek opportunities that could influence LAG-3 Antagonist R&D. The therapies under development are focused on novel approaches for LAG-3 Antagonist.
  • On 5th May 2020 Crescendo Biologics and Cancer Research announced a Clinical Development Partnership to progress one of Crescendo’s novel bispecific Humabody® immunotherapies, CB213, into clinical trials targeting cancers of high unmet medical need. Under the terms of the agreement, Cancer Research UK’s Centre for Drug Development will sponsor and fund a future Phase I clinical trial for CB213, in patients with solid tumors.
LAG-3 Antagonist Emerging Drugs Chapters

This segment of the LAG-3 Antagonist report encloses its detailed analysis of various drugs in different stages of clinical development, including phase III, II, I, preclinical and Discovery. It also helps to understand clinical trial details, expressive pharmacological action, agreements and collaborations, and the latest news and press releases.

LAG-3 Antagonist Emerging Drugs
  • Tebotelimab: MacroGenics
Tebotelimab (previously known as MGD013) is an investigational, first-in-class bispecific, tetravalent DART molecule targeting PD-1 and LAG-3. Tebotelimab has been engineered to bind PD-1 and LAG-3 concomitantly or independently and disrupt these non-redundant inhibitory pathways to further restore exhausted T-cell function.
  • LAG525: Novartis
LAG525, also known as IMP701 is an investigational molecule being developed to potentially treat a range of solid tumors. It is a high-affinity, ligand-blocking, humanized anti-LAG-3 IgG4 antibody which blocks the binding of the known LAG-3 ligand MHC class II to LAG-3. Immutep began the development of LAG525 and is now being continued by Novartis in collaboration with the Australian biotechnology company Prima BioMed.

LAG-3 Antagonist: Therapeutic Assessment

This segment of the report provides insights about the different LAG-3 Antagonist drugs segregated based on following parameters that define the scope of the report, such as:

Major Players working on LAG-3 Antagonist

There are approx. 20+ key companies which are developing the LAG-3 Antagonist. The companies which have their LAG-3 Antagonist drug candidates in the most advanced stage, i.e. Phase II/III include, Bristol-Myers Squibb/Ono Pharmaceuticals.

The report covers around 20+ products under different phases of clinical development like
  • Late-stage products (Phase III and
  • Mid-stage products (Phase II and
  • Early-stage products (Phase I/II and Phase I) along with the details of
  • Pre-clinical and Discovery stage candidates
  • Discontinued & Inactive candidates
  • Route of Administration
LAG-3 Antagonist pipeline report provides the therapeutic assessment of the pipeline drugs by the Route of Administration. Products have been categorized under various ROAs such as
  • Infusion
  • Intradermal
  • Intramuscular
  • Intranasal
  • Intravaginal
  • Oral
  • Parenteral
  • Subcutaneous
  • Topical
  • Molecule Type
Products have been categorized under various Molecule types such as
  • Vaccines
  • Monoclonal Antibody
  • Peptides
  • Polymer
  • Small molecule
  • Product Type
The drugs have been categorized under various product types like Mono, Combination and Mono/Combination.

LAG-3 Antagonist: Pipeline Development Activities

The report provides insights into different therapeutic candidates in phase III, II, I, preclinical and discovery stage. It also analyses LAG-3 Antagonist therapeutic drugs key players involved in developing key drugs.

Pipeline Development Activities

The report covers the detailed information of collaborations, acquisition and merger, licensing along with a thorough therapeutic assessment of emerging LAG-3 Antagonist drugs.

LAG-3 Antagonist Report Insights
  • LAG-3 Antagonist Pipeline Analysis
  • Therapeutic Assessment
  • Unmet Needs
  • Impact of Drugs
LAG-3 Antagonist Report Assessment
  • Pipeline Product Profiles
  • Therapeutic Assessment
  • Pipeline Assessment
  • Inactive drugs assessment
  • Unmet Needs
Key Questions Answered

Current Scenario and Emerging Therapies:
  • How many companies are developing LAG-3 Antagonist drugs?
  • How many LAG-3 Antagonist drugs are developed by each company?
  • How many emerging drugs are in mid-stage, and late-stage of development for LAG-3 Antagonist?
  • What are the key collaborations (Industry-Industry, Industry-Academia), Mergers and acquisitions, licensing activities related to the LAG-3 Antagonist therapeutics?
  • What are the recent trends, drug types and novel technologies developed to overcome the limitation of existing therapies?
  • What are the clinical studies going on for LAG-3 Antagonist and their status?
  • What are the key designations that have been granted to the emerging drugs?
Key Players
  • MacroGenics
  • Novartis
  • Merck Sharp & Dohme
  • Crescendo Biologics
  • F-star Therapeutics
  • MICROBIO Group
  • Bristol-Myers Squibb
  • Ono Pharmaceuticals
  • Symphogen
  • Avacta
  • Abeome Corporation
Key Products
  • Tebotelimab
  • LAG525
  • Favezelimab
  • CB213
  • FS-118
  • SNA-03
  • Relatlimab
  • Sym022
  • AVA-0017
  • LAG3 antagonist
Note: Product cover images may vary from those shown

FEATURED COMPANIES

  • Abeome Corporation
  • Avacta
  • Bristol-Myers Squibb
  • Crescendo Biologics
  • F-star Therapeutics
  • MacroGenics
Introduction

Executive Summary

LAG-3 Antagonist: Overview
  • Structure
  • Mechanism of Action
Pipeline Therapeutics
  • Comparative Analysis
Therapeutic Assessment
  • Assessment by Product Type
  • Assessment by Stage and Product Type
  • Assessment by Route of Administration
  • Assessment by Stage and Route of Administration
  • Assessment by Molecule Type
  • Assessment by Stage and Molecule Type
LAG-3 Antagonist - Analytical Perspective

In-depth Commercial Assessment
  • LAG-3 Antagonist companies' collaborations, Licensing, Acquisition - Deal Value Trends
LAG-3 Antagonist Collaboration Deals
  • Company-Company Collaborations (Licensing / Partnering) Analysis
  • Company-University Collaborations (Licensing / Partnering) Analysis
Late Stage Products (Phase III)
  • Comparative Analysis
Drug name: Company name
  • Product Description
  • Research and Development
  • Product Development Activities
Mid Stage Products (Phase II)
  • Comparative Analysis
Tebotelimab: MacroGenics
  • Product Description
  • Research and Development
  • Product Development Activities
Early Stage Products (Phase I)
  • Comparative Analysis
FS-118: F-star Therapeutics
  • Product Description
  • Research and Development
  • Product Development Activities
Pre-clinical and Discovery Stage Products
  • Comparative Analysis
CB213: Crescendo Biologics
  • Product Description
  • Research and Development
  • Product Development Activities
Inactive Products
  • Comparative Analysis
LAG-3 Antagonist Key Companies

LAG-3 Antagonist Key Products

LAG-3 Antagonist - Unmet Needs

LAG-3 Antagonist - Market Drivers and Barriers

LAG-3 Antagonist - Future Perspectives and Conclusion

LAG-3 Antagonist Analyst Views

LAG-3 Antagonist Key Companies

Appendix

List of Tables
Table 1 Total Products for LAG-3 Antagonist
Table 2 Late Stage Products
Table 3 Mid Stage Products
Table 4 Early Stage Products
Table 5 Pre-clinical & Discovery Stage Products
Table 6 Assessment by Product Type
Table 7 Assessment by Stage and Product Type
Table 8 Assessment by Route of Administration
Table 9 Assessment by Stage and Route of Administration
Table 10 Assessment by Molecule Type
Table 11 Assessment by Stage and Molecule Type
Table 12 Inactive Products

List of Figures
Figure 1 Total Products for LAG-3 Antagonist
Figure 2 Late Stage Products
Figure 3 Mid Stage Products
Figure 4 Early Stage Products
Figure 5 Preclinical and Discovery Stage Products
Figure 6 Assessment by Product Type
Figure 7 Assessment by Stage and Product Type
Figure 8 Assessment by Route of Administration
Figure 9 Assessment by Stage and Route of Administration
Figure 10 Assessment by Molecule Type
Figure 11 Assessment by Stage and Molecule Type
Figure 12 Inactive Products
Note: Product cover images may vary from those shown
  • MacroGenics
  • Novartis
  • Merck Sharp & Dohme
  • Crescendo Biologics
  • F-star Therapeutics
  • MICROBIO Group
  • Bristol-Myers Squibb
  • Ono Pharmaceuticals
  • Symphogen
  • Avacta
  • Abeome Corporation
Note: Product cover images may vary from those shown
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