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Competitor Analysis: EGF-R Agonists and Antagonists

Published by: La Merie S.L.

Published: Sep. 1, 2009 - 66 Pages


Table of Contents


Index

2008 Sales of EGF-R Antagonists

EGF-R Agonists

Erbitux Pipeline

Biologics as EGF-R Antagonists

Selective EGF Receptor Antagonists

Dual EGF-R and Her2 Receptor Antagonists

Pan-ErbB (pan-Her) Receptor Antagonists

Multi-Target EGF-R Antagonists

Corporate EGF-R Agonist and Antagonist R&D Pipelines

About La Merie

Corporate EGF-R Agonist and Antagonist R&D Pipelines

Abbott

Ambit Biosciences

Amgen

Array BioPharma

AstraZeneca

Attenuon

Aveo Pharmaceuticals

Avila Therapeutics

Bharat Biotech International

Biocon

Boehringer Ingelheim

Bristol-Myers Squibb (BMD)

Celldex Therapeutics

Chugai

Curis

Daewoong Pharmaceutical Co.

Daiichi Sankyo

DxS

Eli Lilly

Genmab

GlaxoSmithKline (GSK)

GlobeImmune

Hana Biosciences

InNexus Biotechnology

ISU Abxis

Jennerex Biotherapeutics

Life Science Pharmaceuticals

Med Discovery

Medarex

Merck Serono

Micromet

Oncalis

Oncoscience

Osi Pharmaceuticals

Pfizer

Roche (& Genentech)

Scancell

Shantha Biotechnics

Shionogi

Symphogen

Takeda Pharmaceutical Co.

Transition Therapeutics

Uni-Bio Science Group

Xencor

YM Biosciences

Zenotech Laboratories

ZymoGenetics

Abstract

The present Competitive Intelligence Report about EGF-R agonists and antagonists provides a competitor evaluation in the field of epidermal growth factor receptor (EGF-R; ErbB1) targeting molecules for wound healing or treatment of cancer as of September 2009.

The human epidermal growth factor receptor (HER) family members include EGFR (erbB1), HER2/neu (erbB2), HER3 (erbB3), and HER4 (erbB4) that are structurally related, and all except HER3 contain intracellular tyrosine kinase (tk) domain. All of the HER members, except HER2, bind to extracellular ligands

EGFR, a valid target in many epithelial malignancies, is a transmembrane protein with an extracellular ligand binding domain joined to an intracellular tyrosine kinase domain. Activation of EGFR induces a cascade of downstream signaling through several pathways, such as mitogenac tivated protein kinase (MAPK) and PI3-kinase / Akt/mTOR, resulting in cellular proliferation, differentiation, survival, motility, adhesion, and repair. EGFR is overexpressed or abnormally activated in several epithelial malignancies. Several antibodies targeting EGF-R and small molecules inhibiting the EGF-R tyrosine kinase have been approved and are used for treatment of colorectal cancer, squamous cell cancer of the head & neck or pancreatic cancer, respectively. EGF-R targeting therapeutics achieved 2008 sales of US$ 3.35 bln.

The pipeline of novel EGF-R targeting molecules is rather full and includes novel antibody as well as vaccine approaches and small molecules with a broader inhibition profile. At least six next generation antibodies against EGF-R are already in clinical development and more than ten biologics are preclinical R&D including dual target antibodies or vaccines. The small molecule pipeline is focused on dual EGF-R and Her2 as well as pan-Her tk inhibitors, but also includes multi-target EGF-R tk inhibitors.

The report includes a compilation of current active projects in research and development of molecules targeting the EGF receptor. In addition, the report lists company-specific R&D pipelines of EGF-R targeting small molecules, antibodies, proteins, cells and vaccines. Competitor projects are listed in a tabular format providing information on:
  • Drug Codes,
  • Target / Mechanism of Action,
  • Class of Compound,
  • Company,
  • Product Category,
  • Indication,
  • R&D Stage and
  • additional comments with a hyperlink leading to the source of information.
Purchase of the pdf report includes a 6-month online access to the data of the report and any updates since the publication date. Access data will be sent by e-mail and allow online work with the project data to print or export an individual report.

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