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Biotechnologies Et Génétique > Etude de marché sectorielle
 Target and Lead Validation
€ 1 400,00
Editeur :
ZZZ - Biovista
Langue :
Anglais
Date de publication :
Décembre 2000
Taille du document :
160
Autres informations :
Description , Table des matières
 
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Price : EUR 1 400,00
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Présentation de l'étude de marché - Description & Table des matières
 Target and Lead Validation

The advent of brute force approaches to lead generation has highlighted a key
 

 
bottleneck in drug development. The issue is not how many new compounds can
 

 
one make per day, but rather how many can one validate or legitimize as potential
 

 
therapeutic candidates for further development. This is the lead validation
 

 
problem of drug discovery, and whoever has technologies that can readily screen
 

 
many compounds and provide even a 70% accurate continue/discontinue prediction
 

 
will be very successful.

 

 
At present, high throughput screening, which attempts to address this issue,
 

 
is based mostly on one-to-one binding assays, where a target of interest, say
 

 
HIV protease, is exposed to potential inhibitors in a high throughput enzyme
 

 
function test. Although a priori this approach makes sense and forms the cornerstone
 

 
of current validation programs, its accuracy is fundamentally constrained by
 

 
the assumption that a good in vitro inhibitor of HIV protease in the previous
 

 
example will also arrest HIV growth in a patient setting.

 

 
The next generation of high throughput lead validation platforms may be based
 

 
on combinations of automated cellular assays, and cell-free "molecular
 

 
drug response cascades".


 

Executive Summary

Aims and Scope

IRCD Structure

PART 1: TECHNOLOGY SUMMARY

Background

The Target and Lead Validation Problem

Evolution of the Field

The Yeast Two-Hybrid System

The Impact of Genomics

State of the Art

Development Issues

Future Developments

Technology Examples

Genelabs Technologies: MERLIN ™

Acadia Pharmaceuticals: R-SAT™

Acacia Biosciences: Genome Reporter Matrixa

Genzyme Molecular Oncology: SAGE

Exelixis Pharmaceuticals: PathFindera

Genaissance Pharmaceuticals: Clasper Systema

Small Molecule Therapeutics: FISTa

PART 2: BUSINESS DEVELOPMENT

Platform Biotechnologies Current Conditions Market Size Estimates Synopsis of Notable Events in 1998-1999 (YTD)

Descriptions of Corporate Activities in 1998-1999 (YTD)

Discussion of Corporate Activities in 1998-1999 (YTD)

Mergers, Acquisitions and Spin-Out's.

Biochip Technology Access Programs

Target Identification and Validation Collaborations.

Validation of Non-Human Targets.

Target Validation and Disease Relevance.

PART 3: COMPANY DATABASE

Methodology

Concise Company Listing

Extended Company Listing

PART 4: PATENTS DATABASE

Methodology

Concise Patent Listing


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