FragPhore™ PLATFORM
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Unique and proprietary small fragment molecules
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Modules to improve drug-like & pharmaceutical properties
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Allows rapid med chem lead generation & optimization
While withdrawal or failure of clinical drug candidates can be attributed to multiple reasons including: commercial/market considerations, intolerable side effects, or lack of efficacy, the majority of clinical drug candidates fail due to unsuitable pharmaceutical properties (e.g.: ADME, PK, solubility, etc.). Recent strategic changes in the drug discovery paradigm incorporating early assessment of lead molecule pharmaceutical properties and concomitant development of both structure-activity-relationships (SAR) and structure-property-relationships (SPR) in advancing leads are formulated to effectively address these property-related failure rates.
At Hager, we have strategies to deploy our unique and proprietary small molecule Fragment Pharmacophores, FragPhore™, to generate pre-clinical lead candidates endowed with desirable drug-like physical properties such as:
The unique FragPhore™ library compounds are individually designed and can feature a variety of functional groups which allow facile and efficient modular adaptation of these moieties into core molecules developed from new or existing SAR / SPR campaigns. The utility for these drug-like fragment molecules is multi-faceted and includes:
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improvement of physico-chemical profile of emerging leads
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rapid identification of new medicinal chemistry leads and SAR expansion
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enhancement of intellectual property and patent landscape
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access to novel, clinically-validated drug-space for use in fast-follower or drug rescue strategies
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potentially fewer SAR cycle iterations
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risk mitigation
To best meet the needs of our clients and partners, access to the Hager FragPhore™ molecules may be accomplished on either an exclusive or non-exclusive basis. To find out additional information on the Hager FragPhore™ Platform and to see firsthand how this approach can impact on your discovery goals, please contact us.