Lead Programs

ProgramsIndicationDiscoveryLead OptimizationIND-EnablingPartner
STAT3 SH2 domain
STAT3 SH2 domain Inflammatory Diseases

Wholly-owned
STAT3 SH2 domain Cancer

Wholly-owned
STAT6 SH2 domain
STAT6 SH2 domain Inflammatory Diseases

1
STAT6 SH2 domain Cancer

Undisclosed SH2 domain
Undisclosed SH2 domain Inflammatory Diseases

Wholly-owned
Undisclosed SH2 domain Cancer

Wholly-owned
Undisclosed Non-SH2 domain
Undisclosed SH2 domain Cancer

Wholly-owned
Undisclosed Non-SH2 domain Cancer

Wholly-owned
ProgramIndicationStagePartner
STAT3 SH2 domain
STAT3 SH2 domain Inflammatory DiseasesIND-EnablingWholly-owned
STAT3 SH2 domain CancerIND-EnablingWholly-owned
STAT6 SH2 domain
STAT6 SH2 domain Inflammatory DiseasesIND-Enabling1
STAT6 SH2 domain CancerIND-Enabling
Undisclosed SH2 domain
Undisclosed SH2 domain Inflammatory DiseasesDiscoveryWholly-owned
Undisclosed SH2 domain CancerDiscoveryWholly-owned
Undisclosed Non-SH2 domain
Undisclosed SH2 domain CancerDiscoveryWholly-owned
Undisclosed Non-SH2 domain CancerDiscoveryWholly-owned

1Recludix has the option to participate in an equal profit-sharing arrangement in the US, which includes certain co-promotion activities

STAT Inhibitors

Recludix is pursuing a novel approach to modulate the activity of the JAK/STAT family of pathways by targeting the downstream STAT proteins through inhibition of their SH2 domains. Targeting individual STAT proteins with highly selective inhibitors is expected to provide a more focused biological response than is observed with many JAK family kinase inhibitors. This may result in fewer side effects and the ability to more profoundly inhibit a specific pathway, even in cancer, at well-tolerated doses.

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New Target Opportunities Identified with Platform

The opportunity to identify inhibitors of new targets with Recludix’s platform is vast. There are 120 SH2 domains identified in humans, and many targets that are known to play a role in disease pathology have SH2 domains. Additionally, the distinct features of Recludix’s integrated technology platform can be used to drug non-SH2 domain targets.