Generic Name |
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---|---|---|
IND |
SNX-5422 | |
Brand Name (US) |
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Manufacturer |
Serenex | |
Drug Type |
||
Delivery |
Oral | |
Approval Status |
Discontinued | |
Indications |
||
Overall Strategy |
KIT Protein Based | |
Strategy |
Destroy KIT | |
Drug Category |
HSP90 inhibitor |
The development of SNX-5422 has been discontinued because of ocular toxicity seen in animal models and in a phase I study. Clin Cancer Res; 17(21); 1–9. ©2011 AACR.
SNX-5422 is a Heat Shock Protein 90 (Hsp90) inhibitor candidate. SNX-5422 was discovered, designed and synthesized by Serenex scientists.
According to Serenex, in pre-clinical studies, SNX-5422 has high oral bioavailability in all species tested and has demonstrated significant in vivo efficacy across a broad spectrum of tumor types.
SNX-5422 potency and tolerability exceed that of clinical compounds derived from the natural product geldanamycin (17-AAG and 17-DMAG and CNF-1010).