Kayothera is advancing first-in-class oral small molecules across cardiometabolic disease, obesity, and reproductive health.
Pipeline
Pipeline command center
Three programs connected by one upstream biological foundation.
Program selector03 active programs
Development pathwayPreclinical focus
Current development focus
KAYO-1732
Designed to inhibit retinoid synthesis in tissues relevant to type 2 diabetes and cardiometabolic disease, with a development focus on beta-cell function and metabolic health.
Disease area
Type 2 diabetes / cardiometabolic disease
Supporting science
ALDH1a3 biology, pancreatic beta-cell function, adipose tissue and vasculature.
Designed to inhibit ALDH1a2-mediated retinoic acid synthesis in reproductive biology, with relevance to spermatogenesis and male contraceptive development.
Disease area
Male contraceptive / reproductive health
Supporting science
ALDH1a2, retinoic acid synthesis, Sertoli cells, and spermatogenesis.
KAYO-1609Male contraception / reproductive healthIND-enabling / toward IND
Target ID
In Vitro
In Vivo POC
DDC
IND-enabling
IND
Phase 1
Relative progress reflects Kayothera’s original Science-page pipeline chart and remains subject to client confirmation, study outcomes, regulatory feedback, funding, and company strategy.
Program details
Development priorities
Program descriptions reflect current public positioning. Exact future stages and timing remain subject to study outcomes and company strategy.
01KAYO-1732
Type 2 diabetes / cardiometabolic disease
Retinoid synthesis / ALDH1a3-related biology
Designed to inhibit retinoid synthesis in tissues relevant to type 2 diabetes and cardiometabolic disease, with a development focus on beta-cell function and metabolic health.
Development candidate nominated for type 2 diabetes and cardiometabolic indications.
Supporting science
ALDH1a3 biology, pancreatic beta-cell function, adipose tissue and vasculature.
Planned next milestone
Preclinical development priorities
02KAYO-2000
Obesity
Rexinoid pathway / ALDH1a1-related biology
Designed to target rexinoid pathway biology tied to thyroid function, mitochondrial function, adipogenesis, and energy expenditure.
Advancing an oral small-molecule approach for obesity-related pathway biology.
Supporting science
Rexinoid signaling, thyroid and mitochondrial function, and energy expenditure.
Planned next milestone
Lead program development priorities
03KAYO-1609
Male contraceptive / reproductive health
ALDH1a2 / retinoic acid synthesis / Sertoli cells
Designed to inhibit ALDH1a2-mediated retinoic acid synthesis in reproductive biology, with relevance to spermatogenesis and male contraceptive development.
Exploring pathway-selective inhibition in reproductive health.
Supporting science
ALDH1a2, retinoic acid synthesis, Sertoli cells, and spermatogenesis.