The next generation of RNA therapeutics

Helping the body make its own medicine.

ValamAi designs RNA therapeutics that selectively trigger a patient’s own cells to produce therapeutic proteins — exactly where they are needed most.

IND
FDA clearance for lead program VMB-100
4
Programs across urology, spine, dermatology & oncology
1 in 3
Women affected by stress urinary incontinence
$40.8B
Projected RNA therapeutics market by 2034
Why RNA

Most disease-relevant proteins are out of reach. RNA changes that.

Proteins are large, complex molecules that play a critical role in the body’s capacity to stay healthy. Most approved drugs today are small molecules or protein biologics, which can only reach a limited number of proteins or genes.

RNA therapeutics are a new class of medicines with broad applicability against disease-relevant proteins. ValamAi is building a differentiated pipeline of first-in-class RNA medicines, powered by a proprietary mRNA technology platform, to bring new options to patients with limited treatment alternatives.

How our platform works
Druggable proteome 85–90% of proteins are undruggable by classical small-molecule approaches
Reachable by small molecules Opened up by RNA therapeutics
Pipeline

First-in-class programs, advancing to the clinic.

View full pipeline
Program / Indication
DiscoveryIn vitroIn vivoIND-enablingPhase 1Phase 2Phase 3Market
VMB-100
Stress Urinary Incontinence
Engineered IGF-I mRNA · intra-urethral injection into the sphincter muscle
Stage: FDA IND cleared · Phase IIa next
FDA IND cleared
VMB-100
Disc Herniation
Engineered IGF-I mRNA · intra-disc injection
Stage: In vivo
VAI-002
Androgenetic Alopecia
Topical RNA cream
Stage: In vivo
VAI-003
Oncology
mRNA + siRNA combined in one molecule
Stage: In vitro

Partner with ValamAi

We welcome conversations about co-development, licensing and platform collaborations across urology, orthopedics, dermatology and oncology.