Neumora Therapeutics IPO Presentation Deck
NMRA-511: V1aR Antagonist Broad Potential Across Neuropsychiatric Disorders
Pharmacology
Antagonist of vasopressin 1a receptor (V1aR),
with high selectivity over V1b, V2 (greater than
3,000-fold) and oxytocin receptors
(approximately 300-fold)
Vasopressin plays a role in the regulation of
aggression, affiliation, stress and anxiety
response
Indication
Agitation in Alzheimer's disease
Status
Conducting Phase 1 Multiple Ascending Dose
(MAD) study in human healthy volunteers
Drug Profile
Oral, once-daily
Strong IP Protection
Expect exclusivity through 2042+, based on
composition of matter protection and estimated
patent term extension
Strong Biologic Activity
Demonstrated
NMRA-511 reduced
measures of anxiety in an
NHP preclinical model, with
a corresponding EEG
signature in Phase 1
V1aR EXPRESSION
HPC-O
CeA-
ECM
-Lateral
Neuron
cytoplasm
septum
Expressed in multiple
brain regions
-BNST
-A/LHy
V1aR
Gq/11
Endogenous pathways
Enhanced in disease
Drug impact
Antagonist
of V1aR
PLC signaling
cascade
IP₁
DAG
NMRA-511
The vasopressin system acting
through V1aR modulates anxiety and
threat-related behaviors, aggression
and social-emotional processing
Increased
intracellular
Ca2+
PKC
PKC activation
and translocation
to membrane
Confidential
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