First Participant Dosed in Europe as Cognition Therapeutics Expand Phase 2 Alzheimer's Disease Clinical Trial of Oral CT1812
December 15 2022 - 08:00AM
GlobeNewswire Inc.
Cognition Therapeutics, Inc. (Nasdaq: CGTX) (the “Company” or
“Cognition”), announced that the Phase 2 SHINE clinical trial of
CT1812, an experimental oral, once-daily capsule in development for
mild-to-moderate Alzheimer’s disease, has been expanded into
clinical sites in Spain, the Netherlands, and the Czech
Republic. CT1812 is designed to modulate a key cellular
receptor known as sigma-2 and block oligomers from binding to
neurons, thus preventing their synaptotoxic effects. This new
mechanism of action is fundamentally distinct from and
complementary with that of anti-amyloid antibody-based
immunotherapy, such as lecanemab.
The Brain Research Center Amsterdam in The Netherlands is the
first European site to enroll participants in the Phase 2 SHINE
study being conducted in approximately 144 individuals. Dr. Niels
Prins, director of the Center stated, “We are committed to offering
Alzheimer’s patients and their families access to innovative
clinical trials, such as the SHINE study of CT1812. With our
industry partners, we believe we can make inroads in development of
new medicines to slow the progression of Alzheimer’s and related
disorders.”
Anthony O. Caggiano, M.D., Ph.D., Cognition’s chief medical
officer and head of R&D added, “We believe that the approach of
targeting soluble oligomeric Aβ species has been validated by
lecanemab findings announced earlier this year by Eisai and Biogen
at CTAD 2022. However, unlike antibodies, which lower brain amyloid
levels, CT1812 was designed to shield neurons from these toxic
proteins.”
Results from initial trials with CT1812 provided evidence to
support expansion of the clinical programs. In particular, positive
trends were seen in cognition, MRI volumetric imaging and proteomic
biomarkers:
- Slower decline in ADAS-cog vs placebo over six months
- Preservation of brain volume (composite) vs placebo with
statistically significant (p<0.05) improvement in volume in
three regions of interest
- Normalization of biomarkers associated with Alzheimer’s
pathology
The SHINE study is supported by approximately $30 million in
grant funding from the National Institutes on Aging (NIA).
“We are grateful for the continued support of the NIA to
accelerate the clinical development of CT1812 and advance our
understanding of σ-2 biology in both Alzheimer’s disease and
dementia with Lewy bodies,” added Cognition president and CEO, Lisa
Ricciardi. “We appreciate the sense of urgency shown by Dr. Prins
and his colleagues at Brain Research Center Amsterdam, who worked
diligently to expedite their site activation and enroll Europe’s
first patient in the SHINE trial.”
About the SHINE StudyThe SHINE study is a
double-blind, placebo-controlled Phase 2 clinical trial designed to
enroll up to 144 participants with mild-to-moderate Alzheimer’s
disease. In addition to background therapies, participants will be
randomized to receive either placebo or one of two doses of CT1812,
taken orally daily for six months. Endpoints include safety and
biomarker evidence of disease modification as well as cognitive
function, as measured by the ADAS-Cog 11, a globally recognized
cognitive scale. More information about the SHINE study may be
found at www.shineADstudy.com. In the Netherlands, please visit
Brain Research Center.
About CT1812CT1812 is an oral small molecule
designed to penetrate the blood-brain barrier and bind selectively
to the sigma-2 (σ-2) receptor complex. The σ-2 receptor complex is
involved in the regulation of key cellular processes such as
membrane trafficking and autophagy that are damaged by toxic
interaction with Aβ oligomers, oxidative stress and other
stressors. This damage to sensitive synapses can progress to a loss
of synaptic function, which manifests as cognitive impairment and
Alzheimer’s disease progression.
CT1812 is an experimental candidate and has not been approved by
the U.S. FDA or other regulatory agency. It is currently in
development for mild-to-moderate Alzheimer’s disease in the SHINE
study (NCT03507790) and dementia with Lewy bodies in the SHIMMER
study (NCT05225415).About Cognition Therapeutics,
Inc.Cognition Therapeutics, Inc. is a clinical-stage
biopharmaceutical company engaged in the discovery and development
of innovative, small molecule therapeutics targeting age-related
degenerative disorders of the central nervous system and retina. We
are currently investigating our lead candidate CT1812 in clinical
programs in Alzheimer’s disease, dementia with Lewy bodies (DLB)
and dry age-related macular degeneration (dry AMD). We believe
CT1812 and our pipeline of σ-2 receptor modulators can regulate
pathways that are impaired in these diseases. We believe that
targeting the σ-2 receptor with CT1812 represents a mechanism
functionally distinct from other current approaches in clinical
development for the treatment of degenerative diseases. More about
Cognition Therapeutics and its pipeline can be found
at https://cogrx.com.
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Contact Information: Cognition
Therapeutics, Inc. info@cogrx.com
Aline Sherwood (media) Scienta
Communications asherwood@scientapr.com Daniel
Kontoh-Boateng/Rosalyn Christian (investors) Tiberend
Strategic Advisors, Inc. dboateng@tiberend.com
rchristian@tiberend.com
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