Data presented at Keystone Symposia on Molecular and Cellular Biology
vTv Therapeutics Inc. (Nasdaq:VTVT), a clinical-stage biopharmaceutical
company engaged in the discovery and development of new orally
administered treatments for Alzheimer’s disease and diabetes, today
announced that data from studies of its oral, small molecule GLP-1R
agonist were reported at the Keystone Symposia on G-Protein Coupled
Receptors: Structure, Signaling and Drug Discovery, held in
Keystone, CO February 21-25, 2016.
Data presented showed that TTP273, vTv’s orally bioavailable GLP-1R
agonist currently being evaluated in a Phase 2 trial, shows “functional
selectivity” for a particular subset of the full GPCR signaling
repertoire. “Functional selectivity” or “ligand bias” is an approach
used by researchers to design drugs with improved efficacy or safety
profiles. TTP273 is an allosteric standalone agonist that has
demonstrated efficacy at lowering blood glucose in humans with better
tolerability (very low incidence of nausea and vomiting), possibly
making it an improved candidate for Type 2 diabetics over current GLP-1R
analogues.
Patricia McDonald, Assistant Professor Department of Molecular
Therapeutics at The Scripps Research Institute and coauthor of this
work, stated: “GLP-1R G-protein biased ligands may offer new and
unappreciated advantages in the context of chronic treatments. Further
preclinical translational studies are ongoing to link the G-protein
biased signaling with the absence of side effects such as nausea or cell
proliferation.”
Study Details
In a poster presentation entitled, “TTP273: Oral, G-protein Pathway
Selective, Clinical-Stage GLP-1 Receptor (GLP-1R) Agonist” researchers
reported on TTP273, an orally bioavailable, small molecule GLP-1R
agonist, along with data from studies using an earlier compound, TTP054.
Current GLP-1R peptide-based agonists are available only as an
injection, and while effective in lowering blood glucose and reducing
weight, can cause serious gastrointestinal side effects in some
patients, including nausea and vomiting.
Researchers evaluated receptor signaling through G-protein and ERK
pathways, showing a relative selectivity of TTP273 for cAMP, with no
significant activation of ERK at clinically relevant concentrations,
unlike current injectable formulations. In mouse studies, TTP273
enhanced glucose-stimulated insulin secretion, decreased glucose levels
following an Oral Glucose Tolerance Test, and decreased food intake.
In a Phase 1b study in Type 2 diabetics, TTP273 was found to be safe and
well tolerated, with a low incidence of GI side effects. These results
also showed that TTP273 was effective based on glucose measurements
following a meal challenge.
vTv recently initiated the LOGRA Phase 2b study, a randomized,
double-blind, placebo-controlled, parallel group trial evaluating the
safety and efficacy of TTP273 in 156 Type 2 diabetics on stable doses of
metformin. Data from this trial are expected to be reported by the end
of 2016.
A copy of the poster will be made available in the Publications
section of the vTv website.
About Type 2 Diabetes
Type 2 diabetes is the body’s inability to properly use insulin to
control sugar in the bloodstream. It is the most common type of diabetes
(representing 90 to 95% of diabetes patients), imposing a growing burden
on healthcare systems globally. The goal of maintaining A1c levels below
7.0% is elusive for patients with this life-long disease. In addition to
unregulated glucose, diabetics commonly have a variety of
co-morbidities, including heart disease, stroke, high blood pressure,
blindness, kidney disease, amputations, dental disease, and central and
peripheral nervous system impairment.
About vTv Therapeutics Inc.
vTv Therapeutics Inc. is a clinical-stage biopharmaceutical company
engaged in the discovery and development of orally administered small
molecule drug candidates to fill significant unmet medical needs. vTv
has a pipeline of clinical drug candidates led by programs for the
treatment of Alzheimer’s disease and Type 2 diabetes as well as
treatment of inflammatory disorders and the prevention of muscle
weakness.
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