vTv Therapeutics Makes Significant Progress in Diabetes Treatment Trials
Exciting Developments in Diabetes Care by vTv Therapeutics
vTv Therapeutics Inc. (Nasdaq: VTVT), a pioneering biopharmaceutical company at the forefront of treating diabetes, recently announced a significant achievement in their research initiatives. The first study participant has been successfully randomized in the CATT1 Phase 3 clinical trial, which investigates cadisegliatin as an adjunctive treatment for adults with type 1 diabetes (T1D).
Understanding Cadisegliatin
Cadisegliatin is set to make waves in diabetes treatment. It's a potential first-in-class oral glucokinase activator designed to work alongside insulin, targeting the liver to improve glycemic control. The U.S. Food and Drug Administration (FDA) has recognized its potential, granting it Breakthrough Therapy designation for its innovative approach. So far, cadisegliatin has been reported to be well-tolerated in over 500 subjects during initial studies that lasted up to six months.
The Need for New Therapeutic Options
Despite technological advances in blood glucose management devices, there remains a critical need for new therapeutic options in the treatment of T1D. Currently, no FDA-approved oral adjunct therapies exist to support insulin treatment in these patients. Dr. Thomas Strack, Chief Medical Officer at vTv Therapeutics, emphasized the importance of the trial, stating, “Randomizing the first participant in CATT1 represents a significant milestone in our quest to improve glycemic control for the approximately 1.6 million Americans living with T1D.”
Details of the CATT1 Phase 3 Trial
The CATT1 trial involves a structured plan across up to 25 sites in the USA, aiming to enroll around 150 participants diagnosed with T1D. This randomized, double-blind, placebo-controlled study will assess two regimens of cadisegliatin (800 mg once or twice daily) versus a placebo in individuals currently managing their diabetes with multiple daily insulin injections or via continuous subcutaneous insulin infusion. The study will track various metrics, including the occurrence of hypoglycemic events and changes in hemoglobin A1C (HbA1c) levels, providing invaluable data on the drug's effectiveness.
Monitoring for Enhanced Safety
To further enhance participant safety, all enrollee participants will receive continuous glucose monitors (CGM). This data will be crucial, especially when monitoring level 2 and 3 hypoglycemic events, and will serve to inform the primary endpoint comparison between cadisegliatin-treated individuals and those receiving placebo.
Expert Opinions on Cadisegliatin's Potential
Experts are optimistic about the potential impact of cadisegliatin as part of diabetes therapy. Klara Klein, MD, PhD, a diabetes specialist at the University of North Carolina at Chapel Hill, noted that while advancements in medical technology have significantly improved management strategies, there are significant gaps in discovering therapies that balance glycemic control without exaggerating the risks of ketosis or hypoglycemia. Cadisegliatin stands out for its potential to not only improve overall glycemic responses but also potentially mitigate some of the mental stresses associated with managing T1D.
About vTv Therapeutics
vTv Therapeutics is committed to innovating drug candidates aimed at tackling diabetes and other chronic conditions. The company’s lead program, cadisegliatin, signifies a promising direction for the treatment of type 1 diabetes and is currently being evaluated in the CATT1 Phase 3 trial. Beyond cadisegliatin, vTv Therapeutics is advancing multiple molecules across a spectrum of chronic diseases, highlighting their commitment to pioneering research.
Contact Information
Investor Contact:
John Fraunces
LifeSci Advisors, LLC
917-355-2395
Email: jfraunces@lifesciadvisors.com
Media Contact:
Caren Begun
TellMed Strategies
201-396?8551
Email: caren.begun@tmstrat.com
Frequently Asked Questions
What is the CATT1 trial about?
The CATT1 trial is a Phase 3 clinical study to evaluate cadisegliatin as an adjunct treatment for adults with type 1 diabetes, focusing on its effects on glycemic control and safety.
What is cadisegliatin?
Cadisegliatin is a novel oral glucokinase activator designed to enhance glycemic control in individuals with type 1 diabetes.
Why is this study important?
This study addresses the lack of FDA-approved oral adjunct therapies for insulin-treated individuals with type 1 diabetes, presenting a potential breakthrough treatment.
How many participants are involved in the CATT1 trial?
Approximately 150 participants diagnosed with type 1 diabetes are expected to enroll in the trial.
What endpoints will the trial measure?
The trial will measure the incidence of hypoglycemic events as well as secondary endpoints such as hemoglobin A1C levels and time spent in the target glycemic range.
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