KarXT-15 Char

A startup company’s clinical program for a drug derived from an investigational therapy made by Eli Lilly & Co. announced a boost in funding Thursday.

Boston-based Karuna Pharmaceuticals said it had closed a $42 million Series A funding round, whose participants included ARCH Venture Partners, PureTech Health, the Wellcome Trust, former Third Rock Ventures partner Steven Paul and others. The company will use the money to fund a Phase II clinical trial in schizophrenia of its drug, KarXT, as well as expand its research into other therapeutic areas, like non-opiate treatments for pain.

KarXT – whose full name is Karuna-xanomeline-trospium chloride – is derived from xanomeline, originally developed by Indianapolis-based Eli Lilly and licensed by Karuna. Xanomeline is a muscarinic agonist that had shown efficacy in schizophrenia and Alzheimer’s disease, but had shown nervous system-related side effects. Xanomeline’s preclinical and clinical development history goes back more than 20 years, with PubMed listing journal articles about the drug from as far back as the early 1990s. Eli Lilly originally developed xanomeline under the company code LY246708.

Karuna’s approach is to combine the drug with trospium chloride, a muscarinic antagonist that acts only outside the brain and central nervous system. The company said that the approach of combining the agents has resulted in a clinically meaningful reduction in the aforementioned cholinergic side effects.

The company plans to start its Phase II study during this quarter, designed to replicate and expand on the efficacy and safety data that Eli Lilly had produced in its clinical trials of xanomeline.

https://medcitynews.com/2018/08/karuna-pharmaceuticals-raises-42-million-in-series-a-funding-round/

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Hope this comesout sucessfully…

Good info @firemonkey.
Thanks.

I have read about this one, it sounds promising.

"In a double-blind, placebo-controlled monotherapy trial in schizophrenia patients, a significant 24-point reduction over placebo was observed in the Positive and Negative Symptom Scale (prespecified primary endpoint), a gold standard instrument used for FDA approval. Current antipsychotic medicines typically show a 5-10 pt change over placebo in trial of this type. In a Phase II study in Alzheimer’s, xanomeline demonstrated a robust, dose-dependent reduction in behavioral symptoms (e.g., hallucinations, delusions) and provided evidence of cognitive benefit. "

This one might be available before the muscarinic drug that Vanderbilt is working on.

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