Promising new drug development could help treat cachexia
University of Missouri News Apr 27, 2017
Researchers at the University of Missouri in partnership with Tensive Controls, Inc. have developed a drug that could reverse cachexia. The team currently is seeking canine candidates for a pilot study to test the new drug.
ÂThe goal of this drug trial is to extend and improve the quality of life of cancer patients who are suffering from cachexia, said Sandra Bechtel, associate professor of medical oncology at the MU Veterinary Health Center and principal investigator for the drug clinical trial. ÂThe clinical trial is targeting a disease that significantly decreases quality of life. We are working to improve end–stage quality of life for our veterinary patients with the hopes of translating the improvements to human patients.Â
Cachexia is caused by inflammatory cytokines, or small proteins that when released have an effect on the behavior of the cells around them. Certain cytokines in the brain cause the body to be hyperactive, decreasing appetite and causing weight loss in individuals with cachexia.
Kenneth A. Gruber, principal investigator at the MU Dalton Cardiovascular Research Center and president and founder of Tensive Controls, Inc., and his team have developed a drug that is able to cross the blood brain barrier, a protective barrier that typically prevents drugs, toxins or microbes from entering the brain, and inhibits overstimulation of the melanocortin system. The drug is administered via a subcutaneous, below the skin, injection.
ÂPreliminary results of the trial are promising, said Gruber, who also holds an appointment as a professor of pharmacology and physiology in the MU School of Medicine. ÂThree dogs have already received the drug therapy and have gained an average of 7.5 percent of their body weight back over a 28–day trial. Dogs who have taken the drug for longer periods of time have improved to ideal body condition.Â
The early–stage results of this research are promising. If additional studies are successful within the next few years, MU and Tensive Controls officials will request authority from the federal government to begin human drug development (this is commonly referred to as the Âinvestigative new drug status). After this status has been granted, researchers may conduct human clinical trials with the hope of developing new treatments for cancer cachexia in people.
The startup company associated with this research, Tensive Controls, Inc., highlights the universityÂs impact on the stateÂs economic development efforts, including commercialization of research conducted at Mizzou, workforce development and job growth, quality of life improvements for residents, and attracting corporations and businesses to the state. During the past five years, companies commercializing MU technologies have secured hundreds of millions of dollars in investments and grants to advance their commercialization efforts. In 2016, the Office of Technology Management and Industry Relations reported that Mizzou received $14.9 million in revenue from more than 40 technology licenses.
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ÂThe goal of this drug trial is to extend and improve the quality of life of cancer patients who are suffering from cachexia, said Sandra Bechtel, associate professor of medical oncology at the MU Veterinary Health Center and principal investigator for the drug clinical trial. ÂThe clinical trial is targeting a disease that significantly decreases quality of life. We are working to improve end–stage quality of life for our veterinary patients with the hopes of translating the improvements to human patients.Â
Cachexia is caused by inflammatory cytokines, or small proteins that when released have an effect on the behavior of the cells around them. Certain cytokines in the brain cause the body to be hyperactive, decreasing appetite and causing weight loss in individuals with cachexia.
Kenneth A. Gruber, principal investigator at the MU Dalton Cardiovascular Research Center and president and founder of Tensive Controls, Inc., and his team have developed a drug that is able to cross the blood brain barrier, a protective barrier that typically prevents drugs, toxins or microbes from entering the brain, and inhibits overstimulation of the melanocortin system. The drug is administered via a subcutaneous, below the skin, injection.
ÂPreliminary results of the trial are promising, said Gruber, who also holds an appointment as a professor of pharmacology and physiology in the MU School of Medicine. ÂThree dogs have already received the drug therapy and have gained an average of 7.5 percent of their body weight back over a 28–day trial. Dogs who have taken the drug for longer periods of time have improved to ideal body condition.Â
The early–stage results of this research are promising. If additional studies are successful within the next few years, MU and Tensive Controls officials will request authority from the federal government to begin human drug development (this is commonly referred to as the Âinvestigative new drug status). After this status has been granted, researchers may conduct human clinical trials with the hope of developing new treatments for cancer cachexia in people.
The startup company associated with this research, Tensive Controls, Inc., highlights the universityÂs impact on the stateÂs economic development efforts, including commercialization of research conducted at Mizzou, workforce development and job growth, quality of life improvements for residents, and attracting corporations and businesses to the state. During the past five years, companies commercializing MU technologies have secured hundreds of millions of dollars in investments and grants to advance their commercialization efforts. In 2016, the Office of Technology Management and Industry Relations reported that Mizzou received $14.9 million in revenue from more than 40 technology licenses.
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