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Delta Research Partners

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Monroe, Louisiana 71201

Global Leader in Ulcerative Colitis

Global Leader in Colitis

Conducts research for Colorectal Cancer

Conducts research for Nonalcoholic Steatohepatitis

Conducts research for Non-alcoholic Fatty Liver Disease

51 reported clinical trials

4 medical researchers

Photo of Delta Research Partners in MonroePhoto of Delta Research Partners in MonroePhoto of Delta Research Partners in Monroe

Summary

Delta Research Partners is a medical facility located in Monroe, Louisiana. This center is recognized for care of Ulcerative Colitis, Colitis, Colorectal Cancer, Nonalcoholic Steatohepatitis, Non-alcoholic Fatty Liver Disease and other specialties. Delta Research Partners is involved with conducting 51 clinical trials across 56 conditions. There are 4 research doctors associated with this hospital, such as Bal Raj Bhandari, Henry Hill Hinkle, III, Henry Hill Hinkle III, and Henry Hinkle III, MD.

Top PIs

Clinical Trials running at Delta Research Partners

Liver Fibrosis

Fatty Liver Disease

Image of trial facility.

Survodutide

for Fatty Liver Disease

This study is open to adults who are at least 18 years old living with obesity and have: * a confirmed liver disease called non-alcoholic steatohepatitis (NASH)/metabolic associated steatohepatitis (MASH) and * moderate or advanced liver fibrosis People with a history of acute or chronic liver diseases other than MASH or chronic alcohol intake cannot take part in this study. The purpose of this study is to find out whether a medicine called survodutide helps people with MASH and moderate or advanced liver fibrosis improve their liver function. This study has 2 parts. The purpose of the first part of this study is to find out the effect of survodutide on MASH and liver fibrosis. The purpose of the second part is to find out how safe and effective survodutide is in improving liver function. Participants are put into 2 groups randomly, which means by chance. 1 group gets survodutide and 1 group gets placebo. Placebo looks like survodutide but does not contain any medicine. Each participant has twice the chance of getting survodutide. Participants and doctors do not know who is in which group. Participants inject survodutide or placebo under their skin once a week. The survodutide doses are slowly increased until the target dose is reached. All participants receive counselling to make changes to their diet and to exercise regularly. Participants are in the study for up to 7 years. During this time, they regularly visit the study site or have remote visits by video call. For about the first year of the study, participants have these visits every 2 weeks, increasing to every 4 weeks and then every 6 weeks. After being in the study for a little over a year participants will then alternate between visiting the study site or having a remote visit every 3 months until the end of the study. The doctors check participants' health and take note of any unwanted effects. The participants' body weight and effects on the stomach and intestines are regularly measured. At some visits the liver is measured using different imaging methods. At 2 or 3 visits doctors take a small sample of liver tissue (biopsy). The participants also fill in questionnaires about their symptoms and quality of life. The results are compared between the groups to see whether the treatment works.

Recruiting

1 award

Phase 3

1 criteria

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Frequently asked questions

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