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Indiana University School of Medicine

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Indianapolis, Indiana 46202

Global Leader in Alzheimer's Disease

Global Leader in Dementia

Conducts research for Chronic Kidney Disease

Conducts research for Nonalcoholic Steatohepatitis

Conducts research for Type 2 Diabetes

232 reported clinical trials

27 medical researchers

Photo of Indiana University School of Medicine in IndianapolisPhoto of Indiana University School of Medicine in IndianapolisPhoto of Indiana University School of Medicine in Indianapolis

Summary

Indiana University School of Medicine is a medical facility located in Indianapolis, Indiana. This center is recognized for care of Alzheimer's Disease, Dementia, Chronic Kidney Disease, Nonalcoholic Steatohepatitis, Type 2 Diabetes and other specialties. Indiana University School of Medicine is involved with conducting 232 clinical trials across 436 conditions. There are 27 research doctors associated with this hospital, such as Monika Fischer, Jared Brosch, Raj Vuppalanchi, MD, and Linda DiMeglio, MD.

Area of expertise

1

Alzheimer's Disease

Global Leader

Indiana University School of Medicine has run 30 trials for Alzheimer's Disease. Some of their research focus areas include:

PSEN2 positive
PSEN1 positive
APP positive
2

Dementia

Global Leader

Indiana University School of Medicine has run 13 trials for Dementia. Some of their research focus areas include:

PSEN2 positive
PSEN1 positive
APP positive

Top PIs

Clinical Trials running at Indiana University School of Medicine

Alzheimer's Disease

Dementia

Prostate Cancer

Sickle Cell Disease

Phenylketonuria

Bladder Cancer

Rheumatoid Arthritis

Aortic Dissection

Post-Traumatic Stress Disorder

Kidney Failure

Image of trial facility.

Gantenerumab

for Alzheimer's Disease

The purpose is to evaluate the biomarker effect, safety, and tolerability of investigational study drugs in participants who are known to have an Alzheimer's disease (AD)-causing mutation. Stage 1 will determine if treatment with the study drug prevents or slows the rate of amyloid beta (Aβ) pathological disease accumulation demonstrated by Aβ positron emission tomography (PET) imaging. Stage 2 will evaluate the effect of early Aβ plaque reduction/prevention on disease progression by assessing downstream non-Aβ biomarkers of AD (e.g., CSF total tau, p-tau, NfL) compared to an external control group from the DIAN-OBS natural history study and the DIAN-TU-001 placebo-treated participants.

Recruiting

0 awards

Phase 2 & 3

10 criteria

Image of trial facility.

LY3954068

for Alzheimer's Disease

The main purpose of this study is to evaluate the safety of LY3954068 in participants with early symptomatic Alzheimer's Disease (AD). The study will also investigate how much LY3954068 gets into the bloodstream and will test the effects of LY3954068 on markers of AD. The study will be comprised of two parts, A and B. Each enrolled participant in Part A will receive a single dose of LY3954068 or placebo (no active drug) given into the spinal fluid. Each participant in Part B will receive 2 doses of either LY3954068 or placebo administered into the spinal fluid. Participants will have the opportunity to join an optional bridging period to a separate potential study where participants would receive LY3954068. The study will last up to approximately 45 weeks for Part A, and 100 weeks for Part B, including the screening period.

Recruiting

0 awards

Phase 1

Image of trial facility.

Remternetug

for Alzheimer's Disease

The purpose of this research study is to test the study drug, referred to as remternetug, to determine its effectiveness for the study treatment of asymptomatic (at risk) Alzheimer disease in individuals with AD-causing mutations. This study will also investigate the effects of remternetug on biomarkers (measures of the disease including brain scans, blood and spinal fluid tests), examine safety data to identify any potential benefits or risks, and examine how well participants can tolerate remternetug. Stage 1 will determine if treatment with the study drug prevents or reverses amyloid beta (Aβ) accumulation compared with placebo in participants with dominantly inherited Alzheimer's disease (DIAD). Stage 2 will evaluate the effect of early anti-amyloid treatment on downstream biomarkers of AD in treated participants compared to external control groups.

Recruiting

0 awards

Phase 2 & 3

2 criteria

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Frequently asked questions

What kind of research happens at Indiana University School of Medicine?

Unbiased Results

We believe in providing patients with all the options.

Your Data Stays Your Data

We only share your information with the clinical trials you're trying to access.

Verified Trials Only

All of our trials are run by licensed doctors, researchers, and healthcare companies.

Terms of Service·Privacy Policy·Cookies·Security

Unbiased Results

We believe in providing patients with all the options.

Your Data Stays Your Data

We only share your information with the clinical trials you're trying to access.

Verified Trials Only

All of our trials are run by licensed doctors, researchers, and healthcare companies.

Terms of Service·Privacy Policy·Cookies·Security