Health Research
and Clinical Studies

All IN for Health provides a list of hundreds of active health studies happening right here in Indiana. These health studies are conducted by faculty at Indiana University, Purdue University, and the University of Notre Dame.

All IN for Health provides a list of hundreds of active health studies happening right here in Indiana. These health studies are conducted by faculty at Indiana University, Purdue University, and the University of Notre Dame.

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Aging
Children, Families & Pregnancy
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Asthma,Lungs & Allergies
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Brain, Spine & Nervous System
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Diabetes, Heart and Blood Vessels
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Aging
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Browse studies by

Recently added/updated trials

Preember: A Phase 2, Open-Label Study Evaluating Imlunestrant in Premenopausal Women with Estrogen Receptor-Positive, Her2-Negative Breast Cancer

R
Rina Yadav
18 years or above
Female
Phase 2
Cohort 1: - Assess the effect of imlunestrant versus tamoxifen on tumor cell proliferation (Ki-67). - Assess the effect of imlunestrant versus imlunestrant + goserelin on tumor cell proliferation (Ki-67).Cohort 2: - Assess the rate of symptomatic or complex ovarian cysts with imlunestrant treatment without OFS.Interested in participating? For more information about this research study or other cancer-related clinical trials at IU Simon Comprehensive Cancer Center, please contact the IU Clinical Trials Office at:Email: iutrials@iu.edu Phone: (317) 278-5632

A Single Arm, Multicenter, Prospective, Open Label, Longitudinal Phase 3 Study of Prostate Specific Membrane Antigen (Psma) Positron Emission Tomography (Pet) Combined With Magnetic Resonance Imaging (Mri) Compared to Standard of Care (Soc) for the Detection of Prostate Cancer (Pca).

C
Clinton Bahler, MD
18 years - 100 years
Male
This is an open label, longitudinal Phase 3 study of prostate specific membrane antigen (PSMA) positron emission tomography (PET) combined with magnetic resonance imaging (MRI) compared to standard of care (SOC) for the detection of prostate cancer (PCa).THIS STUDY IS ENROLLING BY INVITATION ONLY - Consistent with most oncology trials, patients are not actively “recruited,” but are screened by their physician for appropriate clinical trial(s) at the time of their routine clinic visit. Occasionally, a patient may be a self-referral or physician referral, but are still screened for appropriate clinical trials at the time of their routine clinic visit. PI and staff may send copies of relevant consent forms to these patients to look over prior to actually consenting or enrolling them. This may take place at the patient's visit at which the consent is presented or the patient's next visit to the outpatient hematology/oncology clinic.  Interested in participating? For more information about this research study or other cancer-related clinical trials at IU Simon Comprehensive Cancer Center, please contact:IU Clinical Trials Office:Email: iutrials@iu.edu Phone: (317) 278-5632

A Randomized, Double-Blind, Active-Control, Multicenter Phase 3 Trial of Casdatifan and Cabozantinib Versus Placebo and Cabozantinib in Patients With Advanced Clear Cell Renal Cell Carcinoma

J
Jennifer King
18 years - 100 years
All genders
Phase 3
The purpose of the study is to evaluate the progression-free survival (PFS) of casdatifan versus placebo when each is given in combination with cabozantinib in adult patients with confirmed advanced or metastatic clear cell Renal Cell Carcinoma who have experienced progression on or after prior anti-PD-1 or anti-PD-L1 immunotherapy.Interested in participating? For more information about this research study or other cancer-related clinical trials at IU Simon Comprehensive Cancer Center, please contact:IU Clinical Trials Office Email: iutrials@iu.edu Phone: (317) 278-5632

PATIENTS PERSPECTIVES ON TREATMENT DECISION-MAKING AND THE ACCEPTABILITY AND USABILITY OF THE INTERACTIVE WEB-ENABLED COMMUNICATION RESOURCES OF THE CLL/SLL CARE ROAD MAP

L
Larry Cripe, MD
18 years - 100 years
All genders
The purpose of the study is to understand how people think about choosing between two or more treatment options and then to seek their reactions to the CLL Mind Map and Patient First Resources. Interested in participating? For more information about this research study or other cancer-related clinical trials at Indiana University Simon Comprehensive Cancer Center (IUSCCC), please contact theIU Clinical Trials Office at :Email: iutrials@iu.edu Phone: (317) 278-5632
 How Do You Move? Participants Needed for MRI Study

How Do You Move? Participants Needed for MRI Study

Alexandra Moussa-Tooks
18 years - 55 years
All genders
Why is this study being done?The purpose of this study is to understand how movement and sensory characteristics (e.g., posture, walking, hand and arm based reaching) present in psychotic disorders over time.   Who can take part?We are looking for individuals, ages 18-55, who have been diagnosed with Schizophrenia, Schizoaffective Disorder, Schizophreniform Disorder, or any other type of psychotic disorder.
 Healthy Adults Needed for MRI Study of Movement and Brain Function

Healthy Adults Needed for MRI Study of Movement and Brain Function

Alexandra Moussa-Tooks
18 years - 55 years
Accepts healthy volunteer
All genders
Why is this study being done?The purpose of this study is to understand how movement and sensory characteristics (e.g., posture, walking, hand and arm based reaching) present in psychotic disorders over time. Who can take part?We are looking for healthy individuals, ages 18-55, who have never been diagnosed with psychosis.

A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study of Ly4064809 Combined with a Cdk4/6 Inhibitor and Endocrine Therapy in Adults with Hr+, Her2- Advanced Breast Cancer with a Pik3Ca Mutation Who Received No Prior Treatment for Advanced Breast Cancer (Pikalo-2)

T
Tarah Ballinger, MD
18 years - 100 years
All genders
Phase 3
The purpose of the study is to assess the efficacy and safety of the addition of LY4064809 to other anti-cancer drugs as first treatment for advanced hormone receptor-positive (HR+)/human epidermal growth factor receptor 2-negative (HER2-) breast cancer. Participants can remain in the study as long as the drug is helping the cancer without unbearable side effects. Participants must have breast cancer that has a mutation in the PIK3CA gene. Participants must have breast cancer that has spread to other parts of the body and that expresses hormone receptors but not HER2 receptors. Interested in participating? For more information about this research study or other cancer-related clinical trials at IU Simon Comprehensive Cancer Center, please contact:IU Clinical Trials Office Email: iutrials@iu.edu Phone: (317) 278-5632