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Barnes Jewish Hospital

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Saint Louis, Missouri 63110

Global Leader in Lung Cancer

Global Leader in Breast Cancer

Conducts research for Lymphoma

Conducts research for Heart Failure

Conducts research for Leukemia

384 reported clinical trials

35 medical researchers

Photo of Barnes Jewish Hospital in Saint LouisPhoto of Barnes Jewish Hospital in Saint LouisPhoto of Barnes Jewish Hospital in Saint Louis

Summary

Barnes Jewish Hospital is a medical facility located in Saint Louis, Missouri. This center is recognized for care of Lung Cancer, Breast Cancer, Lymphoma, Heart Failure, Leukemia and other specialties. Barnes Jewish Hospital is involved with conducting 384 clinical trials across 607 conditions. There are 35 research doctors associated with this hospital, such as Yan Wang, David G Mutch, M.D., Ramzi Abboud, M.D., and Puja Kachroo, MD.

Area of expertise

1

Lung Cancer

Global Leader

Barnes Jewish Hospital has run 33 trials for Lung Cancer. Some of their research focus areas include:

Stage IV
PD-L1 positive
Stage III
2

Breast Cancer

Global Leader

Barnes Jewish Hospital has run 20 trials for Breast Cancer. Some of their research focus areas include:

Stage IV
HER2 positive
Stage III

Top PIs

Clinical Trials running at Barnes Jewish Hospital

Breast Cancer

Stroke

Multiple Myeloma

Atrial Fibrillation

Relapse

Atrial Flutter

Cardiovascular Disease

Heart Disease

Aortic Stenosis

Aortic Aneurysm

Image of trial facility.

PF-07220060 + Letrozole

for Breast Cancer

The purpose of this study is to determine the safety and efficacy of PF-07220060 with letrozole compared to approved treatments (ie, palbociclib, ribociclib or abemaciclib with letrozole) in people with breast cancer: * HR-positive (breast cancer cells that need estrogen or progesterone to grow) * HER2-negative (cells that have a small amount or none of a protein called HER2 on their surface); * locally advanced (that has spread from where it started to nearby tissue or lymph nodes) or metastatic disease (the spread of cancer to other places in the body) * who have not received any prior systemic anti-cancer treatment for advanced/metastatic disease. Approximately half of the participants will receive PF-07220060 plus letrozole while the other half of participants will receive the investigator's choice of treatment plus letrozole. The study team will monitor how each participant is doing with the study treatment during regular visits at the study clinic.

Recruiting

2 awards

Phase 3

4 criteria

Image of trial facility.

PF-07248144 + Fulvestrant

for Breast Cancer

The purpose of this study is to learn about the safety and effects of the study medicine PF-07248144 when given along with fulvestrant for the possible treatment of HR-positive, HER2-negative advanced or metastatic breast cancer. HR-positive breast cancer cells have proteins on their surface called receptors that bind to hormones like estrogen and progesterone (female sex hormones). These hormones can promote the growth of cancer cells. HER2-negative describes cells that have a small amount or none of a protein called HER2 on their surface. In normal cells, HER2 helps control cell growth. Cancer cells that are HER2-negative may grow more slowly and are less likely to recur (come back) or spread to other parts of the body than cancer cells that have a large amount of HER2 on their surface. Advanced cancer is a term that is often used to describe cancer that is unlikely to be cured. Metastatic cancer is the type where the cancer cells spread from one part of the body to another. This study is seeking for participants whose breast cancer has gotten worsen after receiving cyclin dependent kinase (CDK) 4/6 inhibitor-based therapy. Half of participants in this study will receive their usual study treatment, everolimus with endocrine therapy (either exemestane or fulvestrant) for HR-positive/HER2-negative advanced or metastatic breast cancer (A/mBC). The study doctor will discuss which hormone therapy is right for the participant before treatment begins. PF-07248144 is a tablet that will be taken by mouth at home every day in a 28-day cycle. Fulvestrant will be given as two injections (one injection in the buttock) at visits to the study clinic. Everolimus and exemestane are also tablets and will be taken by mouth at home every day in a 28-day cycle. The study will compare the experiences of people receiving PF-07248144 in combination with fulvestrant to those of the people who do not. This will help see if PF-07248144 in combination with fulvestrant is safe and effective.

Recruiting

2 awards

Phase 3

4 criteria

Image of trial facility.

Disitamab Vedotin + Tucatinib

for Breast Cancer

This clinical trial is studying solid tumor cancers. A solid tumor is one that starts in part of your body like your lungs or liver instead of your blood. Once they've grown bigger in one spot or spread to other parts of the body, they're harder to treat. This is called advanced or metastatic cancer. Participants in this study must have breast cancer or gastric cancer. Participants must have tumors that have HER2 on them. This allows the cancer to grow more quickly or spread faster. There are few treatment options for patients with advanced or metastatic solid tumors that express HER2. This clinical trial uses an experimental drug called disitamab vedotin (DV). Disitamab vedotin is a type of antibody drug conjugate or ADC. ADCs are designed to stick to cancer cells and kill them. This clinical trial uses a drug called tucatinib, which has been approved to treat cancer in the United States and some other countries. This drug is sold under the brand name TUKYSA®. This study will test how safe and how well DV with tucatinib works for participants with solid tumors. This study will also test what side effects happen when participants take these drugs. A side effect is anything a drug does to the body besides treating the disease.

Recruiting

1 award

Phase 2

6 criteria

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