Dr. Timothy D. Moore

About Timothy D. Moore

Education:

• Earned a Medical degree (MD) from the University of Pittsburgh School of Medicine.
• Completed an Internship at the University of Cincinnati School of Medicine.
• Served as Chief Resident during his Residency at Mercy Hospital in Pittsburgh.
• Undertook a Fellowship in Hematology/Oncology at The Ohio State University School of Medicine.

Experience:

• Held Senior Investigator positions at the National Cancer Institute, focusing on the Cancer Therapy Evaluation Program.
• Served as an Attending physician at NCI-Navy Medical Oncology Services, Bethesda National Naval Hospital.
• Co-Medical Director for Palliative Care at The Zangmeister Cancer Center.
• Board certified in General Internal Medicine, Hematology, Medical Oncology, and Hospice & Palliative Care Medicine.

Area of expertise

Affiliated Hospitals

The Mark H Zangmeister Center

Genesis Healthcare System Cancer Care Center

Clinical Trials Timothy D. Moore is currently running

Chemotherapy + Immunotherapy

for Esophageal and Gastric Cancer

This phase III trial compares the effect of modified fluorouracil, leucovorin calcium, oxaliplatin, and irinotecan (mFOLFIRINOX) with or without nivolumab to the effect of modified fluorouracil, leucovorin calcium, and oxaliplatin (mFOLFOX) with or without nivolumab for the treatment of patients with advanced, unresectable, or metastatic HER2 negative esophageal, gastroesophageal junction, or gastric adenocarcinoma. The usual approach for patients who are not in a study is treatment with FOLFOX with some receiving an immunotherapy drug, either nivolumab or pembrolizumab, in addition to FOLFOX chemotherapy. The usual approach is defined as care most people get for cancer in the stomach, esophagus, or gastroesophageal junction. Fluorouracil is in a class of medications called antimetabolites. It stops cells from making DNA and may kill tumor cells. Leucovorin in a class of medications called folic acid analogs. When used with fluorouracil it enhances the effects of this chemotherapy drug. Irinotecan is in a class of antineoplastic medications called topoisomerase I inhibitors. It blocks a certain enzyme needed for cell division and DNA repair, and may kill cancer cells. Oxaliplatin is in a class of medications called platinum-containing antineoplastic agents. It damages the cell's DNA and may kill cancer cells. Immunotherapy with monoclonal antibodies, such as nivolumab, may help the body's immune system attack the cancer and may interfere with the ability of tumor cells to grow and spread. Some patients on this trial will receive nivolumab, in addition to mFOLFOX or mFOLFIRINOX chemotherapy. mFOLFIRINOX with or without nivolumab may be more effective than mFOLFOX with or without nivolumab by shrinking the tumor in patients with advanced, unresectable, or metastatic HER2-negative esophageal, gastroesophageal junction, or gastric adenocarcinoma.

Recruiting

2 awards

Phase 3

2 criteria

Osimertinib + Bevacizumab

for Lung Cancer

This phase III trial compares the effect of bevacizumab and osimertinib combination vs. osimertinib alone for the treatment of non-small cell lung cancer that has spread outside of the lungs (stage IIIB-IV) and has a change (mutation) in a gene called EGFR. The EGFR protein is involved in cell signaling pathways that control cell division and survival. Sometimes, mutations in the EGFR gene cause EGFR proteins to be made in higher than normal amounts on some types of cancer cells. This causes cancer cells to divide more rapidly. Osimertinib may stop the growth of tumor cells by blocking EGFR that is needed for cell growth in this type of cancer. Bevacizumab is in a class of medications called antiangiogenic agents. It works by stopping the formation of blood vessels that bring oxygen and nutrients to tumor. This may slow the growth and spread of tumor. Giving osimertinib with bevacizumab may control cancer for longer and help patients live longer as compared to osimertinib alone.

Recruiting

2 awards

Phase 3

31 criteria

More about Timothy D. Moore

Clinical Trial Related

7 years of experience running clinical trials · Led 126 trials as a Principal Investigator · 24 Active Clinical Trials

Other Doctors you might be interested in

Frequently asked questions