A Phase 1/Phase 2 Trial to Evaluate Safety, Immunogenicity and PSA Response of VTP-850 Prostate Cancer Immunotherapeutic in Men with Biochemical Recurrence after Definitive Local Therapy for Prostate Cancer

The University of Virginia Comprehensive Cancer Center) seeks men ages 18 and over with prostate cancer for a research study. The study will evaluate the investigational trial product called VTP-850, which is an experimental drug not yet approved by the FDA, for the treatment of prostate cancer. The main purpose of this trial is to find out how safe the trial drug VTP-850 is in people with prostate cancer who have had initial treatment but their prostate-specific antigen (PSA) levels have started to rise again.

A Single-arm, Multicenter Study to Assess the Efficacy, Safety, and Tolerability of Ropeginterferon alfa-2b-njft (P1101) in Adult Patients with Essential Thrombocythemia

The University of Virginia is conducting a clinical research study for adults ages 18 and over who have essential thrombocythemia and need to start with therapy to reduce their blood count or whose current therapy is not sufficiently controlling their disease. The purpose of the study is to learn if the study drug, P1101 (Ropeginterferon alfa-2b-njft) can normalize blood counts. The safety of P1101 will also be studied. P1101 is an FDA approved dug, but it has not been FDA approved to treat essential thrombocythemia.

A Phase 1a, Dose Escalation, Safety and Tolerability Study of NX-1607, a Casitas B-lineage lymphoma proto-oncogene (CBL-B) inhibitor, in Adults with Advanced Malignancies, with Phase 1b Expansion in Select Tumor Types

The University of Virginia is participating a clinical research study for adults ages 18 and over, who have advanced cancer. The main purpose of this study is to evaluate whether NX-1607, an oral study drug, is safe and tolerated, and to identify the highest dose that can safely be given. Another main purpose of this study is to evaluate whether NX-1607 has an effect on the cancers being studied.

DuRvalumab (MEDI4736) with chEmotherapy as first line treAtment in advanced pleural Mesothelioma - A phase 3 Randomised trial

The University of Virginia is participating a clinical research study for adults ages 18 and over, who have mesothelioma. The purpose of the study is to compare the effects of chemotherapy combined with durvalumab, a type of immunotherapy, or to a treatment chosen by your study doctor, which is either chemotherapy or immunotherapy combination (ipilimumab and nivolumab) in mesothelioma.

A Phase II Study of Ribociclib And Endocrine Treatment of Physician’s Choice for Locoregional Recurrent, Resected Hormone Receptor Positive HER2 Negative Breast Cancer (RaPhLRR Study)

The University of Virginia is conducting a clinical research study for adults ages 18 and over, who have recurrent breast cancer. The main reason for you to take part in this study is to find out if researchers can lower the chance of your breast cancer coming back again by adding a drug called ribociclib to the usual hormone therapy drugs.

A Phase 2, Randomized, Open-label Study of Onvansertib in Combination with FOLFIRI and Bevacizumab Versus FOLFIRI and Bevacizumab for Second-line Treatment of Metastatic Colorectal Cancer in Patients with a KRAS or NRAS Mutation

The University of Virginia Comprehensive Cancer Center seeks adults ages 18 and over with Metastatic Colorectal Cancer with a KRAS or NRAS Mutation to participate in a research study. The study will evaluate if the addition of the investigational agent onvansertib to standard anti-cancer treatment of FOLFIRI and bevacizumab will improve results in treating your type of cancer. Onvansertib is considered an investigational drug for use in this study because it has not been approved by the FDA.

A Phase IIIb, Single-Arm, Multicenter Study to Assess Efficacy, Safety, and Tolerability of Ropeginterferon alfa-2b-njft (P1101) in Adult Patients with Polycythemia Vera (PV)

The University of Virginia is conducting a clinical research study for adults ages 18 and over, who have Polycythemia (PV). Ropeginterferon alfa-2b-njft is an investigational drug that has been approved by the US FDA to treat PV, and the goal of Ropeginterferon alfa-2b-njft is to normalize blood counts, reduce the risk of blood clotting and bleeding, and to slow disease progression. The approved dosing for Ropeginterferon alfa-2b-njft requires a starting dose of 100 mcg and will increase 50mcg every 2 weeks.

A Phase 1, Open-Label, Study of Voruciclib in Subjects with Relapsed and/or Refractory B-Cell Malignancies or Acute Myeloid Leukemia After Failure of Prior Standard Therapies and Voruciclib in Combination with Venetoclax in Subjects with Relapsed and/or Refractory Acute Myeloid Leukemia

The University of Virginia is conducting a clinical research study for adults ages 18 and over who have relapsed and/or refractory acute myeloid leukemia. The purpose of the study is to look at the safety and efficacy of the study drug, voruciclib, alone, or in combination with venetoclax, how your body tolerates the drug or drug combination, how effective the drug(s) may be, and how the drug is taken up by your body after multiple doses over the course of the study.

Type 2 Diabetes and Dexcom G6 Continuous Glucose Monitor Research Study

The University of Virginia Center for Diabetes Technology seeks adults between the ages of 18-80 who have diagnosed with type 2 diabetes for at least one year to participate in a research study. The purpose of this study is to gather data that will be used to develop a future web-based application that will help doctors take better care of people living with type 2 diabetes. This study will ask for the collection of data that is generated as a part of your normal health care. A study Dexcom G6 Continuous Glucose Monitor (CGM) will be provided to you to use during the study.

A phase 1b/2, master protocol evaluating the safety, tolerability, pharmacokinetics, and efficacy of sotorasib (AMG 510) in subjects with advanced solid tumors with KRAS p.G12C Mutation (CodeBreaK 101)

The University of Virginia Cancer Center is conducting a clinical research study for patients who are adults ages 18 and over, and have a KRAS pG12C mutation in lung or colorectal cancer. The purpose of this study to evaluate an investigational drug, sotorasib in combination with chemotherapies or another investigational drug. The safety and effects of the investigational treatment will be assessed for this study.