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An Open Label, Phase 1, Treatment Study to Evaluate the Safety, Pharmacokinetics and Pharmacodynamics of IDE397 (MAT2A Inhibitor) In Adult Participants with Advanced Solid Tumors

The purpose of this clinical research study to find out if the experimental drug, IDE397, is safe and helpful in those who have any type of cancer that is considered a “solid tumor” (not a blood cancer) that is caused by an error in the tumor DNA associated with the gene, methylthioadenosine phosphorylase (MTAP). The loss of the MTAP gene is an error seen in many different types of cancers. Participants must have loss of the MTAP gene in order to participate in the study.
   

Dr. Mario Gaudino Awarded Grant for STICH3C Study

A seven-year grant from the Canadian Institutes of Health Research will allow investigators from Weill Cornell Medicine and Sunnybrook Research Institute to compare the outcomes of percutaneous coronary intervention (PCI) and coronary artery bypass grafting (CABG) in patients with low ejection fraction (EF). Known as STICH3C, this 750-patient study will be performed at 45 sites internationally through the Randomization of Single vs Multiple Arterial Grafts (ROMA) Trial network.

Randomized Trial of Five or Two MRI-Guided Adaptive Radiotherapy Treatments for Prostate Cancer

This is a randomized study comparing 5 radiation therapy treatments to 2 radiation therapy treatments with MRI guidance in patients with prostate cancer. The study will assess the potential benefit of limiting radiation doses received by normal tissues, namely the bladder and the rectum, with advanced MRI image guidance and to compare urinary and bowel side effects between the two treatment options.  Prostate cancer cure and control and quality of life will also be examined. 

Learn more about the trial details in this informational video:

A Phase 2 Trial of Paxalisib Combined with a Ketogenic Diet and Metformin for Newly Diagnosed and Recurrent Glioblastoma

This is a trial for adults who have a diagnosis of a malignant (cancerous) brain tumor and have either been newly diagnosed with glioblastoma and completed standard chemotherapy and radiation or have a recurrence of glioblastoma (the tumor has come back).   

A Phase 1/2 Open-Label, Multicenter Study of INCB000928 Administered as a Monotherapy or in Combination with Ruxolitinib in Participants with Anemia Due to Myeloproliferative Disorders

The purpose of this study is to evaluate the safety of an investigational drug, “INCB000928” alone and in combination with ruxolitinib (Jakafi), and to find out what effects, if any, the drug or investigational combination has on people with anemia due to myeloproliferative disorders.

This is an open-label study, which means that both you and your study doctor will know whether you are receiving study drug alone or the investigational combination.

A Randomized Phase 3 Trial of Nivolumab in Combination with Chemo-immunotherapy for the Treatment of Newly Diagnosed Primary Mediastinal B-cell Lymphoma

Treatment for Primary Mediastinal (Thymic) Large B-Cell Lymphoma (PMBCL) involves chemotherapy combined with an immunotherapy called rituximab. This combination is also known as the chemo-immunotherapy backbone. There are two types of chemo-immunotherapy backbone treatments for PMBCL: either R-CHOP or DA-EPOCH-R.
   
These drugs effectively treat PMBCL, but are known to cause long-term side effects at high doses. Side effects are unintended and unwanted results of treatment. Study doctors are interested in finding an effective treatment that improves the outcome of PMBCL.
   

A Phase 3 Randomized Trial for Patients with de novo AML Comparing Standard Therapy Including Gemtuzumab Ozogamicin (GO) to CPX-351 with GO, and the Addition of the FLT3 Inhibitor Gilteritinib for Patients with FLT3 Mutations

Treatment for acute myeloid leukemia (AML) involves high doses of a common class of chemotherapy drugs called anthracyclines. One anthracycline drug which is effective in treating AML is daunorubicin, but high doses are known to cause long-term side effects, especially to the heart. (Side effects are unintended and unwanted results of treatment.) Study doctors are interested in finding an effective treatment for AML patients that reduces the potential for long-term side effects.
   

The Effect of Semaglutide in Subjects with Non-Cirrhotic Non-Alcoholic Steatohepatitis

This is a study evaluating the safety and efficacy of the study drug Semaglutide in subjects with non-alcoholic steatohepatitis (NASH). An investigational/experimental drug is one that is currently being tested and has not been approved by the Food and Drug Administration (FDA) for sale in the United States. Experimental drugs such as Semaglutide may be tested in research studies such as this one.