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A Phase 1 Dose-Escalation and Exploratory Dose Expansion Study of KRT-232 (AMG 232) in Combination with Carfilzomib, Lenalidomide, and Dexamethasone in Relapsed and/or Refractory Myeloma

The purpose of this study is to test the safety of a study drug called KRT-232 (AMG 232) when used in combination with a standard treatment regimen for relapsed or refractory multiple myeloma. The standard treatment is with the drugs carfilzomib, lenalidomide, and dexamethasone (KRd).

Phase II Study of Cabozantinib in Combination with Nivolumab and Ipilimumab in Rare Genitourinary Tumors

The purpose of this study is to test the effectiveness of the drugs cabozantinib with nivolumab and ipilimumab in rare genitourinary (GU) cancers that have no standard treatment options.

A Randomized Phase 3 Trial of Vinorelbine, Dactinomycin, and Cyclophosphamide Plus Maintenance Chemotherapy with Vinorelbine and Oral Cyclophosphamide (VINO-CPO) vs Vincristine, Dactinomycin &Cyclophosphamide Plus VINO-CPO Maintenance in HR-RMS

Rhabdomyosarcoma (RMS) is a type of cancer that occurs in the soft tissues of the body like the muscles. This study will compare the safety and effect of adding vinorelbine to vincristine, dactinomycin, and cyclophosphamide (VAC) for the treatment of patients with high risk rhabdomyosarcoma (RMS). High risk refers to cancer that is likely to recur (come back) after treatment or spread to other parts of the body.

AAML18P1 Stopping Tyrosine Kinase Inhibitors (TKI) to Assess Treatment-Free Remission (TFR) in Pediatric Chronic Myeloid Leukemia - Chronic Phase (CML-CP)

This study is for male and female children, adolescents, and young adults under the age of 25 who have been diagnosed with Chronic Myeloid Leukemia (CML) that is in the earliest phase known as the chronic phase. Chronic phase means that the level of disease is very low and is often called molecular remission.  To keep the CML at this low level, people typically take a type of drug called a tyrosine kinase inhibitor (TKI), such as imatinib, dasatinib, and nilotinib every day.
   

Randomized Phase II Study of CHO(E)P vs CC-486-CHO(E)P vs Duvelisib-CHO(E)P in Previously Untreated CD30 Negative Peripheral T-Cell Lymphomas

The purpose of this study is to compare the usual treatment to using duvelisib or CC-486 plus the usual treatment for patients with CD30 negative peripheral T-Cell lymphoma that has not been previously treated. The addition of duvelisib or CC-486 (azacitidine) to the usual treatment may or may not increase the chance of the cancer going into remission.   

A Phase 1/2 Study of M3814 (Peposertib) in Combination with Hypofractionated Radiotherapy for the Treatment of Locally Advanced Pancreatic Adenocarcinoma

The purpose of this study is to test the safety of a drug called M3814 (peposertib) in combination with a specific type of radiation therapy (hypofractionated radiation) in patients with locally advanced pancreatic cancer. This study will test different doses of M3814 to see which dose is safer for people when combined with hypofractionated radiation.

Colon Adjuvant Chemotherapy Based on Evaluation of Residual Disease (CIRCULATE-US)

This study is for people who have stage III colon cancer that has been treated with surgery but has spread to some of the lymph nodes, or who have stage II or stage III colon cancer that has been treated with surgery and has a higher risk of returning based on positive circulating tumor DNA (ctDNA) results. ctDNA is DNA that has been released from tumor cells into the bloodstream. This DNA can be measured using a blood test.
   

A Multicenter Phase II Study of Pomalidomide Monotherapy in Kaposi Sarcoma

This study is open to men and women over the age of 18 who have Kaposi Sarcoma (KS). Kaposi Sarcoma is a cancer related to a viral infection, known as the Kaposi sarcoma-associated herpesvirus, or KSHV.

Pilot Study of DS-8201a Pharmacodynamics in Patients with HER2-expressing Advanced Solid Tumors

The purpose of this study is to evaluate the study drug, DS-8201a (also known as Enhertu or fam-trastuzumab deruxtecan-nxki) for advanced solid tumors. The study aims to see how DS-8201a affects the levels of certain proteins and immune cells in solid tumors, how well it works against cancer cells, and how safe and tolerable it is.

The United States Food and Drug Administration (FDA) has approved DS-8201a for the treatment of patients with advanced HER2-positive breast or gastric cancer.