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Results: 264
This phase III trial studies how well active surveillance, bleomycin, carboplatin, etoposide, or cisplatin work in treating pediatric and adult patients with germ cell tumors. Active surveillance may help doctors to monitor subjects with low risk germ cell tumors after their tumor is removed. Drugs used in chemotherapy, such as bleomycin, carboplatin, etoposide, and cisplatin, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading.
Primary Investigator
Jasty-Rao, Rama
Secondary Protocol No
HUM00136727
NCT Number
NCT03067181
UM Number
2017.130
Phase
III
Status
OPEN TO ACCRUAL
This phase II trial studies how well inotuzumab ozogamicin works in treating younger patients with B-lymphoblastic lymphoma or CD22 positive B acute lymphoblastic leukemia that has come back (relapsed) or does not respond to treatment (refractory). Inotuzumab ozogamicin is a monoclonal antibody, called inotuzumab, linked to a toxic agent called ozogamicin. Inotuzumab attaches to CD22 positive cancer cells in a targeted way and delivers ozogamicin to kill them.
Primary Investigator
Goldman, Joshua
Secondary Protocol No
HUM00134979
NCT Number
NCT02981628
UM Number
2017.115
Phase
II
Status
OPEN TO ACCRUAL
This phase III trial studies iobenguane I-131 or crizotinib and standard therapy in treating younger patients with newly-diagnosed high-risk neuroblastoma or ganglioneuroblastoma. Radioactive drugs, such as iobenguane I-131, may carry radiation directly to tumor cells and not harm normal cells. Crizotinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Giving iobenguane I-131 or crizotinib and standard therapy may work better compared to crizotinib and standard therapy alone in treating younger patients with neuroblastoma or ganglioneuroblastoma.
Primary Investigator
Mody, Rajen
Secondary Protocol No
HUM00146837
NCT Number
NCT03126916
UM Number
2018.117
Phase
III
Status
OPEN TO ACCRUAL
Per Health Authorities guidelines for gene therapy medicinal products that utilize integrating vectors (e.g. lentiviral vectors), long term safety and efficacy follow up of treated patients is required. The purpose of this study is to monitor all patients exposed to CAR-T therapied for 15 years following their last CAR-T (e.g. CTL019) infusion to assess the risk of delayed adverse events (AEs), monitor for replication competent lentivirus (RCL) and assess long-term efficacy, including vector persistence.
Primary Investigator
Yanik, Gregory
Secondary Protocol No
HUM00096991
NCT Number
NCT02445222
UM Number
2015.001
Phase
NA
Status
OPEN TO ACCRUAL
Per Health Authorities guidelines for gene therapy medicinal products that utilize integrating vectors (e.g. lentiviral vectors), long term safety and efficacy follow up of treated patients is required. The purpose of this study is to monitor all patients exposed to CAR-T therapied for 15 years following their last CAR-T (e.g. CTL019) infusion to assess the risk of delayed adverse events (AEs), monitor for replication competent lentivirus (RCL) and assess long-term efficacy, including vector persistence.
Primary Investigator
Magenau, John
Secondary Protocol No
HUM00101108
NCT Number
NCT02445222
UM Number
2015.063
Phase
NA
Status
OPEN TO ACCRUAL
The purpose of this study is to determine whether accelerated BEP chemotherapy is more effective than standard BEP chemotherapy in males with intermediate and poor-risk metastatic germ cell tumours.
Primary Investigator
Jasty-Rao, Rama
Secondary Protocol No
HUM00155205
NCT Number
NCT02582697
UM Number
2018.161
Phase
III
Status
OPEN TO ACCRUAL
The purpose of this study is to compare the effects on low risk breast cancer receiving usual care that includes regional radiation therapy, with receiving no regional radiation therapy. Researchers want to see if not giving this type of radiation treatment works as well at preventing breast cancer from coming back.
Primary Investigator
Pierce, Lori
Secondary Protocol No
HUM00150649
NCT Number
NCT03488693
UM Number
2018.098
Phase
III
Status
OPEN TO ACCRUAL
This phase III trial studies how well carvedilol works in preventing cardiac toxicity in patients with human epidermal growth factor receptor (HER)-2-positive breast cancer that has spread to other places in the body. A beta-blocker, such as carvedilol, is used to treat heart failure and high blood pressure, and it may prevent the heart from side effects of chemotherapy.
Primary Investigator
Cobain, Erin
Secondary Protocol No
HUM00137495
NCT Number
NCT03418961
UM Number
2017.153
Phase
III
Status
OPEN TO ACCRUAL
This partially randomized phase II/III trial studies how well, in combination with surgery, cisplatin and combination chemotherapy works in treating children and young adults with hepatoblastoma or hepatocellular carcinoma. Drugs used in chemotherapy, such as cisplatin, doxorubicin, fluorouracil, vincristine sulfate, carboplatin, etoposide, irinotecan, sorafenib, gemcitabine and oxaliplatin, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Giving combination chemotherapy may kill more tumor cells than one type of chemotherapy alone.
Primary Investigator
Sedig, Laura
Secondary Protocol No
HUM00156542
NCT Number
NCT03533582
UM Number
2018.160
Phase
II
III
Status
OPEN TO ACCRUAL
This clinical trial studies cancer survivors to identify those who are at increased risk of developing late-occurring complications after undergoing treatment for childhood cancer. A patient's genes may affect the risk of developing complications, such as congestive heart failure, avascular necrosis, stroke, and second cancer, years after undergoing cancer treatment. Genetic studies may help doctors identify survivors of childhood cancer who are more likely to develop late complications.
Primary Investigator
Jasty-Rao, Rama
Secondary Protocol No
HUM00040931
NCT Number
NCT00082745
UM Number
COG ALTE03N1
Phase
NA
Status
OPEN TO ACCRUAL