This is a listing of Loyola University Health System clinical research that is open and actively recruiting patients. Please click on the name of the research for a brief description, eligibility requirements and contact information. All research listed below have been approved by Loyola's Institutional Review Board chairman for promotion on our Web site.
For more information call (888) LUHS-888.
Treatment of Individuals Needing a Foot and Ankle Fusion Using an Investigational Device Compared to Using the Individual’s Own Bone Graft During the SurgeryThis study is being done to determine if the investigational device used during the standard fusion procedure is safe and effective as a bone regeneration system when used during bone fusion surgery in individuals with foot and ankle problems when compared to using the individual’s own bone (autologous bone graft is when bone is taken from another site in an individual’s body).
A Study to Compare Radiotherapy Alone Versus Radiotherapy with Concurrent Chemotherapy (with the drug temozolomide) Versus Radiotherapy with Adjuvant Chemotherapy Versus Radiotherapy with Concurrent and Adjuvant Chemotherapy.The purpose of this study is to determine whether the addition of temozolomide treatment to radiotherapy (concomitant treatment) or the addition of temozolomide treatment after completion of radiotherapy on five days out of every 28 days for 12 months (adjuvant treatment) will improve the results of the treatment. This study will find out what effects, good and/or bad, the addition of temozolomide has when it is given at the same time as radiotherapy, after radiotherapy or both.
Evaluation of Unlicensed Cord Blood Units in Pediatric and Adult PatientsTo provide access to cord blood for those recipients whose best choice for cord blood does not meet all FDA standards but does meet study standards set by the National Marrow Donor Program. This study will assess how well and how quickly recipients’ blood counts return to normal after transplant.
Ezatiostat hydrochloride in individuals with lenalidomide refractory or resistant myelodysplastic syndrome (MDS)The overall purpose of this study is to find out what the effects, good and/or bad, ezatiostat hydrochloride treatment has on you and your type of MDS.
Steroids plus ALD518 vs. Steroids Alone after Allogeneic Stem Cell Transplant for Participants with Acute GVHD (Graft vs. Host Disease).The purpose of this trial is to test the good and bad effects of ALD518 at differing dose levels in two groups of participants with acute graft vs. host disease.
Treatment Therapy Followed by Umbilical Cord Stem Cell TransplantThe primary objective of this study is to measure progression free survival in the elderly at three years after umbilical cord stem cell transplantation, which may include an expanded umbilical cord stem cell unit and using pre-transplant conditioning of fludarabine, cyclophosphamide and total body irradiation.
Vaccine Study for the Prevention of Shingles in Individuals with CancerThe purpose of this study is to test the safety, tolerability and effectiveness of the vaccine, V212, on participants with cancer.
A Comparison of Comparing the Effects, Good and/or Bad, of a Standard Lymph Node Removal Versus an Extended Lymph Node Removal for Participants with Bladder Cancer.The purpose of this study is to compare the effects, good and/or bad, of performing a standard lymph node removal versus an extended lymph node removal.
A Study Comparing the Combination of Gemcitabine, Cisplatin and Bevacizumab on Transitional Cell Carcinoma of the Urinary TractThe purpose of this study is to see what effects, good and/or bad, the combination of gemcitabine, cisplatin and bevacizumab has on participants and their cancer.
Bone Health in the Jaw of Cancer PatientsThe purpose of this study is to learn how often ONJ occurs in participants who cancer has spread to the bone and are being treated with zoledronic acid during a three-year time period after starting treatment. This study will also identify risk factors associated with ONJ.
A Comparison Study of Two Radiation Therapies for Early-Stage Breast Cancer: A Brief Treatment Period at Higher Dose vs. Standard Dose over Longer Treatment Period.The purpose of this study is to compare two approaches to radiation therapy: One therapy would entail a higher daily dose during the course of three weeks with a boost given on each day of radiation therapy. The other therapy would entail standard whole breast radiation followed by a boost given on separate days extending over the course of six to seven weeks.
A Comparison of Two Different Treatments for Participants with HER2- positive Breast Cancer.This trial will compare which of two treatments is most effective for participants with HER2- breast cancer.
A randomized phase III study of whole breast radiation versus partial breast radiation for women with breast cancerThe purpose of this study is to see if partial breast irradiation is as good as or better than whole breast irradiation in keeping cancer from coming back in the breast.
Breast Radiation Using Mammosite Brachytherapy (after breast conserving surgery)The purpose is to test whether radiation to part of the breast using brachytherapy after the removal of cancer gives similar results to those obtained when the whole breast receives radiation therapy. The study seeks to assess safety of the mammosite device in this setting, including the quality of life.
Comparing Different Chemotherapy Regimens to Treat Breast Cancer Before Having SurgeryThe purpose of this study is to compare different chemotherapy treatments and determine which is better for breast cancer patients.
Comparing Standard Endocrine Therapy and Chemotherapy in Women with Hormone-responsive Breast CancerThe purpose of this study is to find out if the recurrence score can help decide whether participants should receive chemotherapy or not.
Comparing the Effects of Trastuzumab Emtansine With Currently Available Treatments for HER2-Positive Locally Advanced or Metastatic Breast CancerThe purpose of this study is to compare the effects, good and/or bad, of trastuzumab emtansine (previously known as T-DM1) with currently available treatments on you and your breast cancer to find out which therapy is better. In this study, you will receive either trastuzumab emtansine or the treatment regimen of your study physician’s choice (TPC).
Comparison of Metformin and Placebo on Recurrence and Survival in Breast CancerThe purpose of this study is to find out whether it is better to receive the drug Metformin with the usual treatment for breast cancer or not.
Comparison of Standard Chemotherapy and Standard Chemotherapy with Investigational DrugsThe purpose of this study is to determine how women with breast cancer will respond to standard chemotherapy versus standard chemotherapy with investigational drugs.
Comparison of Surgery Plus Radiation Versus the Standard Approach of Continued Treatment with Medication in Individuals with Metastatic Breast CancerThe purpose of this study is to compare the good and/or bad effects of a new approach that includes surgery plus radiation for the tumor in your breast to the standard approach of continued treatment with medication.
Pathological Studies on Breast Cancer TissueThe purpose of the study is to analyze tumor specimens from breast cancer participants.
Recurrent Breast Cancer StudyThe purpose of this study is to determine how effective combining carboplatin, ABI-007 and bevacizumab are in the advanced breast cancer.
Study Comparing Radiation Therapy With or Without Trastuzumab in Women With Early Stage Breast CancerThis purpose of this study is to find out if adding trastuzumab to breast radiation therapy is more effective than radiation therapy without trastuzumab in preventing occurrence of breast cancer in the same breast, in the other breast or in other parts of the body in patients with early stage breast cancer.
Study Using Two Investigational Drugs for Individuals with Breast Cancer who have Progressed while Receiving Prior TherapyThe purpose of this study is to determine how safe and tolerable this combination of the two investigational drugs is in certain individuals with breast cancer. This extension study is designed to allow individuals who are benefitting from the combination to continue their treatment.
Study to Evaluate Fatigue in Participants in the NCIC CTG MA.32 TrialTo evaluate fatigue in participants in the NCIC CTG MA.32 trial.
The Effectiveness of AUY922 in Combination with Trastuzumab in Individuals with Locally Advanced or Metastatic HER2-positive Breast CancerThe purpose of this study is to find out the effectiveness of the investigational drug AUY922 when given in combination with trastuzumab.
The Effects of Trastuzumab on Standard Treatment with Chemotherapy for Early Stage, HER2-low Breast CancerThe main purpose of this study is to learn if adding a targeted therapy, trastuzumab, to standard treatment with chemotherapy for early stage, HER2-low breast cancer, will prevent breast cancer from returning.
Study Comparing Standard Radiation Therapy Treatment to an Investigational Treatment of Radiation Therapy Combined with Chemotherapy in Patients with Cervical CancerThe purpose of this study is to determine if the investigational treatment is better than the standard treatment.
Comparing Certain Chemotherapy Treatments for Cervical CancerThe purpose of this study is to determine which chemotherapy treatment results in improved overall survival.
Chemotherapy in Individuals with Advanced Colon CancerThis study is being conducted to evaluate the effects (good and bad) of different chemotherapy treatments. One of the common combinations of chemotherapy drugs used to treat colon cancer includes 5-fluorouracil (also called 5-FU), leucovorin and oxaliplatin, and is called “FOLFOX.” At the present time, the Food and Drug Administration (FDA) has approved each of these drugs as treatment for colon cancer. FOLFOX is a standard treatment used to prevent colon cancer from coming back (recurrence).
The Study of mFOLFOX7 or XELOX Plus Bevacizumab Versus 5-Fluorouracil/Leucovorin or Capecitabine Plus Bevacizumab in Individuals 70 Years of Age or Older with Colorectal CancerThe purpose of this research study is to compare the length of time during and after treatment that metastatic colorectal cancer does not get worse in older patients treated with bevacizumab plus either 5-fluorouracil/leucovorin or capecitabine without oxaliplatin, or in patients treated with bevacizumab plus 5-fluorouracil/leucovorin or capecitabine with oxaliplatin. All of the study drugs have been FDA-approved for the treatment of metastatic colorectal cancer.
The study of medications in participants with previously untreated colorectal cancer.The purpose of this study is to learn if certain levels of biomarkers (for example, ERCC-1 as a marker for chemotherapy resistance and VEGF-A as a marker for a response to bevacizumab) can be used to determine how well colorectal cancer will respond to bevacizumab plus mFOLFOX6 or FOLFIRI by changes in how genes and proteins are regulated in response to bevacizumab or chemotherapy. A biomarker is measured and evaluated using blood and/or tissue.
A Study Comparing the Effectiveness and Side Effects of Paclitaxel Given Every Three Weeks Versus Paclitaxel Given Once a Week, When Combined with Carboplatin for Patients with Epithelial Ovarian, Peritoneal or Fallopian Tube CancerThe purpose of this study is to compare the effectiveness and side effects of paclitaxel given every three weeks versus paclitaxel given once a week, when combined with carboplatin.
A Study to Evaluate the Addition of the Study Drug Cetuximab to the Standard Therapy Regimen for Esophageal Cancer Patients Who Are Treated Without Surgery.The purpose of this study is to see if adding the study drug cetuximab to the standard treatment drugs paclitaxel and cisplatin, along with radiation therapy, will improve overall survival for individuals with esophageal cancer who are unable to have surgery, or choose not to have surgery.
The Study of Adding the Drug Trastuzumab to the Standard Chemotherapy and Radiation Therapy Plan for Individuals with Esophageal CancerThe purpose of this study is to determine whether the addition of the drug trastuzumab to the standard treatment regimen for esophageal cancer can help prevent your cancer from growing back.
Chemotherapy and Radiation for Participants With Cancer in the Bile Duct or GallbladderThe purpose of this study is to find out what effects, good and/or bad, capecitabine, gemcitabine and radiation have on you and your cancer of the bile duct or gallbladder.
The Study of MK-2206 in Individuals with Gastric or Gastroesophageal Junction (GEJ) Cancer that has Worsened or Returned after TreatmentThe purpose of this study is to find out what effects, good and/or bad, MK-2206 has on you and your gastric or gastroesophageal junction (GEJ) cancer. MK-2206 is an investigational drug that has not been approved by the FDA for use in this type of cancer.
A Study of Radiation Therapy Plus or Minus the Drug Cetuximab in the Treatment of Head and Neck Cancer.The purpose of this study is to compare the effects, good and/or bad, of radiation therapy alone with radiation therapy and cetuximab on you and your cancer. In this study, you will receive either radiation therapy alone or radiation therapy and cetuximab.
Chemotherapy in Patients With Recurrent Head and Neck CancerThe purpose of this study is to compare the effects (good and bad) of the addition of bevacizumab to standard chemotherapy (cisplatin and docetaxel or cisplatin and 5-FU) and to determine if the combination of standard chemotherapy and bevacizumab can increase the effectiveness of treatment for head and neck cancer. This combination is experimental.
The study of radiation therapy plus the drug cetuximab versus radiation therapy plus the drug cisplatin for the treatment of HPV-associated oropharynx cancer.The purpose of this study is to compare the effects, good and/or bad, of two standard treatments for head and neck cancer: radiation therapy and cisplatin or radiation therapy and cetuximab. The two treatments may be comparable in treating your cancer, but radiation and cetuximab may result in less severe side effects.
A Comparison of Everolimus Alone Versus the Combination of Everolimus and Bevacizumab for Advanced Kidney CancerThe purpose of this study is to compare the effects of a drug called everolimus alone with those of the combination of everolimus and a drug called bevacizumab for advanced kidney cancer to find out which is better. In this study, you will get either the combination of everolimus and a placebo or the combination of everolimus and bevacizumab.
Chemotherapy in Patients Who Have Cancer of the Kidney That Has Spread to Other Organs of the BodyThe purpose of this study is to compare the safety and effectiveness of the study drug Everolimus given before sunitinib versus sunitinib given before the study drug Everolimus, to determine the most effective order to give sunitinib and Everolimus to slow tumor growth and to determine which study treatment schedule has less side-effects.
The Study of a Commercial Medication in Individuals with Kidney CancerThe purpose of this study is to see whether treatment with everolimus after surgery for kidney cancer will increase the time without cancer returning.
A Randomized Study Comparing the Placebo or Study Drug Plus the Standard Medication that is Used to Prevent Moderate to Severe Chronic Graft Vs. Host Disease in Adult Participants with Acute Myeloid Leukemia, Acute Lymphoid Leukemia or Myelodysplastic Syndrome after Allogeneic Stem Cell Transplantation from Unrelated Donors.The primary reason for this study is to test the effect of the study drug or placebo when combined with the standard preventive drugs for Graft Vs. Host Disease (GVHD).
A Study Combining Epratuzumab with Cytarabine and Clofarabine for Relapsed or Refractory Acute Lymphoblastic Leukemia (ALL)The purpose of this study is to test the effects of combining clofarabine, cytarabine and epratuzumab on precursor B-cell acute lymphoblastic leukemia.
A Study Evaluating the Safety and Efficacy of Combining Two Drugs for Participants Age 60 and Older on Previously Untreated Acute Myeloid LeukemiaThe purpose of this study is to find out the safety and efficacy of combining two drugs, azacitidine and gemtuzumab ozogamicin, to treat participants age 60 or older for untreated acute myeloid leukemia.
A Study Investigating the Addition of Pravastatin to Chemotherapy for the Treatment of Relapsed Acute Myelogenous LeukemiaThe purpose of this study is to see what effects, good and/or bad, that adding pravastatin, a drug usually used to treat high cholesterol, to chemotherapy has on relapsed acute myelogenous leukemia.
A Study of the Combination of Chemotherapy and Dasatinib with or without Stem Cell Transplant on Acute Lymphoblastic LeukemiaThe purpose of this study is to find out what effects, good and/or bad, the investigational drug dasatinib has on you and your leukemia.
Leukemia Relapse TrialThe purpose of this study is to determine patient outcomes following high-dose combination chemotherapy treatment and to compare higher versus standard dose vincristine chemotherapy.
Risk-adapted Chemotherapy in Younger Patients with Newly Diagnosed Standard-risk Acute Lymphoblastic LeukemiaDrugs used in chemotherapy work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Giving more than one drug (combination chemotherapy), giving the drugs in different doses, and giving the drugs in different combinations may kill more cancer cells. Children will be placed in groups according to the results of biology testing done on the child’s bone marrow. According to these studies, the low-risk children get less intense treatment, and the higher-risk children will be treated on a high-risk study.
Treatment with Clofarabine in Newly Diagnosed Acute Myeloid Leukemia in Adults Ages 60 Years or OlderThe purpose of the study is to compare the effect of clofarabine versus standard therapy in newly diagnosed acute myeloid leukemia (AML) patients who are 60 years of age or older.
Ramp-up Sorafenib TrialThe main purpose of this study is to see if subjects can tolerate treatment better if they start taking smaller doses of sorafenib and then gradually increase their dose to two tablets twice a day.
The Study of Sorafenib and Chemotherapy in Individuals Who Have Liver Cancer (Hepatocellular Carcinoma) That is Not Removable by Surgery and the Cancer Has Not Spread Outside the LiverThe purpose of this study is to see if adding the oral chemotherapy pill, sorafenib, to localized chemotherapy (chemoembolization) to the liver will help individuals to live longer than treatment with localized chemotherapy to the liver without sorafenib.
Additional Chemotherapy Drug after surgical removal of Non Small Cell Lung CancerThe purpose of this study is to determine if adding the new drug bevacizumab to chemotherapy improves the chance for cure for patients who have had surgery for the removal of the lung cancer and to compare the effects (good and bad) of adding bevacizumab to chemotherapy compared to standard chemotherapy alone. Bevacizumab works by preventing the formation of new blood vessels, including those that surround and supply cancer cells, with the oxygen and nutrients they need to survive and grow.
Chemotherapy Agents in Patients With Lung Cancer That Has Grown Despite Earlier Treatment With ChemotherapyThe purpose of this study is to compare the effects, good and/or bad, of topotecan alone with topotecan plus AVE0005 to find out which is better. We would also like to find out more about the effects, good and/or bad, that weekly topotecan causes.
Chemotherapy in Individuals With Lung CancerThe primary objective of this study is in patients with advanced NSCLC treated with carboplatin, paclitaxel and bevacizumab (if appropriate) with or without cetuximab, to compare overall survival (OS) in the entire study population; progression-free survival (PFS) by institutional review in EGFR FISH-positive patients. The secondary objectives are in patients with advanced NSCLC treated with carboplatin, paclitaxel and bevacizumab (if appropriate) with or without cetuximab, to compare OS and PFS by centralized review in EGFR FISH-positive patients; PFS by centralized image review and by institutional review in the entire study population. To compare the response rate (confirmed plus unconfirmed, complete and partial responses) in the subset of patients with measurable disease in EGFR FISH-positive patients; the entire study population. The purpose of this study is to compare the effects, good and/or bad, of cetuximab on lung cancer.
Chemotherapy in Patients who have Advanced Lung CancerThe purpose of this study is to find out if the combination of gemcitabine plus carboplatin and BSI-201 works better than gemcitabine and carboplatin alone in patients with stage IV squamous non-small-cell lung cancer (NSCLC) that has not previously been treated. The standard chemotherapy combination contains two drugs, carboplatin and gemcitabine. In this research study, a drug called BSI-201 will be added to these two chemotherapy drugs. The combination of gemcitabine, carboplatin and BSI-201 has not been tested as a lung cancer treatment and is investigational.
Pazopanib & weekly Paclitaxel Chemotherapy in Patients With Advanced Lung CancerThe purpose of this study is to learn about the good and bad effects of pazopanib when it is given with a chemotherapy drug called paclitaxel to treat advanced lung cancer.
A Randomized Study Using RAD001 Adjuvant Therapy Versus Placebo in Patients With Diffuse Large B-cell Lymphoma Who Have Achieved Complete Reponse With First-line Rituximab-chemotherapyThe purpose of this study is to learn if the study drug RAD001 can slow or prevent the recurrence of your cancer compared to a placebo.
A Randomized Study for Untreated Mantle Cell Lymphoma Patients 65 Years Old or Under With Treatment of Either R-HCVAD/MTX/Ara-C Chemotherapy With an Autologous Stem Cell or R-Bendamustine Chemotherapy With an Autologous Stem Cell Transplant.The purpose of this study is find out what effects, good and/or bad, a combination of drugs called “R-HCVAD/MTX/ARA-C” compared to “R-bendamustine” followed by a stem cell transplant has on mantle cell lymphoma.
A Study Combining Vorinostat with Rituximab, Cyclophosphamide, Doxorubicin, Prednisone and VincristineThe purpose of this study is to determine the safety, effectiveness and maximum tolerated dose of vorinostat in combination with rituximab, cyclophosphamide, doxorubicin, prednisone and vincristine.
Chemotherapy Treatments for Diffuse Large B-cell Lymphoma.The purpose of this study is to compare the effects (good and bad) of two treatments for lymphoma. The treatments are known as R-CHOP and DA-EPOCH-R. Another goal of the study is to analyze your tumor using new scientific laboratory studies to better understand your type of lymphoma.
Medication Study for Relapsed Hodgkins LymphomaThis study is for people with relapsed or refractory Hodgkins lymphoma. The purpose is to see what effects (good and bad) a drug called temsirolimus has on you and your lymphoma.
Treatment Therapy Followed by Autologous Stem Cell TransplantThe primary objective of this study is to measure the level of busulfan chemotherapy and adjust the dose for each individual according to the level in the person’s blood during the preparative chemotherapies, followed by autologous hematopoietic stem cell transplant in people with Non-Hodgkin’s lymphoma and Hodgkin’s lymphoma.
Treatment Therapy Followed by Stem Cell Transplant for Relapsed Follicular Non-Hodgkin’s LymphomaThe primary objective of this study is to measure progression-free survival at two years after allogeneic hematopoietic stem cell transplantation (HSCT) using pre-transplant conditioning of fludarabine, cyclophosphamide and rituximab (FCR) for patients with relapsed follicular non-Hodgkin’s lymphoma.
Treatment Therapy for Hodgkin’s Lymphoma Patients With Disease Present After an Autologous Stem Cell TransplantThe primary objective of this study is to compare the progression-free survival of patients that have residual disease or disease that has not resolved using best supportive care with a placebo versus best supportive care with SGN-35.
Treatment Therapy to Mobilize and Collect Stem Cells for Autologous Stem Cell Transplant in Patients with Non-Hodgkin’s Lymphoma Weighing =154 lbThe primary objective of this study is to measure the number of stem cells collected for autologous stem cell transplant in patients with Non-Hodgkin’s lymphoma (NHL) using fixed dose of plerixafor in combination with G CSF as compared to the standard weight-based dose of plerixafor in combination with G CSF.
Treatment for Newly Diagnosed Hodgkin’s Lymphoma Based on PET Scan Results Following Two Cycles of Standard Treatment with ABVD ChemotherapyThe purpose of this study is to find out if we can determine the type of chemotherapy you may need to treat your Hodgkin’s lymphoma and whether or not you will need radiation therapy in addition to chemotherapy based on the results of your PET scan.
Treatment of Aggressive Hodgkin Lymphoma Based on PET Scan ResultsThis study will follow PET scan results to determine if your disease is responding to standard treatment for your Hodgkin lymphoma. If it is not responding, you will be switched to a more intensive treatment plan.
Treatment of Non-Hodgkins Lymphoma for Individuals Who Have Been Previously Treated or Who are Ineligible for or Have Previously Received an Autologous Stem Cell TransplantThe purpose of this study is to see if the study drug plus rituximab is safe and if it will stop your cancer from growing or cause your cancer to shrink.
Treatment of Relapsed Mantle Cell Non-Hodgkin’s Lymphoma With LenalidomideThe purpose of this study is to see what effects (good and bad) a drug called lenalidomide has on you and your lymphoma.
Clinical trial researching an investigational drug for lymphoma patientsTo evaluate the benefits of an investigational drug in patients with relapsed or refractory lymphoma
Umbilical Cord Blood Transplant Followed by Infusion at 24 Hours Post-Transplant of Blood Cells (Expanded Human Myeloid Progenitor Cells)The purpose of this study is to measure the safety of ex vivo expanded human myeloid progenitor cells. Expanded human myeloid progenitor cells have the ability to make red blood cells, platelets and some kinds of white blood cells.
A Study Combining Bendamustine with Bortezomib, Lenalidomide and Dexamethasone for the Treatment of Relapsed or Refractory Multiple MyelomaThe purpose of this study is to determine the safety, effectiveness and maximum tolerated dose of bendamustine in combination with bortezomib, lenalidomide and dexamethasone.
A Study Comparing the Combination of Bortezomib and Dexamethasone with Panobinostat or Placebo in Individuals with Multiple MyelomaThe purpose of this study is to find out whether the combination of panobinostat, bortezomib and dexamethasone is safe and results in a better anti-myeloma activity than bortezomib and dexamethasone alone.
High-dose Busulfan and Melphalan followed by Bortezomib (BuMelVel) as Chemotherapy prior to Autologous Stem Cell Transplantation for Multiple MyelomaThe purpose of this study is to evaluate the effectiveness of high-dose busulfan and melphalan followed by bortezomib as chemotherapy prior to autologous stem cell transplantation for individuals with multiple myeloma and to measure the level of cells in the blood in order to evaluate disease response.
Comparing Treatments for Ovarian Cancer That Has RelapsedThe purpose of this study is to compare different treatments for ovarian cancer that has relapsed.
Comparison of Erlotinib in Combination with Gemcitabine Versus Gemcitabine Alone in Individuals with Pancreatic Cancer that was Removed by SurgeryThe purpose of this study is to compare the effects, good and/or bad, of the study drug erlotinib in combination with gemcitabine versus gemcitabine alone for individuals with pancreatic cancer that was removed by surgery.
The Study of Dendritic Cell Vaccine in Individuals who have Pancreatic Cancer that cannot be Surgically RemovedThe purpose of this study is to determine the safety and effectiveness of this new two-part therapy. The radiation is typically given as a daily treatment Monday - Friday for four to five weeks, but in this study, it will be given as doses over a two-week period using only a high-dose strategy. Following this, a vaccine will be injected into your pancreatic tumor, under either ultrasound or CT-scan guidance as an experimental procedure, to see if we can shrink the tumor so that it can then be removed surgically. A secondary purpose of the research project is to see if the vaccine stimulates your immune system.
A Phase III Trial Comparing the Effectiveness of Three Treatment Methods for Prostate Cancer in Individuals who have a Rising PSA after having a Radical ProstatectomyThe purpose of this study is to compare the effects of three treatment methods for men with prostate cancer who have a rising PSA after prostatectomy surgery. The three methods are: radiation to the prostate bed only, hormone therapy for four to six months plus radiation therapy to the prostate bed, or hormone therapy for four to six months plus radiation therapy to the prostate bed and to the pelvic lymph nodes.
A Study Comparing Hormone Therapy with or without IMC-A12 in Individuals with New Hormone-sensitive Metastatic Prostate CancerThe purpose of this study is to find out what effects, good and/or bad, there are to adding IMC-A12 to standard hormone therapy (bicalutamide and goserelin acetate or leuprolide acetate).
A Study Comparing Radiation Therapy with or without Hormone Therapy for Individuals with Intermediate-risk Prostate Cancer.The purpose of this study is to compare the effects of radiation therapy with or without hormone therapy on individuals with intermediate-risk prostate cancer.
A Study Comparing the Effects of Abiraterone Acetate Treatment with Hormone Therapy on Participants with Prostate Cancer.The purpose of this study is to find out what effects, good and/or bad, abiraterone acetate has on you and your prostate cancer.
A Study Evaluating Early Treatment With Zoledronic Acid for Men With Prostate CancerThe purpose of this study is to determine if early treatment with zoledronic acid delays bone problems for men with prostate cancer involving the bone.
A Combination of Chemotherapy (Including Cetuximab), Radiation Therapy and Surgery for Participants With Stage II or III Rectal CancerThe purpose of this study is to find out what effects, good and/or bad, the combination of the chemotherapies, radiation therapy and surgery has on the participant and their rectal cancer.
A Study to Compare Radiation Therapy and Chemotherapy to Radiation Therapy Alone in Individuals Who Have Had Surgical Removal of a High-risk Salivary Gland Tumor.This study will compare the effects, good and/or bad, of radiation and chemotherapy with radiation alone on your salivary gland cancer to find out which is better at reducing the chance that your cancer will come back.
A Study to Determine which Participants with Melanoma Have a Better Response to a Study Medication and to Identify Markers that may Predict Response to IL-2.The purpose of this study is to determine which participants with melanoma have a better response to IL-2 and to identify markers that may predict response to IL-2 by collecting participant information ( for example cancer diagnosis and history, prior treatments for cancer, etc.), blood and tumor samples prior to treatment and tumor measurements after treatment.
Study of an Investigational Medication in Individuals with Melanoma.The purpose of this study is to compare the effects, good and/or bad, of ipilimumab with interferon alfa-2b on you and your melanoma to find out which is better.
Comparison of a Combination of Chemotherapy Drugs to the Standard Chemotherapy Treatment for Uterine CancerThe purpose of this study is to compare a different chemotherapy combination with the current standard chemotherapy treatment for uterine cancer.
Study Comparing Standard Radiation Therapy Treatment to an Investigational Treatment of Radiation Therapy Combined with Chemotherapy in Patients with Endometrial (Uterine) CancerThe purpose of this study is to determine if the study treatment is more effective than the standard treatment of uterine cancer.
CABANA TrialAtrial fibrillation is an abnormal, rapid heart rhythm coming from the upper chambers of the heart (atria). Atrial fibrillation is the most common type of heart rhythm disorder. Instead of the heart beating in a steady pattern, in atrial fibrillation the upper chambers of the heart quiver rapidly in an unsteady manner. Atrial fibrillation may be treated with drug therapy designed to either prevent the heart rate from going too fast, or with drug therapy designed to maintain normal heart beating. In some institutions, atrial fibrillation also is treated with catheters inserted into blood vessels that can be placed inside the heart to eliminate the hot spots or triggers that start atrial fibrillation (catheter ablation). It is not known whether drug therapy or catheter ablation is better.
The Catheter Ablation Versus Anti-arrhythmic Drug Therapy for Atrial Fibrillation (CABANA) study is being done to compare drug therapy and catheter ablation in patients with atrial fibrillation. This study will help decide which treatment approach is best or when one or the other therapy is preferred. The CABANA study also will compare the cost of care for the two treatment approaches and determine the effect these therapies have on quality of life.
PRICELESSAt the time of endovascular aortic aneurysm repair surgery, a pressure-sensing device will be implanted in the aneurysm. It is permanently placed in the aneurysm sac and measures the pressure in the sac during the repair. Measurement readings from the sensor are painless and made with a device containing an antenna positioned over the abdomen.
It is believed that sensor measurements may be a useful addition to other tests that are used to measure the sac size and detect leaks from endovascular grafts.
The purpose of this research is to collect and compare sensor data with data from CT scan imaging and other diagnostic methods used in patients who have had a repair of the aneurysm.
Aortic Valve Surgery in Marfan PatientsThe purpose of the trial is to collect information on how patients do after having surgery on their aortic valve and compare the results of those who had their valve replaced to those who had the valve repaired.
Growth Hormone Deficiency StudyThe purpose of the study is to compare long-term health outcomes in patients who are lacking adult growth hormones.
Heavy Metals in the EyeThe purpose of this study is to determine the amount and type of heavy metals found in the human eye.
HIV Integrase Inhibitor-naïve Study For Experienced Anti-retroviral Therapy IndividualsThe purpose of this study is to test the effectiveness of GSK1349572 (the study drug) and to see how well it works in comparison to raltegravir, an integrase inhibitor that is avaliable to treat HIV.
Hepatitis B Trial Using Tenofovir Disoproxil Fumarate and/or Peginterferon Alpha-2aThis study is being done to see if using tenofovir disoproxil fumarate plus peginterferon alpha-2a combination therapy is better than tenofovir disoproxil fumarate alone or peginterferon alpha-2a alone.
Combination Treatment for Bipolar Depressed Participants Whose Depression Has Failed to Respond SatisfactorilyThis clinical trial will investigate whether bipolar depressed individuals who have not responded satisfactorily to an antidepressant will benefit from combining antidepressant therapy with an anti-inflammatory drug.
Combination Treatment for Bipolar Depressed Patients Whose Depression Has Failed to Respond SatisfactorilyThis clinical trial will investigate whether bipolar depressed individuals who have not responded satisfactorily to an antidepressant will benefit from combining antidepressant therapy with an anti-inflammatory drug.
Endothelial Function in Depressed PatientsThe purpose of this study is to determine whether depressed individuals show signs of dysfunction in their blood vessels.
ARUBAAn arteriovenous malformation (AVM), which has not ruptured, may rupture and cause death or stroke. The purpose of this study is to determine if an intervention is better for treating the symptoms (such as headache).
Gout TrialThe purpose of this study is to see whether gout patients treated with febuxostat for an extended period (approximately five years) have a higher rate of serious heart and blood vessel complications than patients who receive allopurinol. Complications include heart attacks, strokes and angina (chest pain due to narrowing of the blood vessels of the heart), which needs to be treated immediately with heart surgery. These are called major cardiovascular events.
ESPIRIT registry study for psoriasisThe purpose of this registry is to observe the degree of long-term safety of adalimumab and how well it works to treat chronic plaque psoriasis for up to 10 years. Adalimumab is a marketed drug for psoriasis. No medication is provided for this registry. Your doctor will give you a prescription for adalimumab.
PSOLAR Registry Study for PsoriasisThe registry study will track the behavior of the disease in response to other therapies, such as adalimumab, alefacept, certolizumab pegol, efalizumab, etanercept and other biologics. The registry also will evaluate clinical outcomes, quality of life and potential risks for participants who may receive standard therapies for psoriasis.
ALIAS - Albumin in acute strokeMany stroke studies have been performed looking for an effective treatment for patients who have suffered an acute ischemic stroke. Thus far, all have failed. This study seeks to determine the effectiveness of albumin versus placebo given intravaenously for stroke patients.
IRIS: Insulin Resistance Intervention After Stroke TrialBoth stroke and heart attack are serious medical problems. The purpose of this study is to see if stroke and heart attack can be reduced in insulin resistant non-diabetic adults using an approved drug versus a placebo (inactive drug).
Study of ASKP1240 in Kidney TransplantationThe purpose of this study is to determine how ASKP1240 (study drug) works to prevent rejection of your kidney transplant (anti-rejection) when used in combination with other anti-rejection medicines that are routinely used for kidney transplantation.
The purpose of the optional genetic study is to better understand the different ways in which people will respond to ASKP1240. They may be able to determine which people will receive the most benefit from receiving ASKP1240.
Respiratory Syncytial Virus (RSV) StudyThis purpose of this study is to determine the effects (both good and bad) of ALN RSV01 for the treatment of RSV.