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NCT ID: NCT00038272 Completed - HIV Infections Clinical Trials

A Study of DAPD Alone Versus DAPD Plus MMF for Treatment of HIV Infection

Start date: n/a
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety, efficacy, and side effects of beta-D-2,6-diaminopurine dioxolane (DAPD) compared to DAPD plus mycophenolate mofetil (MMF) when these drugs are added to the anti-HIV treatment regimens of people infected with HIV. Some studies have shown that DAPD and MMF can help fight HIV. However, neither DAPD nor MMF has been approved by the Food and Drug Administration for treating HIV infection. This study will help doctors decide if DAPD and MMF are good drugs for treating HIV.

NCT ID: NCT00038480 Completed - HIV Infections Clinical Trials

Safety and Effectiveness of Lopinavir/Ritonavir in HIV Infected Infants

Start date: n/a
Phase: Phase 1
Study type: Interventional

The purpose of this study is to find out if the drug lopinavir/ritonavir (LPV/RTV) is safe and well tolerated in HIV infected infants. This study will also determine the most effective dose of LPV/RTV for infants.

NCT ID: NCT00038688 Completed - HIV Infections Clinical Trials

A Study of Peer Education to Prevent HIV Transmission Among Injection Drug Users and Their HIV Risk Contacts

Start date: n/a
Phase: Phase 3
Study type: Interventional

Injection drug use is the major mode of HIV transmission in many countries. Injection drug users (IDUs) transmit HIV not only through shared drug injection equipment but also through heterosexual and homosexual transmission and mother-to-child transmission. Studies have shown that peer education programs can reduce HIV risk behavior in IDUs. However, it is not known if reduced HIV risk behavior leads to fewer HIV infections. The purpose of this study is to find out if a peer education program can reduce the number of new HIV infections by changing the behavior of IDUs and their HIV risk contacts.

NCT ID: NCT00038935 Completed - Hemophilia A Clinical Trials

Study Evaluating BDDRFVIII and ReFacto AF in Hemophilia A

Start date: n/a
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine the relative bioavailability of ReFacto AF as compared to ReFacto, when each is administered as 2-minute bolus infusions.

NCT ID: NCT00039975 Completed - Hypertension Clinical Trials

Interactions Between HIV Protease Inhibitors and Calcium Channel Blockers

Start date: n/a
Phase: Phase 1
Study type: Interventional

Diltiazem CD and amlodipine are drugs used to treat heart disease and high blood pressure. The purpose of this study is to find out if these drugs interact with the anti-HIV drugs indinavir and ritonavir. The study will also look at the safety of taking the study drugs together. Heart disease and high blood pressure are major health concerns for people with HIV. Standard treatment for these illnesses often includes calcium channel blockers (CCBs). There is a potential for significant drug interactions between CCBs and HIV protease inhibitors (PIs) that may influence the dosing, monitoring, and choosing of CCBs and PIs when used in people infected with HIV. This study will examine the drug interactions between 2 commonly used CCBs and the PI combination indinavir and ritonavir (IDV/RTV). This information should help doctors choose the appropriate treatment for high blood pressure or heart disease in people taking PIs.

NCT ID: NCT00040001 Completed - Atrial Fibrillation Clinical Trials

Safety and Efficacy Study of an A1-Adenosine Receptor Agonist to Slow Heart Rate in Atrial Fibrillation

Start date: n/a
Phase: Phase 2
Study type: Interventional

This study is designed to evaluate the safety of DTI-0009 in patients with atrial fibrillation and to find the dose of DTI-0009 that lowers heart rates in patients with atrial fibrillation with rapid ventricular response.

NCT ID: NCT00040274 Completed - HIV Infections Clinical Trials

A Study of DPC 817 in HIV-Infected Males

Start date: n/a
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate DPC 817. The safety, dosages, and how the body responds to the drug will be studied.

NCT ID: NCT00040586 Completed - Prostatic Neoplasms Clinical Trials

Phase II Trial of Monoclonal Antibody (J591) in Combination With Low-Dose Subcutaneous Interleukin-2

Start date: n/a
Phase: Phase 2
Study type: Interventional

The monoclonal antibody J591 is being investigated as therapy for patients with prostate cancer, in combination with recombinant interleukin-2 (Proleukin, Aldesleukin). The study is an open-label, non-randomized phase II study for patients with documented hormone refractory prostate cancer.

NCT ID: NCT00041665 Completed - Stomatitis Clinical Trials

Recombinant Human Keratinocyte Growth Factor to Reduce Oral Mucositis in Hematologic Malignancy Patients Undergoing Peripheral Blood Stem Cell Transplantation After Radiation and High-dose Chemotherapy

Start date: n/a
Phase: Phase 3
Study type: Interventional

Radiotherapy and high dose chemotherapy with bone marrow transplantation or peripheral blood stem cell transplantation is frequently used as treatment for patients with cancers of the bone marrow or lymph nodes such as Hodgkin's disease, non-Hodgkin's lymphoma, leukemia or multiple myeloma. A common side effect of the radiotherapy and high dose chemotherapy is mucositis (inflammation of the inside of the mouth and throat resulting in pain and difficulty swallowing). Mucositis is often very severe such that patients receive intravenous nutrition and pain medication in the hospital. In this study, an investigational recombinant human growth factor called Keratinocyte Growth Factor (rHuKGF) is being evaluated to determine its protective effect on the mucosal tissue and its ability to reduce the mouth and throat soreness.

NCT ID: NCT00041860 Completed - Cancer Clinical Trials

Modulation of Benzene Metabolism by Exposure to Environment

Start date: n/a
Phase: N/A
Study type: Interventional

The research is to evaluate benzene metabolism after exposure at levels that can be found in the environment, such as the higher end concentrations in the air inside cars and buses while being driven in heavy traffic and inside private and public parking garages. To do so breath, urine, and blood samples prior to, during and after being exposed to benzene as well as benzene levels and benzene metabolites present are measured.