Clinical Trials Logo

Filter by:
NCT ID: NCT00264472 Suspended - Neoplasms Clinical Trials

A Study of 5 Fluorouracil and the Anti-Tumor Activity of ADH300004 and 5 Fluorouracil in Subjects With Incurable Solid Tumors

Start date: January 2006
Phase: Phase 1
Study type: Interventional

5 fluorouracil (5 FU), one of the most actively investigated anti-cancer drugs, is rapidly inactivated by the enzyme dihydropyrimidine dehydrogenase (DPD). ADH300004 blocks DPD. This study will test the safety and effects of oral ADH300004 14 hours prior to oral 5 FU in subjects with refractory solid tumors.

NCT ID: NCT00243984 Suspended - Clinical trials for Diabetes Mellitus, Type 2

Efficacy of Topiramate for Weight Loss in Subjects With Metabolic Syndrome

Start date: March 2005
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the efficacy of topiramate compared to placebo in the treatment of obesity in metabolic syndrome. Secondary objectives include topiramate and weight loss effects on lipid levels, HbA1C, insulin resistance, and blood pressure.

NCT ID: NCT00207480 Suspended - Bacterial Vaginosis Clinical Trials

Brief, Behavioral Intervention to Reduce Douching Among Adolescent and Young Women

Start date: October 2004
Phase: Phase 1
Study type: Interventional

This study will implement and test a brief, tailored individual-level intervention to be used in two New Orleans adolescent clinics with female patients aged 16-24 who douche.

NCT ID: NCT00194883 Suspended - Clinical trials for Chronic Renal Insufficiency

Effect of Cytokines on Growth of Children With Chronic Kidney Failure

Start date: April 1997
Phase: Phase 4
Study type: Interventional

Children with chronic kidney failure often do not grow well. This study examines the possible causes of growth failure in these children and the response to recombinant human growth hormone. The growth hormone-insulin-like growth factor axis will be studied in relation to biochemical and immunological parameters as well as body compositional changes pre- and post recombinant human growth hormone therapy.

NCT ID: NCT00194636 Suspended - Prostatitis Clinical Trials

Effectiveness of Sympathetic Plexus Block on Male Pelvic Pain (Prostatitis, Prostatodynia)

Start date: November 2003
Phase: Phase 4
Study type: Interventional

The purpose of this study is to investigate, by means of a temporary sympathetic nerve block, the involvement of the sympathetic nervous system in Chronic Pelvic Pain Syndrome (CPPS). This study may also result in a new therapeutic approach for male CPPS.

NCT ID: NCT00186927 Suspended - Parainfluenza Clinical Trials

A Study to Assess the Safety of Live Intranasal Sendai Virus Vaccine in Children and Toddlers

Start date: May 5, 2005
Phase: Phase 1
Study type: Interventional

Croup is an illness of young children that is caused by a virus. With this illness, the child has fever, cough, and hoarseness. Although the illness usually gets better in 2 to 4 days, some children may be admitted to the hospital and a few infants may require an intervention to help their breathing. This illness is most often caused by a virus called parainfluenza virus type 1, but it can be caused by other viruses. The experimental vaccine that is being investigated in this study is intended to try to prevent croup caused by parainfluenza virus type 1. Currently, there are no vaccines to prevent this virus, or medications available to treat the illness once infection has occurred. This research study is testing a new experimental live-virus vaccine that is given by placing liquid drops in the nose. The Sendai virus is very similar to the virus that causes croup, but it has never been found to cause illness in people. Previous studies in animals have shown that the vaccine provided protection against the croup virus, and did not cause illness. Many people have been exposed to the Sendai virus, but no one has been known to develop illness. Several healthy adults have been given the Sendai virus vaccine being studied, and they did not experience any serious side effects or illness.

NCT ID: NCT00103623 Suspended - Prostate Cancer Clinical Trials

The Plenaxis® Experience Study

Start date: June 2004
Phase: Phase 4
Study type: Interventional

Praecis is currently conducting a 2000 patient Experience Study; this is a Phase IV commitment postmarketing safety study in the Food and Drug Administration (FDA) indicated population of patients receiving Plenaxis®. The purpose of the study is to estimate the incidence of immediate-onset systemic allergic reactions in the indicated population receiving Plenaxis® and to determine whether the hazard rate changes over time.

NCT ID: NCT00079950 Suspended - Clinical trials for Sarcoma, Soft Tissue

Efficacy and Safety Evaluation of Pegamotecan (PEG-camptothecin) in Advanced or Metastatic Soft Tissue Sarcoma

Start date: August 2003
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety and efficacy of Pegamotecan (Peg-Camptothecin) in patients with Advanced or Metastatic Soft Tissue sarcoma.

NCT ID: NCT00077493 Suspended - Lymphoma Clinical Trials

BL22 Immunotoxin In Treating Young Patients With Relapsed or Refractory Acute Lymphoblastic Leukemia or Non-Hodgkin's Lymphoma

Start date: January 2004
Phase: Phase 1
Study type: Interventional

RATIONALE: BL22 immunotoxin can locate tumor cells and kill them without harming normal cells. BL22 immunotoxin may be effective in treating relapsed or refractory acute lymphoblastic leukemia and non-Hodgkin's lymphoma. PURPOSE: This phase I trial is studying the side effects and best dose of BL22 immunotoxin in treating young patients with relapsed or refractory acute lymphoblastic leukemia or non-Hodgkin's lymphoma.

NCT ID: NCT00073853 Suspended - Spinal Cord Injury Clinical Trials

Autologous Incubated Macrophages for Patients With Complete Spinal Cord Injuries

Start date: September 2003
Phase: Phase 2
Study type: Interventional

Autologous Incubated Macrophages (ProCord) is being developed as a therapy for acute, complete spinal cord injury (SCI). The therapy is intended to reverse the loss of motor and sensory function. Following non-CNS tissue injury, macrophages quickly arrive on the scene, where they clean up cell debris, secrete different molecules thus promoting a controlled inflammatory reaction that forms the first phase of the wound healing process. While this process occurs in most tissues, including peripheral nerves, it does not occur in the CNS, where macrophages and other immune cells are relatively rare, and their activities curtailed by a biochemical mechanism known as "immune privilege." In animal studies, it appears that incubated macrophages circumvent the immune privilege, thus supporting the regrowth of axons through the injury site and enabling the recovery of neurological function. The concept derives from the pioneering research of Prof. Michal Schwartz at the Weizmann Institute of Science.