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NCT ID: NCT00111410 Completed - Clinical trials for Rheumatoid Arthritis

Evaluating the Effect of Anakinra (r-metHuIL-1ra) on Vaccine AntibodyResponse in Subjects With Rheumatoid Arthritis (RA)

Start date: n/a
Phase: Phase 4
Study type: Interventional

The purpose of this study is to estimate the effect of anakinra, 100 mg once daily (QD), on the development of an anti-tetanus antibody response in subjects with RA after vaccination with a tetanus and diphtheria toxoids injection. In addition, this study will evaluate the general safety profile of therapy with anakinra, 100 mg QD, in subjects with RA after vaccination with a tetanus and diphtheria toxoids injection.

NCT ID: NCT00111462 Completed - Cancer Clinical Trials

Evaluating Treatment of Anemia in Subjects With Non-Myeloid MalignanciesReceiving Multicycle Chemotherapy

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

The purpose of this study is to compare the effect of darbepoetin alfa administered in a weight based versus fixed dosing for the treatment of anemia in subjects with non-myeloid malignancies receiving multicycle chemotherapy.

NCT ID: NCT00111605 Completed - HIV Infections Clinical Trials

Study of an HIV Preventive Vaccine Given With or Without an Adjuvant in HIV Uninfected Adults

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

The purpose of this study is to evaluate the safety and tolerability of an experimental HIV vaccine. The vaccine will be given with or without IL-12 DNA adjuvant (at three escalating doses of 100, 500, and 1,500 mcg respectively), a substance that helps the body respond to a vaccine. This study will also determine the safety and tolerability of an experimental HIV vaccine boosted with two adjuvants.

NCT ID: NCT00111943 Completed - HIV Infections Clinical Trials

Safety and Acceptability of a Vaginal Microbicide

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

The purpose of this study is to determine the safety and acceptability of a vaginal microbicide in HIV uninfected sexually active women. Study hypothesis: The vaginal microbicide 1% tenofovir will be safe and well tolerated in HIV uninfected women who are in good general health.

NCT ID: NCT00113776 Completed - Colorectal Cancer Clinical Trials

Evaluating ABX-EGF Extended Therapy in Subjects With MetastaticColorectal Cancer

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

The purpose of this study is to examine the safety of ABX-EGF administered as monotherapy in subjects with metastatic colorectal cancer who were previously randomized to best supportive care (BSC) in protocol 20020408 and subsequently determined to have progressive disease.

NCT ID: NCT00113958 Completed - Clinical trials for End Stage Renal Disease

Cinacalcet Study to Reach Kidney Disease Outcomes Quality Initiative (K/DOQI) Levels

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

The purpose of this study is to observe the effects of a treatment strategy that incorporates cinacalcet HCl into the management of secondary hyperparathyroidism (HPT) to K/DOQI recommended targets in subjects with end stage renal disease (ESRD) receiving hemodialysis, on bio-intact parathyroid hormone, corrected serum calcium, serum phosphorus, and calcium phosphorus product.

NCT ID: NCT00115414 Completed - Breast Cancer Clinical Trials

Same Day Dosing of Pegfilgrastim in Breast Cancer Patients Undergoing Chemotherapy (TAC)

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

The purpose of this study is to provide data on the safety and efficacy of pegfilgrastim when administered on the same day versus the next day of chemotherapy, as measured by the duration of grade 4 neutropenia.

NCT ID: NCT00115960 Completed - HIV Infections Clinical Trials

Safety of and Immune Response to an HIV Preventive Vaccine (HIV-1 Gag DNA Alone or With IL-15 DNA) Given With or Without 2 Different Booster Vaccinations in HIV Uninfected Adults

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

The purpose of this study is to determine the safety of and immune response to an experimental HIV vaccine, HIV-1 gag DNA, with and without an IL-15 DNA adjuvant (at escalating doses of 100, 500, and 1500 mcg). This study will also test the safety of and immune response to the HIV-1 gag DNA vaccine plus IL-15 DNA adjuvant given with or without 2 other adjuvant-containing booster vaccines.

NCT ID: NCT00116155 Completed - Prostate Cancer Clinical Trials

Trial of IV Injection of CV787 in Hormone Refractory Metastatic Prostate Cancer

Start date: n/a
Phase: Phase 1/Phase 2
Study type: Interventional

This is a multi-center, open-label, dose finding study of CV787 adenovirus in patients with hormone refractory metastatic prostate cancer. Patients will receive treatment intravenously at one of up to nine dose levels, each containing three to six patients.

NCT ID: NCT00117065 Completed - Anemia Clinical Trials

Study of Transplant Related Anemia Treated With Aranesp® (STRATA)

Start date: n/a
Phase: Phase 4
Study type: Interventional

The purpose of this study was to evaluate Aranesp® administered subcutaneously (SC) to maintain hemoglobin (Hb) levels in renal transplant recipients.