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NCT ID: NCT00091741 Completed - HIV Infection Clinical Trials

Safety and Efficacy Study of Etanercept (Enbrel) on the Response Rate of HIV-infected Subjects

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

The purpose of conducting this already-FDA approved Phase I clinical trial is to evaluate the safety and efficacy of etanercept (Enbrel) on the response rate in HIV-infected subjects who have failed to respond to conventional antiretroviral (HAART) therapy and for whom no alternative therapy exists. The greatest challenge faced by HIV-treating clinicians today is the management of virologic failure and metabolic complications of anti-HIV treatment. Treatment failure can occur because of non-compliance, drug discontinuation, lack of drug potency, inadequate drug plasma concentration or drug resistance. Of these, drug resistance remains the single most important reason for virological failure and rapidly limits treatment options.

NCT ID: NCT00092911 Completed - Depression Clinical Trials

Study Evaluating DVS-233 SR in Adult Outpatients With Major Depressive Disorder

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

The main objective of this study is to compare the antidepressant efficacy and safety of DVS-233 SR versus placebo in adult outpatients with Major Depressive Disorder.

NCT ID: NCT00092924 Completed - Clinical trials for Carcinoma, Non-Small-Cell Lung

Study of TRM-1(TRAIL-R1 Monoclonal Antibody) in Subjects With Relapsed or Refractory Non-Small Cell Lung Cancer (NSCLC)

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

The purpose of this study is to evaluate the efficacy and safety of TRM-1 in subjects with relapsed or refractory non-small cell lung cancer.

NCT ID: NCT00093171 Completed - Hemophilia B Clinical Trials

Study Evaluating rFIX; BeneFIX® in Hemophilia B

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

The primary objective of this clinical research study is to assess the safety and efficacy of rFIX for a minimum of 6 months in previously treated patients (PTPs) with hemophilia B (FIX:C ≤2%) during standard-of-care treatment (on-demand, prophylaxis, and through major and minor surgical procedures).

NCT ID: NCT00093210 Completed - Hemophilia B Clinical Trials

Study Evaluating of Recombinant Human Factor IX (BeneFIX) and a New Formulation of BeneFIX (rFIX-R) in Moderate to Severe Hemophilia B

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

The primary objective of this clinical research study is to establish the bioequivalence of 2 treatments, rFIX and rFIX-R, when given as a 10-minute intravenous bolus infusion.

NCT ID: NCT00094640 Completed - Schizophrenia Clinical Trials

Pharmacokinetic Characterization of Intramuscular Olanzapine Depot

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

The goals of this study are to: Determine the blood levels of intramuscular (IM) olanzapine depot in patients at different points in time after an injection, and compare these levels to the amount of olanzapine in the blood of patients after treated by oral administration with Zyprexa (olanzapine) tablets or by intramuscular administration with Zyprexa IntraMuscular (olanzapine for injection).

NCT ID: NCT00095342 Completed - Clinical trials for Rheumatoid Arthritis

Study Evaluating TMI-005 in Active Rheumatoid Arthritis

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

The primary objective of this clinical research study is to compare the efficacy and the safety of 3 dose levels of oral TMI-005 in comparison with placebo in subjects with active Rheumatoid Arthritis (RA) who have been receiving stable doses of Methotrexate (MTX).

NCT ID: NCT00096694 Completed - HIV Infections Clinical Trials

Effect of an Intrauterine Contraceptive Device (IUD) in HIV Infected Women

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

Oral contraceptives (OCs) are not a good option for some HIV infected women because of the potential for drug interactions between OCs and anti-HIV drugs; additionally, OCs may increase the risk of transmitting HIV to sexual partners. Levonorgestrel is commonly prescribed as part of a combination OC. An intrauterine device (IUD) is a device inserted in a woman's uterus to prevent pregnancy. The purpose of this study is to determine the effect of a levonorgestrel-releasing IUD on the amount of HIV present in an HIV infected woman's cervix after 4 weeks of IUD use. Study hypothesis: There will be no increase in genital tract HIV RNA and DNA after placement of the levonorgestrel IUD.

NCT ID: NCT00096837 Completed - Multiple Myeloma Clinical Trials

A Study of Motexafin Gadolinium for the Treatment of Relapsed or Refractory Multiple Myeloma

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

The purpose of the study is to determine if the drug motexafin gadolinium will be an effective treatment for patients who have relapsed or refractory multiple myeloma.

NCT ID: NCT00096850 Completed - HIV Infections Clinical Trials

Safety, Tolerability, and Blood Levels of Ritonavir-Boosted Atazanavir and Rifampin When Taken Together in HIV Uninfected Adults

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

Rifampin (RIF) is used for the treatment of tuberculosis (TB), an infectious disease that affects many people with HIV. RIF was shown to lower concentrations and decrease the effectiveness of some anti-HIV drugs, including the HIV protease inhibitor (PI) atazanavir (ATV) boosted with ritonavir (RTV). The purpose of this study is to determine the interactions between RTV-boosted ATV and evaluate the safety and tolerability of giving these drugs together in HIV uninfected adults.