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Genetic Diseases, X-Linked clinical trials

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NCT ID: NCT01289847 Completed - Clinical trials for Common Variable Immunodeficiency

A Study to Find Out How Safe and Effective Gammaplex® is in Young People With Primary Immunodeficiency

Start date: March 2011
Phase: Phase 4
Study type: Interventional

The main objective is to determine the efficacy of Gammaplex by measuring the number of serious acute bacterial infections during treatment with Gammaplex over a 12 month period. The secondary objectives are to assess the safety and tolerability of Gammaplex and to compare the data collected from adult subjects with PID from the GMX01 study

NCT ID: NCT01108068 Completed - Clinical trials for Osteoporosis Pseudoglioma

Trial of Lithium Carbonate for Treatment of Osteoporosis-pseudoglioma Syndrome

Start date: July 2010
Phase: N/A
Study type: Interventional

This was a pilot study of 10 patients with Osteoporosis-pseudoglioma syndrome (OPPG) from the Old Order Mennonite community and 16 controls, who did not have OPPG. Five of the 10 OPPG patient elected to participate in the Lithium trial and 5 participated only in baseline data (labs, pQCT). The 5 with OPPG who were given lithium for 6 months had both dual energy xray absorptiometry (DXA), peripheral quantitative computerized tomography (pQCT) and lab assessment at baseline and 6 months. Studies in the mouse model of OPPG showed that lithium normalized their bone strength. Controls (n=16) were recruited from the Old Order Mennonite community, to minimize the effects of environmental and lifestyle factors. The controls were not be given lithium. The age range of participants was 4-64 years.

NCT ID: NCT00774358 Completed - Clinical trials for Wiskott-Aldrich Syndrome (WAS)

Interleukin-2 Treatment for Wiskott-Aldrich Syndrome

WAS
Start date: October 2008
Phase: Phase 1
Study type: Interventional

Funding Source--FDA OOPD. Orphan Product Grant Number--1R01FD004091-01A1 Context: Wiskott-Aldrich syndrome (WAS) is a fatal, devastating disease with ill-defined treatment modalities, which affects young boys. Classic WAS is characterized by a clinical triad of thrombocytopenia, eczema and severe, recurrent infections. Despite diagnostic and therapeutic advances most WAS patients die at less than 12 years of age due to infections, hemorrhage, malignancy or complications from treatments. WAS patients suffer from herpesvirus infections as a result of poor Natural Killer (NK) cell function (cytotoxicity). In the laboratory, the investigators have seen correction of WAS Natural Killer Cell (NK) function after treatment with Interleukin-2 (IL-2). Objectives: Initiate a prospective clinical trial by treating WAS subjects with IL-2 and using safety as the primary endpoint. Restoration of NK cell cytotoxicity and effects on cytoskeletal dynamics are secondary endpoints. The investigators will also observe patient clinical status (eczema, infections, use of treatment dose antibiotics, food allergies, etc). Study Design/Setting/Participants: This is a prospective clinical trial treating 9 WAS subjects in the Clinical Translational Research Center (CTRC) with IL-2. Intervention: The investigators propose to subcutaneously administer 0.5 Million Units (MU)/m2 of IL-2 daily to WAS subjects for 5 days. Research treatment will be repeated 2 and 4 months later. Inter-patient dose escalation will be employed to 1 MU/m2 and/or 2 MU/m2 based on safety as the primary endpoint. Study Measures: The investigators will observe safety and tolerability measures and perform assays on subject blood samples prior to and after research treatment to observe improvement in NK cell function.

NCT ID: NCT00741299 Completed - Bipolar Disorder Clinical Trials

A Study of the Association Between Tobacco Smoking and Bipolar Affective Disorder

Start date: August 2007
Phase: N/A
Study type: Observational

The purpose of this study is to examine whether tobacco smoking is associated with bipolar affective disorder (severity of depressive and manic symptoms, presence of psychotic symptoms, history of a suicide attempts and other clinical features.)

NCT ID: NCT00683709 Completed - Clinical trials for Schizoaffective Disorder

Specialized Clozapine Clinic for Bipolar and Schizoaffective Disorder

Start date: January 2007
Phase: Phase 4
Study type: Observational

Bipolar Disorder (BD) and Schizoaffective Disorder (SA) clients. - determine if after 12 months of treatment with clozapine, the BMI changes with clients who are councelled as usual regarding weight gain while on Clozapine. - determine if after 12 months of treatment with clozapine, the BMI changes with intense, structured councelling about diet and exercise.

NCT ID: NCT00593099 Completed - Bipolar Disorder Clinical Trials

A Preliminary Study of Sustained-Release Bupropion for Smoking Cessation in Bipolar Affective Disorder

Start date: April 2004
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this pilot study is to determine the safety and potential efficacy of sustained-release bupropion (Zyban®) for the treatment of nicotine dependence in patients with bipolar affective illness. It is hypothesized that bupropion will produce a significant enhancement of smoking abstinence compared to placebo and will be safe for use in these patients.

NCT ID: NCT00569023 Completed - Night Blindness Clinical Trials

Treatment of Congenital Stationary Night Blindness With an Alga Containing High Dose of Beta Carotene

Start date: July 2007
Phase: N/A
Study type: Interventional

To assess the effect of oral administration of the alga Dunaliella bardawil containing approximately 50% all-trans beta-carotene and 50% 9-cis beta-carotene isomers on visual functions patients with Congenital Stationary Night Blindness {Fundus albipunctatus).

NCT ID: NCT00542997 Completed - Clinical trials for Common Variable Immunodeficiency

Study of Subcutaneous Immune Globulin in Patients Requiring IgG Replacement Therapy

Start date: September 2007
Phase: Phase 3
Study type: Interventional

The objective of this study is to assess the efficacy, tolerability, safety and pharmacokinetics of IgPro20 in patients with primary humoral immunodeficiency (PID).

NCT ID: NCT00359411 Completed - Clinical trials for Genetic Diseases, X-Linked

Genetic Studies of X-linked Lymphoproliferative Disease

Start date: May 22, 1996
Phase: N/A
Study type: Observational

This study will study the effects of the gene on the X chromosome that is associated with X-linked lymphoproliferative disease (XLPD)-an inherited disease affecting the immune system-on the function of the immune system. XLPD has been linked to an abnormality in a specific region of the X chromosome (one of 23 chromosome pairs that contain the genes that determine a person's hereditary makeup). The disease may develop after infection with the Epstein-Barr virus (EBV). EBV affects more than 95 percent of people in the United States. It usually does not cause any symptoms in children. In adolescents and adults, however, EBV can cause infectious mononucleosis and sometimes lymphoproliferative disease, such as XLPD. In these diseases lymph tissues, such as lymph nodes, may become enlarged and immune function (infection-fighting ability) impaired. This study will compare DNA from patients with XLPD with that of their unaffected relatives, of patients with other lymphoproliferative diseases and of normal controls. Patients of any age with XLPD, their unaffected relatives 18 years of age and older, and patients with other lymphoproliferative diseases may participate in this study. Blood samples will be collected from all participants to study the effects of the gene on the X chromosome that appears to be abnormal in XLPD on the function of the immune system. In a 6-week period, no more than 100 milliliters (about 7 tablespoons) of blood will be drawn from adults and no more than 1 ml (1/6 teaspoon) of blood per pound of body weight from children. Blood from patients with XLPD and their relatives will also be tested for HLA type (similar to blood type testing) and the ability of HLA-matched cells from patients and relatives to interact will be examined.

NCT ID: NCT00278954 Completed - Clinical trials for Primary Immunodeficiency

Efficacy, Safety and Pharmacokinetics of Gammaplex in Primary Immunodeficiency Diseases.

Start date: January 2006
Phase: Phase 3
Study type: Interventional

The main objective of this study is to see if GAMMAPLEX is efficacious with respect to Food and Drug Administration (FDA) minimal requirements (no more than 1 serious, acute, bacterial infection per subject per year) in subjects with Primary Immunodeficiency Diseases (PID). The secondary objectives are to assess the safety and tolerability of GAMMAPLEX and to determine if GAMMAPLEX has a pharmacokinetic (PK) profile comparable with that of intact Immunoglobulin G (IgG) in subjects with PID.