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NCT ID: NCT00493532 No longer available - Clinical trials for Postmenopausal Osteoporosis

A Study of Quarterly Intravenous Bonviva (Ibandronate) in Women With Post-Menopausal Osteoporosis.

Start date: June 2007
Phase: Phase 4
Study type: Expanded Access

This single arm study will assess the efficacy and safety of quarterly intravenous Bonviva in women with post-menopausal osteoporosis. All patients will receive Bonviva 3mg i.v. every 3 months. The anticipated time on study treatment is 3-12 months, and the target sample size is 100 individuals.

NCT ID: NCT01026376 No longer available - Clinical trials for Myelodysplastic Syndromes

An Expanded Access Program for Decitabine in Patients With Myelodysplastic Syndrome (MDS)

Start date: June 2008
Phase: Phase 3
Study type: Expanded Access

The purpose of this study is to provide Decitabine to patients with Myelodysplastic syndrome (MDS) of all FAB (French-American-British) subtypes and Intermediate-1, Intermediate-2, and High-Risk International Prognostic Scoring System groups, including both previously treated and untreated patients.

NCT ID: NCT01005537 No longer available - Melanoma (Skin) Clinical Trials

Cyclophosphamide, Autologous Lymphocytes, and Aldesleukin in Treating Patients With Metastatic Melanoma

Start date: June 2009
Phase: N/A
Study type: Expanded Access

RATIONALE: Drugs used in chemotherapy, such as cyclophosphamide, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Biological therapy, such as cellular adoptive immunotherapy using autologous lymphocytes, may stimulate the immune system in different ways and stop tumor cells from growing. Aldesleukin may stimulate the lymphocytes to kill tumor cells. Giving cyclophosphamide together with autologous lymphocytes and aldesleukin may be an effective treatment for metastatic melanoma. PURPOSE: This phase I/II trial is studying the side effects of giving cyclophosphamide together with autologous lymphocytes and aldesleukin and to see how well it works in treating patients with metastatic melanoma.

NCT ID: NCT02297802 No longer available - Clinical trials for Prior Treatment With PD-0325901 With Ongoing Clinical Response

A Single Patient IND for PD-0325901

Start date: June 2013
Phase: Phase 1
Study type: Expanded Access

The purpose of this study is to provide access for a single patient to PD-0325901 who was previously enrolled in a phase I clinical trial.

NCT ID: NCT02142218 No longer available - Clinical trials for Stage III (Unresectable) or Stage IV Advanced Melanoma

Expanded Access Program With Nivolumab to Treat Melanoma

Checkmate 168
Start date: June 2014
Phase: N/A
Study type: Expanded Access

The purpose of this program is to provide treatment with nivolumab to subjects with Stage III or Stage IV advanced melanoma.

NCT ID: NCT01473043 No longer available - Clinical trials for Renal Cell Carcinoma

Clinical Study With Axitinib In Advanced Kidney Cancer, Who Have Failed First Line Treatment

Start date: March 2012
Phase: N/A
Study type: Expanded Access

This is a single arm study with axitinib in patients with advanced kidney cancer (clear cell variant), who have failed first line therapy. The study will recruit a maximum of 30 patients from 2 countries including Australia and Canada. Patients will be followed up for efficacy, safety and health related outcomes.

NCT ID: NCT02026934 No longer available - Clinical trials for Delayed Graft Function

CliniMACS® CD34+ Reagent System for Expanded Access Use

Start date: March 2013
Phase: N/A
Study type: Expanded Access

CliniMACs is an investigational device used to select and enrich stem cells. The device will select the stem cells with CD34+ protein. The participant will be infused with the CD34+ selected cells in the hopes that it will help the participant engraft. Engraftment is when transplanted stem cells resume production of healthy blood cells.

NCT ID: NCT00162188 No longer available - HIV Infection Clinical Trials

An Expanded Access Study of Oral Liquid Efavirenz in the Treatment of Children With HIV Infection: Canada

Start date: May 2001
Phase: N/A
Study type: Expanded Access

This study is being conducted to assess the safety and tolerability of an oral liquid solution of Sustiva for antiretroviral therapy-naive or therapy-experienced HIV-1 infected children between the ages of 3-16 who are failing or intolerant of their current antiretroviral regimen and who are unable to swallow Sustiva capsules.

NCT ID: NCT00046345 No longer available - HIV Infections Clinical Trials

Atazanavir for HIV Infected Individuals: An Early Access Program

Start date: May 2002
Phase: N/A
Study type: Expanded Access

The purpose of this clinical research study is to provide atazanavir to patients infected with human immunodeficiency virus (HIV) whose antiviral medications are no longer working to control HIV activity within the body and who are unable to create a new treatment regimen using other available anti-HIV drugs, because of either side effects or treatment failure previously taken. The safety of this treatment will also be studied.

NCT ID: NCT01378546 No longer available - Clinical trials for Lambert Eaton Myasthenic Syndrome (LEMS)

Treatment of Lambert-Eaton Myasthenic Syndrome (LEMS) With 3, 4 DAP

Start date: May 2005
Phase: N/A
Study type: Expanded Access

Lambert Eaton Myasthenic Syndrome (LEMS) is rare neurological disorder that results in muscle weakness and limited reflex activity. More than half of LEMS cases are associated with a malignancy, usually small cell lung cancer, and tend to progress more quickly than cases not coupled with malignant cells. 3,4diaminopyridine (3,4DAP)is a drug that has been demonstrated to be effective in treating the weakness associated with LEMS as it increases strength and improves autonomic symptoms in LEMS patients. It is not currently approved by the FDA for use in the United States. The investigators plan to use 3,4DAP to treat patients with LEMS here at the Columbia University MDA/ALS Research Center.