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NCT ID: NCT01309022 No longer available - Clinical trials for Diabetes Mellitus, Type 1

Immunosuppressive Medications for Participants in ITN005CT (NCT00014911)

Start date: n/a
Phase: N/A
Study type: Expanded Access

The purpose of this protocol is to provide continued acess to immunosuppressive medications to subjects from the completed/closed trial ITN005CT (NIS01,NCT00014911). THIS PROTOCOL DOES NOT PROVIDE MEDICINES TO DIABETES PATIENTS WHO DID NOT PARTICIPATE IN ITN005CT.

NCT ID: NCT01317082 No longer available - Nausea Clinical Trials

Use of the Pressure Right Device After Laparoscopic Surgery

Start date: n/a
Phase: N/A
Study type: Expanded Access

The primary objective is to test the hypothesis that the use of the Pressure Right device in combination with ondansetron and dexamethasone would result in a lower incidence of postoperative vomiting (emesis) than the combination of antiemetic therapy alone.

NCT ID: NCT01370447 No longer available - Clinical trials for Mitochondrial Diseases

EPI-743 for Mitochondrial Respiratory Chain Diseases

Start date: n/a
Phase:
Study type: Expanded Access

This study will evaluate the safety and efficacy of EPI-743 in participants with severe mitochondrial respiratory chain diseases who are considered to be within 90 days of end-of-life care.

NCT ID: NCT01374282 No longer available - Scleroderma Clinical Trials

Post Marketing Surveillance Study of Cuprimine

Start date: n/a
Phase: N/A
Study type: Expanded Access

Cuprimine (penicillamine) was made available in the Philippines by the Sponsor under a Compassionate Special Permit issued by the Bureau of Food and Drugs. Physicians were able to request the drug for their patients from the Sponsor. A Clinical Study Report form was completed for each purchase of Cuprimine.

NCT ID: NCT01384773 No longer available - Keratoconus Clinical Trials

Progressive Keratoconus or Ectasia Treatment Plan

Start date: n/a
Phase:
Study type: Expanded Access

Keratoconus and pellucid marginal degenerations are genetically based ocular conditions and post surgical ectasia is an iatrogenic condition. These diseases are characterized by weakening of the front part of the eye that causes thinning and distortion. This distortion results in unevenness of the cornea and produces progressive near-sightedness and irregularity, which causes loss of vision when using eyeglasses. When eyeglasses fail to give enough vision, the the investigators use rigid contact lenses to create an artificial front eye surface. This improves visual acuity in many patients although they eventually fail either because they cannot be tolerated or the surface irregularity has become so severe that they are rejected. At this stage there is usually thinning and loss of clarity of the eye. There has been no treatment for this other than corneal transplantation, a complex surgical procedure with a significant complication rate and a delay in visual recovery. The treatment the investigators wish to perform strengthens the front of the eye by a chemical reaction using light and riboflavin. This technique has been studied over a decade and is widely used throughout the world. The FDA approved multicenter American clinical study is being analyzed in anticipation of its submission to the FDA for PreMarket approval. Because this is a progressive condition, the investigators wish to be able to offer this on a limited basis to patients in need with vision loss. Any treatment that can delay or prevent corneal transplantation is of great benefit. The investigators believe the evidence is compelling that this treatment is the sole alternative to surgical transplantation.

NCT ID: NCT01427582 No longer available - Soft Tissue Sarcoma Clinical Trials

YONDELIS (Trabectedin) Single Patient Compassionate Use / Expanded Access

Start date: n/a
Phase: N/A
Study type: Expanded Access

The YONDELIS (trabectedin) Single Patient Compassionate Use /Expanded Access program provides patients with advanced soft tissue sarcoma, who do not qualify for ongoing clinical trials with YONDELIS (trabectedin), access to this investigational treatment.

NCT ID: NCT01432483 No longer available - Cancer Clinical Trials

Access Program With Denileukin Diftitox for the Treatment of Patients Currently Receiving Treatment With Commercially Available (Ontak)

Start date: n/a
Phase: N/A
Study type: Expanded Access

The purpose of this study is to provide continued therapy with Denileukin diftitox (ONTAK) to patients who are currently on therapy and who have no other suitable treatment options, where therapy is requested by their physician.

NCT ID: NCT01435551 No longer available - Alzheimer Disease Clinical Trials

Using Hypnotherapy For Dementia & Alzheimer's

Start date: n/a
Phase: N/A
Study type: Expanded Access

From the past research that has been done the investigators have learned that brain cells die & leave a deposit in the brain known as beta-amyloid. Since alzheimer's is a slow acting disease the natural immune system does not respond to this illness so this builds up in the brain. As it builds up it gets into the neurotransmitters in the brain causing more brain cells to die. As these buildups occur dementia sets in due to more of the brain dying & effects normal activity. STUDY WAS CANCELLED Hypnotherapy will be used to do the following things: - Increase the immune system - The immune system will begin to clean up the beta-amyloid buildup - That removes damage cells of the brain - Increase more blood flow to the brain - Allows the active brain cells to be trained to carry out daily activities STUDY WAS CANCELLED

NCT ID: NCT01461304 No longer available - Barth Syndrome Clinical Trials

Compassionate Use of Triheptanoin (C7) for Inherited Disorders of Energy Metabolism

Start date: n/a
Phase:
Study type: Expanded Access

This is a compassionate use study to allow patients already taking triheptanoin (C7) through previous studies to continue to receive the supplement. It will also allow triheptanoin supplementation in patients with qualifying disorders if they are failing conventional therapy.

NCT ID: NCT01508286 No longer available - Hepatitis C Clinical Trials

Early Access Program of Telaprevir With Peginterferon and Ribavirin in Chronic Hepatitis C Subjects

Start date: n/a
Phase: Phase 3
Study type: Expanded Access

The purpose of this early access program is to provide telaprevir to patients with a specific type of hepatitis C viral infection (termed 'genotype 1') who are expected to benefit from telaprevir-based therapy but who reside in countries in which telaprevir is not yet commercially available and who are not eligible for enrollment into a clinical study of telaprevir. The study also aims to collect information on the safety and adverse events with telaprevir treatment in combination with peginterferon alfa and ribavirin, which is typically used to treat patients with hepatitis C. In addition to hepatitis C viral infection, patients in this study will also have a diagnosis of liver fibrosis and compensated liver disease.