Clinical Trials Logo

Filter by:
NCT ID: NCT01779518 Approved for marketing - Clinical trials for Post-transplant Hepatitis C

Expanded Access Program of Sofosbuvir With Ribavirin and With or Without Pegylated Interferon in Aggressive Post-transplant Hepatitis C

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

This is a single arm, open-label study which will be opened at specific clinical sites at the request of an investigator for the treatment of individual subjects for whom there are no other treatment options. Subjects will be treated for 24 weeks with sofosbuvir (400mg QD) with RBV; pegylated interferon may be added at the discretion of the investigator.

NCT ID: NCT01825395 Approved for marketing - Clinical trials for Lambert Eaton Myasthenic Syndrome

Use of 3,4-Diaminopyridine in the Treatment of Lambert-Eaton Syndrome

3 4-DAP
Start date: n/a
Phase:
Study type: Expanded Access

To learn more about the effect of 3, 4-Diaminopyridine (3,4-DAP) on patient diagnosed with Lambert-Eaton myasthenic syndrome (LEMS).

NCT ID: NCT01833039 Approved for marketing - Clinical trials for Relapsed or Refractory Mantle Cell Lymphoma

An Open Label Treatment Use Protocol for Ibrutinib in Subjects With Relapsed or Refractory Mantle Cell Lymphoma

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

The purpose of this study is to provide patients who have relapsed or refractory Mantle Cell Lymphoma (MCL) with early access to an investigational medication called ibrutinib (PCI-32765) and to collect safety information about the drug.

NCT ID: NCT01858103 Approved for marketing - MPS IVA Clinical Trials

BMN 110 US Expanded Access Program

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

The Expanded Access Program (EAP) is an open-label, multicenter program to: 1. Provide patients who have been diagnosed with Mucopolysaccharidosis IVA (MPS IVA) access to BMN 110 until commercial product is available 2. Collect additional information on the safety and tolerability of BMN 110 administration in patients with MPS IVA Patients enrolled in the EAP will receive 2.0 mg/kg intravenous infusions of BMN 110 every week during the program.

NCT ID: NCT01861834 Approved for marketing - Clinical trials for Cholestasis of Parenteral Nutrition

Safer Parenteral Nutrition in Pediatric Short Bowel Syndrome to Decrease Liver Damage

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

To provide children dependent on total parenteral nutrition with Omegaven®, a fish oil-based intravenous lipid emulsion that may be less hepatotoxic than conventional, vegetable oil-based intravenous lipid emulsions, and that may therefore reduce the need for liver transplantation.

NCT ID: NCT01869803 Approved for marketing - Clinical trials for Recurrent Adult Acute Myeloid Leukemia

Gemtuzumab Ozogamicin in Treating Patients With Relapsed or Refractory Acute Myeloid Leukemia or Acute Promyelocytic Leukemia

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

This clinical trial studies gemtuzumab ozogamicin in treating patients with relapsed or refractory acute myeloid leukemia or acute promyelocytic leukemia. Monoclonal antibodies, such as gemtuzumab ozogamicin, can block cancer growth in different ways. Some block the ability of cancer to grow and spread. Others find cancer cells and help kill them or carry cancer-killing substances to them.

NCT ID: NCT01931306 Approved for marketing - Clinical trials for Carcinoma, Non-Small-Cell Lung

Expanded Access Study of Afatinib in Treatment-naive or Chemotherapy Pre-treated Patients With Non-small Cell Lung Cancer (NSCLC)

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

To provide expanded access and to evaluate the safety, tolerability and efficacy of afatinib in patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) harboring Epidermal Growth Factor Receptor (EGFR) mutation(s) and have never been treated with an EGFR tyrosine kinase inhibitor (TKI)

NCT ID: NCT01983722 Approved for marketing - Dravet Syndrome Clinical Trials

Treatment Plan to Provide Expanded Access to Stiripentol for Patients With Dravet Syndrome

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

Expanded access to Stiripentol for patients with Dravet Syndrome.

NCT ID: NCT01995734 Approved for marketing - Acromegaly Clinical Trials

An Open-label, Multi-center, Expanded Treatment Protocol of Pasireotide LAR in Patients With Acromegaly

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

The present study is planned as an expanded treatment protocol to provide acromegalic patients for whom medical therapy is appropriate access to pasireotide LAR while regulatory approval for pasireotide is sought.

NCT ID: NCT02136511 Approved for marketing - Clinical trials for Chronic Lymphocytic Leukemia (CLL)

Expanded Access for Idelalisib in Combination With Rituximab in Chronic Lymphocytic Leukemia

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

This study is to provide idelalisib (IDELA) to individuals with relapsed, previously treated chronic lymphocytic leukemia (CLL) who have limited treatment options and are not eligible for other Gilead-sponsored studies.