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NCT ID: NCT03134131 No longer available - Glioma Clinical Trials

Expanded Access to ONC201 for Patients With H3 K27M-mutant and/or Midline High Grade Gliomas

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

The objective of this expanded access program is to provide ONC201 to eligible patients with previously-treated glioma that exhibits the H3 K27M mutation and/or that is located in the midline region of the brain.

NCT ID: NCT03125486 No longer available - Clinical trials for Systemic Lupus Erythematosus

Compassionate Use for Subcutaneous (SC) Belimumab

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

GlaxoSmithKline (GSK) have submitted a Biologic License Application (BLA) for the subcutaneous formulation of belimumab which is currently under review by the Food and Drug Administration (FDA). The goal of this individual patient compassionate use supply is to provide a patient with subcutaneous belimumab for the period of 1 year or until the subcutaneous formulation of belimumab becomes approved for use by the FDA and is commercially available to this patient, whichever is sooner. You can access GSK's Policy on Compassionate via http://www.gsk.com/media/3368/compassionate-use.pdf.

NCT ID: NCT03066661 No longer available - Clinical trials for Cancers With NTRK, ROS1, or ALK Gene Fusions

Expanded Access to Entrectinib for Cancers With NTRK1/2/3, ROS1, or ALK Gene Fusions

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

Expanded access to entrectinib will be given to patients with cancers harboring NTRK1/2/3, ROS1, or ALK gene fusions who do not qualify for participation in, or who are otherwise unable to access, an ongoing clinical trial for entrectinib.

NCT ID: NCT03062631 No longer available - Clinical trials for Congenital Myasthenic Syndrome

Treatment Use of 3,4 Diaminopyridine in Congenital Myasthenia

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

Congenital myasthenia is a potentially lethal disorder, which, even with careful management, significantly impedes participation in normal daily functions. Currently approved therapies have had little impact on promoting a normal quality of life activity in these patients. The goal is to systematically examine the effect of 3,4-DAP on the natural course of this disease and to gain additional experience in titrating 3,4-DAP with other available therapies to maximize clinical function and development in this patient population. The specific aim of this study is to evaluate the use of 3,4 Diaminopyridine (DAP) on selected patients proven by genetic or serum antibody testing to have Congenital Myasthenic Syndrome (CMS), prescribe 3,4 DAP, and then clinically evaluate the response.

NCT ID: NCT03052569 No longer available - Clinical trials for Cancers With RET Alterations

Expanded Access to RXDX-105 for Cancers With RET Alterations

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

Expanded access to RXDX-105 will be given to patients with cancers harboring RET alterations who have not received TKIs that target RET alterations, who do not qualify for participation in, or who are otherwise unable to access, an ongoing clinical trial for RXDX-105.

NCT ID: NCT02985658 No longer available - Clinical trials for Triple-Negative Breast Cancer

Expanded Access With ABT-888 (Veliparib) to Treat Metastatic Breast Cancer

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

This is an expanded access protocol to allow continued maintenance therapy with ABT-888 (veliparib) for three patients with metastatic triple negative breast cancer who are currently receiving the investigational product in association with clinical trial participation. Additionally, the protocol will enroll up to 7 new patients with metastatic BRCA associated or triple negative breast cancer to allow for additional access to veliparib monotherapy, or at the investigator's discretion, veliparib in combination with cisplatin and/or vinorelbine.

NCT ID: NCT02968953 No longer available - Clinical trials for Glucose Transporter 1 Deficiency Syndrome

Treatment With UX007 for a Single Patient With GLUT1 Deficiency Syndrome

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

This treatment plan is intended for the use of UX007 (triheptanoin) in the treatment of a single patient with Glucose Transporter 1 (GLUT1) Deficiency Syndrome.

NCT ID: NCT02960620 No longer available - Clinical trials for HepatoCellular Carcinoma

Therasphere for Unresectable Primary or Secondary Liver Neoplasia

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

This is not a research study. The purpose is to provide supervised access to TheraSphere® therapy at this institution.

NCT ID: NCT02955446 No longer available - Neoplasm Clinical Trials

Compassionate Use Protocol for PF-03084014 in Patients With Advanced Solid Tumor Malignancies

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

This is a single-center, open label, non randomized, compassionate use protocol in patients with advanced solid tumor malignancies who were previously enrolled in the phase I study (NCT00878189) of this agent.

NCT ID: NCT02925520 No longer available - Clinical trials for Parenteral Nutrition-Associated Liver Disease

Expanded Access Use of Omegaven® in the Treatment of Parenteral Nutrition Induced Liver Injury in Children

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

This is an expanded access study to assess the safety profile and changes in serum direct bilirubin levels in infants with PN associated cholestasis. Eligible patients will receive therapy with Omegaven on an expanded access basis by method of continuous infusion. Omegaven will be infused intravenously through either a central or peripheral catheter in conjunction with parenteral nutrition. The same standards of care provided to all patients receiving parenteral nutrition solution will be followed.