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

  NCT02955446

  Conditions:   Neoplasm;   Desmoid Tumor
  Intervention:   Drug: PF-03084014
  Sponsors:   University of Colorado, Denver;   SpringWorks Therapeutics, Inc.
  No longer available
• CTL019 Out of Specification MAP for ALL or DLBCL Patients

  NCT03601442

  Conditions:   Acute Lymphoblastic Leukemia (ALL);   Diffuse Large B-cell Lymphoma (DLBCL)
  Intervention:   Biological: CTL019
  Sponsor:   Novartis Pharmaceuticals
  Available
• Expanded Access Program to Provide Treatment With Pitolisant to Adult Patients in the U.S. With Excessive Daytime Sleepiness Associated With Narcolepsy With or Without Cataplexy

  NCT03433131

  Conditions:   Narcolepsy Without Cataplexy;   Narcolepsy With Cataplexy
  Intervention:   Drug: Pitolisant
  Sponsor:   Harmony Biosciences, LLC
  No longer available
• Midostaurin Access Program for Newly Diagnosed FLT3 (ITD or TKD) Mutated AML Adult Patients Eligible for Standard Induction and Consolidation Chemotherapy

  NCT02624570

  Conditions:   Acute Myeloid Leukemia (AML) With;   FLT3 Mutation, Internal Tandem Duplication (ITD) or Tyrosine Kinase Domain (TKD)
  Intervention:   Drug: Midostaurin
  Sponsor:   Novartis Pharmaceuticals
  Available
• This Record Contains Information About the Mepolizumab Compassionate Use (CU) Product Activities: 104317: CU and Long-Term Access Study of Mepolizumab in HES. 201956:A Long-term Access Programme for Subjects With Severe Asthma 112562: Expanded Access for Patients With Hypereosinophilic

  NCT00244686

  Condition:   Hypereosinophilic Syndrome
  Intervention:   Drug: Mepolizumab
  Sponsor:   GlaxoSmithKline
  Available
• A Facilitated Access Program to Provide Everolimus (RAD) Maintenance for Patients Completing Therapy in RAD Trials in Solid Organ Transplantation

  NCT00149981

  Condition:   Organ Transplantation
  Intervention:   Drug: everolimus (RAD)
  Sponsor:   Novartis Pharmaceuticals
  No longer available
• An Expanded Access Program of Emicizumab in Participants With Hemophilia A With Inhibitors

  NCT03154437

  Condition:   Hemophilia A
  Intervention:   Biological: Emicizumab
  Sponsor:   Genentech, Inc.
  Approved for marketing
• Crizotinib (Xalkori) Expanded Access Protocol For The Treatment Of Adult Or Pediatric Patients

  NCT02473497

  Condition:   Neoplasm
  Intervention:   Drug: Crizotinib
  Sponsor:   Pfizer
  Available
• Expanded Access Protocol - Blinatumomab in Pediatric & Adolescent Subjects With Relapsed/Refractory B-precursor ALL

  NCT02187354

  Condition:   Relapsed/Refractory B-Precursor Acute Lymphoblastic Leukemia
  Interventions:   Drug: Blinatumomab;   Other: Extension of LTFU as per ProtocolAmendment7 7Jun18
  Sponsor:   Amgen
  No longer available
• Expanded Access Study of Gilteritinib (ASP2215) in Patients With FMS-like Tyrosine Kinase 3 (FLT3) Mutated Relapsed or Refractory Acute Myeloid Leukemia (AML) or FLT3-Mutated AML in Complete Remission (CR) With Minimal Residual Disease (MRD)

  NCT03070093

  Conditions:   Acute Myeloid Leukemia (AML);   FMS-like Tyrosine Kinase-3 (FLT3) Mutations
  Intervention:   Drug: gilteritinib
  Sponsor:   Astellas Pharma Global Development, Inc.
  Available
• An Expanded Access Program of Ruxolitinib for the Treatment of Graft-Versus-Host Disease Following Allogeneic Hematopoietic Stem Cell Transplant

  NCT03147742

  Condition:   Graft-versus-host Disease (GVHD)
  Intervention:   Drug: Ruxolitinib
  Sponsor:   Incyte Corporation
  Available
• An Intermediate Access Protocol for Selumetinib for Treatment of Neurofibromatosis Type 1

  NCT03259633

  Condition:   NF type1 With Inoperable Plexiform Neurofibromas
  Intervention:   Drug: Selumetinib
  Sponsor:   AstraZeneca
  Available
• An Open-label Treatment Protocol for VTS-270 in Patients With Neurologic Manifestations of NPC

  NCT03643562

  Condition:   Niemann-Pick Type C Disease
  Intervention:   Drug: VTS270
  Sponsor:   Vtesse, Inc., a Mallinckrodt Pharmaceuticals Company
  Available
• Early Access Treatment With Daratumumab for (Relapsed or Refractory) Multiple Myeloma

  NCT02477891

  Condition:   Multiple Myeloma
  Intervention:   Drug: Daratumumab
  Sponsor:   Janssen Research & Development, LLC
  Approved for marketing
• An Open Label Treatment Use Protocol for Ibrutinib in Subjects With Relapsed or Refractory Mantle Cell Lymphoma

  NCT01833039

  Condition:   Relapsed or Refractory Mantle Cell Lymphoma
  Intervention:   Drug: Ibrutinib
  Sponsors:   Janssen Biotech, Inc.;   Pharmacyclics LLC.
  Approved for marketing