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Studienakronym |
Krankheitsentität  |
Vollständiger Titel / Beschreibung |
Status |
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025/05 |
Bösartige Neubildung des Pankreas
[C25.-]
|
Gemcitabin/Cisplatin in Kombination mit Hyperthermie für Patienten mit lokal fortgeschrittenem oder abdominell metastasiertem Pankreaskarzinom als Zweitlinientherapie nach adjuvanter oder firstline Chemotherapie mit Gemcitabin oder Gemcitabin-Kombination.
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 |
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1/1996 MCP vs CHOP (Hiddemann-Studie) |
Lymphome
[-]
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Therapie von Keimzentrumslymphomen (centroblastisch-centrozytischen L.), Mantelzelllymphomen (centrocytischen L.) und lymphoblasmocytischen Lymphomen in fortgeschrittenen Stadien.
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 |
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114-NH-301 |
Bösartige Neubildungen des lymphatischen, blutbildenden und verwandten Gewebes, als primär festgestellt oder vermutet
[C81-C96]
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A phase III, randomized, double-blind study of galiximab in combination with rituximab compared with rituximab in combination with placebo for the treatment of subjects with relapsed or refractory, follicular Non Hodgkin's lymphoma.
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16349 BAY 80-6946 |
Sonstige und nicht näher bezeichnete Typen des Non-Hodgkin-Lymphoms
[C85.-]
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Phase II PI3K inhibitor in relapsed, indolent or aggressive NHL
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26866138-MMY-2045 |
Multiples Myelom
[C90.0-]
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A Phase 2, Multicentre, Randomised, Open-Label, Parallel Group Study to Evaluate the Safety and Efficacy of VELCADE in combination with Dexamethasone or VELCADE in Combination with Dexamethasone and Cyclophosphomide or VELCADE in combination with Dexamethasone and Lenalidomide ind Subjects with Multiple Myeloma who are Refractory to or Have Relapsed / progressed after Primary Therapy for Multiple Myeloma and have achieved stable disease after 4 cycles of VELCADE/Dexamethasone therapy
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26866138MMY2031 |
Multiples Myelom
[C90.0-]
|
Klinische Prüfung zur Remissionsinduktion mit Bortezomib (Vel.), Cyclophosphamid (C) und Dexamethason (D) bei Patienten bis 60 Jahren mit unbehandeltem Multiplen Myelom und geplanter Hochdosischemotherapie: (VelCD), (DSMM XIA)
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26866138MMY3012 |
Multiples Myelom
[C90.0-]
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Bortezomib in der Konsolidierungstherapie bei Patienten im Alter von < 60 Jahren mit Multiplem Myelom
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26866138MMY3013 |
Multiples Myelom
[C90.0-]
|
Bortezomib in der Konsolidierungstherapie bei Patienten im Alter von 61-75 Jahren mit Multiplem Myelom
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26866138MMY3022 |
Multiples Myelom
[C90.0-]
|
Randomized Phase III Study on Bortezomib and Low-Dose Dexamethasone with or without Continous Low-Dose Oral Cyclophosphamide for Primary Refractory or Relapsed Multiple Myeloma
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A 8851009 |
Aspergillose
[B44.-]
|
A PROSPECTIVE, RANDOMIZED TRIAL COMPARING THE EFFICACY OF ANIDULAFUNGIN AND VORICONAZOLE IN COMBINATION TO THAT OF VORICONAZOLE ALONE WHEN USED FOR PRIMARY THERAPY OF PROVEN OR PROBABLE INVASIVE ASPERGILLOSIS
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 |
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A4061028 |
Bösartige Neubildung des Pankreas
[C25.-]
|
Eine randomisierte, doppelblinde Phase III Studie mit Gemcitabin plus AG-013736 versus Gemcitabin plus Placebo als first-line Therapie bei Patienten mit lokal fortgeschrittenem, nicht resezierbaren oder metastasiertem Pankreaskarzinom
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|
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A536-05 |
Myelodysplastisches Syndrom, nicht näher bezeichnet
[D46.9]
|
An Open-Label Extension Study to Evaluate the Long-Term Effect of ACE-536 for the Treatment of Anemia in Patients with Low or Intermediate-1 Risk Myelodysplastic Syndromes (MDS) Previosly Enrolled in Study A536-03 Z-Nummer: 304
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A61811112 |
GIST
[C15-C19]
|
A phase IIIB, randomized, active controlledopen-labeled study of Sunitinib 37,5 mg daily vs. Imatinib 800 mg daily in the treatment of patients with GIST who havehad PD while on 400 mg daily of Imatinib
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AATT |
Reifzellige T/NK-Zell-Lymphome
[C84.-]
|
Autologous or allogeneic transplantation
following conventional chemotherapy
in younger patients (18-60 yrs.)
with mature (peripheral) T-cell lymphoma
DSHNHL 2006-1A
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AB04030 Masitinib GIST |
Bösartige Neubildung des Rektums
[C20]
Dünndarm, nicht näher bezeichnet
[C17.9]
Kolon, nicht näher bezeichnet
[C18.9]
Magen, nicht näher bezeichnet
[C16.9]
Ösophagus, nicht näher bezeichnet
[C15.9]
|
A prospective, multicenter, randomized, open-label, active-controlled, 2-parallel group, phase III study to compare efficacy and safety of masitinib at 7.5 mg/kg/day to imatinib at 400 or 600 mg in treatment of patients with gastro-intestinal stromal tumour in first line medical treatment
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AB11002 |
Bösartige Neubildung sonstiger und ungenau bezeichneter Verdauungsorgane
[C26]
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A prospective, multicenter, randomised, open-label, activecontrolled, two-parallel groups, phase 3 study to compare the efficacy and safety of masitinib to sunitinib in patients with gastrointestinal stromal tumor after progression with imatinib at 400mg as first line treatment
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AbbVie M12-914 (brocade-3) |
Brustdrüse, nicht näher bezeichnet
[C50.9]
|
A Phase III Randomized, Placebo-Controlled Trial of Carboplatin and Paclitaxel with or without the PARP Inhibitor Veliparib (ABT-888) in Metastatic or Locally Advanced Unresectable BRCA-Associated Breast Cancer
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AbbVIe M14-011 (Brightness) |
Brustdrüse, nicht näher bezeichnet
[C50.9]
|
A Randomized, Placebo-Controlled, Double-Blind Phase III Study Evaluating the Safety and Efficacy of the Addition of a PARP Inhibitor Plus Carboplatin Versus the Addition of Carboplatin in Combination with Standard Neoadjuvant Chemotherapy Versus Standard Neoadjuvant Chemotherapy in Subjects with Early Stage Triple Negative Breast Cancer (TNBC)
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AC220-007 |
Akute myeloblastische Leukämie [AML]
[C92.0-]
|
A PHASE 3 OPEN-LABEL RANDOMIZED STUDY OF QUIZARTINIB (AC220)MONOTHERAPY VERSUS SALVAGE CHEMOTHERAPY IN SUBJECTS WITH FLT3-ITD POSITIVE ACUTE MYELOID LEUKEMIA (AML) REFRACTORY TO OR RELAPSED AFTER FIRST-LINE TREATMENT WITH OR WITHOUT HEMATOPOIETIC STEM CEL
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ACCEPT |
Bösartige Neubildung des Pankreas
[C25.-]
|
Gemcitabine in Combination with the Oral Irreversible ErbB Inhibitor Afatinib versus Gemcitabine Alone in Patients with Metastatic Pancreatic Cancer: an Explorative Randomized Phase II Trial
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ACCEPT |
Pankreas Karzinom
[C25.0]
|
Gemcitabine in combination with the oral irreversible ErbB Inhibitot Afatinib versus Gemcitabine alone in patients with metastatic pancreatic cancer: an explorative randomized phase II trial
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ACCRA-HN |
HNO-Tumor
[C00-C14, C30.-,C33]
|
Multizentrische, offene Phase II-Studie zur Strahlentherapie in Kombination mit einer Chemotherapie und einer Antikörper-Therapie nach erfolgter Operation von fortgeschrittenen Karzinomen der Mund- oder Rachenhöhle (nur noch Follow up)
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ACE-536-MDS-001 |
Myelodysplastisches Syndrom, nicht näher bezeichnet
[D46.9]
|
A Phase 3, Double-blind, Randomized Study to Compare the Efficacy and Safety of Luspatercept (ACE-536) Versus Placebo for the Treatment of Anemia Due to IPSS-R Very Low, Low, or Intermediate Risk Myelodysplastic Syndromes in Subjects with Ring Sideroblasts Who Require Red Blood Cell Transfusions,
|
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ACE-536-MDS-002 (COMMANDS) |
Myelodysplastisches Syndrom, nicht näher bezeichnet
[D46.9]
|
A PHASE 3, OPEN-LABEL, RANDOMIZED STUDY TO COMPARE THE EFFICACY AND SAFETY OF LUSPATERCEPT (ACE-536) VERSUS EPOETIN ALFA FOR THE TREATMENT OF ANEMIA DUE TO IPSS-R VERY LOW, LOW OR INTERMEDIATE RISK MYELODYSPLASTIC SYNDROMES (MDS) IN ESA NAÏVE SUBJECTS WHO REQUIRE RED BLOOD CELL TRANSFUSIONS, The “COMMANDS” Trial
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|
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ACE-LY-308 |
Mantelzell-Lymphom
[9673/3]
|
A Phase 3, Randomized, Double-blind, Placebo-controlled, Multicenter Study of Bendamustine and Rituximab (BR) Alone Versus in Combination with Acalabrutinib (ACP-196) in Subjects with Previously Untreated Mantle Cell Lymphoma
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