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Studienakronym |
Krankheitsentität  |
Vollständiger Titel / Beschreibung |
Status |
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CA209214 |
Sonstige Tumore
[]
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A Phase 3, Randomized, Open-Label Study of Nivolumab Combined with Ipilimumab Versus Sunitinib Monotherapy in Subjects with Previously Untreated, Advanced or Metastatic RenalCell Carcinoma
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CA209274 |
Sonstige Tumore
[]
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a Phase III, randomized, double-blind, multicenter study of adjuvant Nivolumab versus Placebo in subjects with high risc invasive urothel carcinoma
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CA209275 |
Sonstige Tumore
[]
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A phase II single arm clinical trial of nivolumab (BMS-936558) in subjects with metastatic or unresectable urothelial cancer who have progressed or recurred following treatment with a platinum agent
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CA224-047 |
Krebserkrankungen der Haut
[]
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A Randomized, Double-Blind Phase 2/3 Study of Relatlimab Combined with Nivolumab versus Nivolumab in Participants with Previously Untreated Metastatic or Unresectable Melanoma Z:339
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Cabozantinib |
Prostatakrebs
[]
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A Phase 3, Randomized, Double-blind, Controlled Study of Cabozantinib (XL184) Versus Prednisone in Metastatic Castration-resistant Prostate Cancer Patients Who Have Received Prior Docetaxel and Prior Abiraterone or MDV3100
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CAIN457A2303 |
Psoriasis, nicht näher bezeichnet
[L40.9]
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A randomized, double-blind, placebo controlled, multicenter study of subcutaneous AIN457 to demonstrate efficacy at Week 12 compared to placebo and etanercept and to assess the safety, tolerability and long-term efficacy up to one year in subjects with moderate to severe chronic plaque-type psoriasis.
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CAIN457ADE01T (Secukinomab) |
Pyoderma gangraenosum
[L88]
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Pilotstudie zum Einsatz von anti-IL-17 (Secukinumab) bei der Behandlung von Pyoderma gangraenosum CAIN457ADE01T
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CAIN457FDE03 ASTRUM |
Spondylitis ankylosans
[M45.0-]
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A randomized, double-blind, placebo-corntrolled multicenter study of Secukinumab (AIN457) to examine the clinical efficacy and the NSAID-sparing effect of Secukinumab over 16 weeks in patients with ankylosing Spondylitis (ASTRUM)
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CAMN107DDE05 |
Gastrointestinales Stromasarkom
[8936/3]
Krebs des Verdauungstrakts
[]
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An open-label, multi-center study to evaluate the efficiency of nilotinib in adult patients with GIST tumors resistant to imatinib and sunitinib
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CAMN107DDE06 |
Gastrointestinales Stromasarkom
[8936/3]
Krebs des Verdauungstrakts
[]
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An open label, multi-center, single-arm study to evaluate the efficacy of nilotinib in adult patients with metastatic or unresectable GIST in first line treatment
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CAMN107G2301 |
Gastrointestinales Stromasarkom
[8936/3]
Krebs des Verdauungstrakts
[]
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A randomized, open-label, multi-center phase III study to evaluate the efficacy and safety of nilotinib vs. imatinib in adult patients with unresectable or metastatic GIST
|
 |
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CAO/ARO/AIO-04 |
Tumor des Dickdarms / Mastdarms
[]
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Prospektiv randomisierte, multizentrische Studie der Phase III: Präoperative Radio-/Chemotherapie und adjuvante Chemotherapie mit Capecitabin plus Oxaliplatin im Vergleich zu einer präoperativen Radio-/Chemotherapie und adjuvanten Chemotherapie mit 5-Fluorouracil beim lokal fortgeschrittenen Rektumkarzinom im UICC-Stadium II und III
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CAO/ARO/AIO-04 |
Bösartige Neubildung am Rektosigmoid, Übergang
[C19]
Tumor des Dickdarms / Mastdarms
[]
Krebs des Verdauungstrakts
[]
|
Prospektiv randomisierte, multizentrische Studie der Phase III: Präoperative Radio-/Chemotherapie und adjuvante Chemotherapie mit 5-Fluorouracil plus Oxaliplatin im Vergleich zu einer präoperativen Radio-/Chemotherapie und adjuvanten Chemotherapie mit 5-Fluorouracil beim lokal fortgeschrittenen Rektumkarzinom im UICC-Stadium II und III
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CAPRELSAT |
Bösartige Neubildung der Schilddrüse
[C73]
Schilddrüsentumore
[]
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European, Observational, Prospective Study to Evaluate the Benefit/Risk of Vandetanib in RET Mutation Negative and Positive Patients With Symptomatic, Aggressive, Sporadic, Unresectable, Locally Advanced/Metastatic Medullary Thyroid Cancer
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CARIN-Studie |
Bösartige Neubildung der Brustdrüse [Mamma]
[C50.-]
Brustkrebs
[]
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Verbesserung der Wirksamkeit eines Therapieregime aus Capecitabin und Bevacizumab bei Patientinnen mit metastasiertem oder inoperablem HER2/neu negativem Mammakarzinom durch Zusatz von Vinorelbin.
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Caroline meets HANNA |
Gynäkologische Tumore
[]
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„Caroline meets HANNA – Holistic Analysis of LoNgterm-survival with OvariaN CAncer” Expression VI
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CASSINI |
Sonstige Koagulopathien
[D68.-]
Sonstige Studien
[-]
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Efficacy and Safety of Rivaroxaban Prophylaxis Compared with Placebo in Ambulatory Cancer Patients Initiating Systemic Cancer Therapy and at High Risk for Venous Thromboembolism
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Catalyst |
Sonstige Studien
[-]
|
Prospektive Beobachtungsstudie bei der Positionierung von Patienten während der Strahlentherapie durch die Anwendung eines optischen Oberflächenscanners (Catalyst™-System)
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CC- 5013-PASS-001 |
Multiples Myelom
[C90.0-]
Blutkrebs (z.B. Leukämie, Lymphome)
[]
|
A non-interventional observational post authorisation safety study of subjects treated with lenalidomide
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CC-486-MDS-006 |
Myelodysplastische Syndrome
[D46.-]
Blutkrebs (z.B. Leukämie, Lymphome)
[]
|
A PHASE 2, INTERNATIONAL, MULTICENTER,
RANDOMIZED, OPEN-LABEL, PARALLEL GROUP
STUDY TO EVALUATE THE EFFICACY AND SAFETY
OF CC-486 (ORAL AZACITIDINE) ALONE AND IN
COMBINATION WITH DURVALUMAB (MEDI4736) IN
SUBJECTS WITH MYELODYSPLASTIC SYNDROMES
WHO FAIL TO ACHIEVE AN OBJECTIVE RESPONSE
TO TREATMENT WITH AZACITIDINE FOR
INJECTION OR DECITABINE
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CC-5013-MDS-010 (PASS) |
Sonstige Studien
[-]
|
A prospective non-interventional post-authorization safety study (PASS), designed as a disease registry of patients with transfusion dependent IPSS low or intermediate-1-risk myelodysplastic syndrome (MDS) and isolated del(5q)
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CC-5013-MM-019 |
Multiples Myelom
[C90.0-]
Blutkrebs (z.B. Leukämie, Lymphome)
[]
|
CC-5013-MM-019 A MULTICENTER, SINGLE-ARM, OPEN-LABEL EXPANDED ACCESS PROGRAMFOR LENALIDOMIDE PLUS DEXAMETHASONE IN PREVIOUSLY TREATED SUBJECTS WITHMULTIPLE MYELOMA
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CC-5013-MM-020 |
Multiples Myelom
[C90.0-]
Blutkrebs (z.B. Leukämie, Lymphome)
[]
|
A Phase III, Randomized,Open-Label, 3-Arm Study to determine theefficacy and safety of lenalidomide (Revlimid) plus low-dose Dexamethasone when given until progressive disease or for safety of lenalidomide (Revlimid) plus low-dose Dexamethasone when given until progressive disease or for 18 four-week cycles versus the combination of Melphalan, Prednisone, and Thalidomide given for 12 six-week cycles in patients with previously untreated multiple myeloma who are either 65 years of age or older or not candidates for stem cell transplantation.
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CC-92480-MM-002 |
Blutkrebs (z.B. Leukämie, Lymphome)
[]
|
A Phase 1/2, Multicenter, Open-label, Study to Determine the Recommended Dose and Regimen, and Evaluate the Safety and Preliminary Efficacy of CC-92480 in Combination with Standard Treatments in Subjects with Relapsed or Refractory Multiple Myeloma (RRMM) and Newly Diagnosed Multiple Myeloma (NDMM)
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CDR0000370860 |
Bösartige Neubildung der Cervix uteri
[C53.-]
Gynäkologische Tumore
[]
|
An international multi center phase III study of chemoradiotherapy versus chemoradiotherapy plus hyperthermia for locally advanced cervical cancer
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