- Rekrutierung läuft
ADOREG - Bundesweites prospektives Register zur Versorgungsforschung in der dermatologischen Onkologie
- Rekrutierung läuft
Multicenter Trial of Talimogene laherparepvec in Combination with Pembrolizumab for Treatment of Unresectable Stage IIIB to IV M1c Melanoma (MASTERKEY-265)
IndikationenMolekulare Marker - Rekrutierung läuftEncorafenib Plus Binimetinib in Patients With Locally Advanced, Unresectable or Metastatic BRAFV600-mutated Melanoma: a Multi-centric, Multinational, Prospective, Longitudinal, Non-interventional Study in Germany, Austria and SwitzerlandIndikationenMolekulare Marker
- Rekrutierung läuft
A Phase 3, Randomized, Open-label Study of NKTR-214 Combined with Nivolumab Versus Nivolumab in Participants with Previously Untreated Unresectable or Metastatic Melanoma
Indikationen - Rekrutierung läuftA Phase 1/2a Dose Escalation and Cohort Expansion Study of the Safety, Tolerability, and Efficacy of Anti-LAG-3 Monoclonal Antibody (BMS-986016) Administered Alone and in Combination with Anti-PD-1 Monoclonal Antibody (Nivolumab, BMS-936558) in Advanced Solid TumorsIndikationenMolekulare Marker
- Rekrutierung läuft
A Randomized, Double-Blind Phase 2/3 Study of Relatlimab Combined with Nivolumab versus Nivolumab in Participants with Previously Untreated Metastatic or Unresectable Melanoma
IndikationenMolekulare Marker - Rekrutierung läuft
A PHASE I, FIRST IN HUMAN, TWO PART, OPEN-LABEL CLINICAL TRIAL OF INTRAVENOUS ADMINISTRATION OF CTL-002 GIVEN AS MONOTHERAPY AND/OR IN COMBINATION WITH AN ANTI-PD-1 CHECKPOINT-INHIBITOR IN SUBJECTS WITH ADVANCED STAGE, RELAPSED/REFRACTORY SOLID TUMORS
Molekulare Marker - Rekrutierung läuftDirekte Detektion von Immunmolekülen im Malignen MelanomIndikationenMolekulare Marker
- Rekrutierung läuftCombination of Targeted Therapy (Encorafenib and Binimetinib) Followed by Combination of Immunotherapy (Ipilimumab and Nivolumab) vs Immediate Combination of Immunotherapy in Patients With Unresectable or Metastatic Melanoma With BRAF V600 Mutation : an EORTC Randomized Phase II Study (EBIN)Indikationen
- Rekrutierung läuftA first-in-human, two-part, open-label, clinical study to assess the safety, tolerability and activity of intravenous doses of ICT01 as monotherapy and in combination with an immune checkpoint inhibitor, in patients with advanced-stage, relapsed/refractory cancer (EVICTION Study)Indikationen
- Brustkrebs (Mammakarzinom)
- Bösartige Erkrankungen des oberen Verdauungstraktes (Oesophagus, Magen, gastrooesophagealer Übergang)
- Karzinom des gastrooesophagealen Übergangs
- Magenkarzinom
- Weitere Tumoren des Verdauungstraktes (z.B. Gastrointestinale Stromatumoren, GIST)
- Lungentumoren
- Nicht-kleinzelliges Bronchialkarzinom (NSCLC)
- Kopf/Hals Tumoren
- Kopf-Hals-Malignome
- Hauttumoren
- Malignes Melanom
- Lymphome inkl. Morbus Hodgkin, Multiples Myelom und Chronisch Lymphatischer Leukämie (CLL)
- Non-Hodgkin Lymphome (inkl. Chron. Lymphat. Leukämie, CLL)
- Leukämien
- Akute lymphatische Leukämie und Burkitt-Lymphom (ALL)
- Akute myeloische Leukämie (AML)