Dr. Martin Fehr
Medizinische Onkologie und Hämatologie · Dept. I
CAR T- Cell EBMT Registry data processing framework
Jul 30, 2021
Clinical Studies - Jul 30, 2021 - Dec 31, 2026
Ongoing
Project leader: Fehr Martin
Members: Breuss Kim, Frehner Jan
A Study to Evaluate Imetelstat (GRN163L) in Transfu-sion-Dependent Subjects with IPSS Low or Intermedi-ate-1 Risk Myelodysplastic Syndrome (MDS) that is Re-lapsed/Refractory to Erythropoiesis-Stimulating Agent (ESA) Treatment
Mar 15, 2021A Study to Evaluate Imetelstat (GRN163L) in Transfu-sion-Dependent Subjects with IPSS Low or Intermedi-ate-1 Risk Myelodysplastic Syndrome (MDS) that is Re-lapsed/Refractory to Erythropoiesis-Stimulating Agent (ESA) Treatment
Clinical Studies - Mar 15, 2021 - Apr 7, 2030
Scheduled
Project leader: Silzle Tobias
Members: Driessen Christoph, Fehr Martin, Hitz Felicitas, Lehmann Thomas
EMCL-Registry of the European Mantle Cell Lymphoma study group
Dec 20, 2019Klinisches Register des „Europäischen Mantelzelllymphom Netzwerk (EMCL)“. Erfassung von Patienten mit neu diag-nostiziertem oder rezidiviertem Mantelzelllymphom
Clinical Studies - Dec 20, 2019 - Dec 20, 2025
Scheduled
Project leader: Fehr Martin
EMCL-Registry of the European Mantle Cell Lymphoma study group
Dec 20, 2019
Clinical Studies - Dec 20, 2019 - Dec 31, 2030
Ongoing
Project leader: Fehr Martin
Members: Steiner Marianne, Frehner Jan
SAKK 30/15; HOVON 135: A randomized phase II multicenter study to assess the to erability and efficacy of the addition of ibrutinib to 10-day decitabine in UNFIT (i.e. HCT-CI ≥ 3) AML and high risk myelodysplasia (MDS) (IPSS-R > 4.5) patients aged ≥ 66 years. A study in the frame of the masterprotocol of parallel randomized phase II studies in UNFITolder AML/high-risk MDS patients
Oct 27, 2016This is a prospective, open label, multicenter study that is conducted in the frame of a masterprotocol with multiple parallel randomized phase II arms. The scheme of this design consists of one arm with the standard treatment for AML (the 10-day dec...
Clinical Studies - Oct 27, 2016 - Jul 31, 2018
Automatically Closed
Project leader: Fehr Martin
Merck EORTC 1325 / MK-3475-054 - Adjuvant immunotherapy with anti-PD-1 monoclonal anti-body Pembrolizumab (MK-3475) versus placebo after complete resection of high-risk Stage III melanoma: A ran-domized, double- blind Phase 3 trial of the EORTC Mela-noma Group
Mar 1, 2016This is an international, double-blinded, placebo-controlled randomized phase III trial. Enrollment will be a multi-step process. Randomization (placebo vs. pembrolizumab) will be performed centrally and will be stratified for the following factors:...
Clinical Studies - Mar 1, 2016 - Mar 1, 2020
Automatically Closed
Project leader: Fehr Martin
Rituximab with or without Ibrutinib for untreated patients with advanced follicular lymphoma in need of therapy. A randomized, double-blinded, SAKK and NLG collaborative Phase II trial
Oct 15, 2015Der Behandlungsansatz beim FL sah bislang entweder ein zunächst abwartendes Beobachten beim asymptomati-schen Patienten oder aber monotherapeutische Behand-lungen vor, mit dem Ziel, möglichst lange eine gute Le-bensqualität zu erhalten. Für die asymp...
Clinical Studies - Oct 15, 2015 - Dec 31, 2029
Ongoing
Project leader: Hitz Felicitas
Members: Silzle Tobias, Fehr Martin, Fischer Stefanie
Combination of ibrutinib and bortezomib followed by ibrutinib maintenance to treat patients with relapsed and refractory mantle cell lymphoma; a multicenter Phase I/II trial
Sep 9, 2015Das Mantelzelllymphom zeichnet sich durch eine für B-Zell Lymphome vergleichsweise schlechte Prognose aus. Dies erklärt sich durch häufige Rückfälle und dem meist ausgedehnten Krankheitsstadium und höherem Alter (median 60-65 Jahre) bei Diagnosestell...
Clinical Studies - Sep 9, 2015 - Mar 31, 2021
Automatically Closed
Project leader: Driessen Christoph
Members: Hitz Felicitas, Fehr Martin, Hess Urs, Hess Dagmar, Silzle Tobias
HOVON 103 / SAKK 30/10 protocol Tosedostat
Mar 19, 2015A randomized phase II multicenter study with a safety run-in to assess the tolerability and efficacy of the addition of oral tosedostat to standard induction therapy in AML and high risk myelodysplasia (MDS) (IPSS-R risk score > 4.5) in patients aged...
Clinical Studies - Mar 19, 2015 - Mar 19, 2015
Automatically Closed
Project leader: Hess Urs
Members: Hitz Felicitas, Baumann Michael, Driessen Christoph, Fehr Martin, Silzle Tobias