699 |
ja |
Anifrolumab (Saphnelo) |
Anifrolumab Study for Treatment Effectiveness in the Real World
Multi-National, Observational, Post-Launch Effectiveness Study Among
SLE Patients Receiving Anifrolumab in Routine Clinical Practice |
Parexel International GmbH |
AstraZeneca AB |
13.02.2023 |
629 |
ja |
Andexanet alfa; |
Andexanet alfa: Nicht-interventionelle Studie in Stroke Units in Deutschland ASTRO-DE |
Universitätsklinikum Essen, Institut für Medizinische Informatik, Biometrie und Epidemiologie (IMIBE) |
Universitätsklinikum Essen, Institut für Medizinische Informatik, Biometrie und Epidemiologie (IMIBE) |
28.10.2021 |
214 |
ja |
Soliris |
An observational, non-interventional, multi-center, multi-national study of patients with atypical hemolytic-uremic syndrome (aHUS registry) |
Alexion Europe SAS |
|
15.11.2012 |
459 |
nein |
Cablivi 10 mg Pulver und Lösungsmittel zur Herstellung einer Injektionslösung; |
An Observational, Multicenter Study to Evaluate the Safety and Effectiveness of Caplacizumab (ALX0681) in the Treatment of Adults with Acquired Thrombotic Thrombocytopenic Purpura (aTTP) in a Real-life Setting in Germany (OSCAAR) |
AMS Advanced Medical Services GmbH |
Ablynx NV Technologiepark 21 9052 Zwijnaarde, Belgien |
12.10.2018 |
211 |
nein |
Soliris |
An observational, multi-center, multi-national long term follow-up study of atypical hemolytic uremic syndrome (aHUS) patients treated with eculizumab in a prior clinical study |
Alexion Europe SAS |
|
09.10.2012 |
229 |
nein |
Herceptin 150 mg Pulver zur Herstellung eines Infusionslösungskonzentrats |
An Observational Study Of Cardiac Events In Patients With HER2 Positive Early Breast
Cancer Treated With Herceptin (OHERA) |
Roche Pharma AG Grenzach |
F. Hoffmann-La Roche LTD. |
11.03.2013 |
243 |
ja |
Orencia; |
An Observational Registry of Abatacept in Patients with Juvenile Idiopathic Arthritis
Eine Langzeitbeobachtung von Patienten mit JIA welche mit Abatacept (Orencia) behandelt werden. |
Asklepios Klinik St. Augustin |
PRINTO/ Bristol Myers Squibb |
10.10.2013 |
560 |
ja |
Crysvita, Burasumab; |
An international, multicentre, prospective, non-interventional
observational registry for patients with X-linked
hypophosphatemia (XLH) |
IQVIA RDS Slovakia s.r.o. |
Kyowa Kirin International |
06.11.2020 |
249 |
nein |
ORALAIR 100 IR; ORALAIR 100 IR |
ALTO, an international non-interventional registry on the quality of life of patients with grass pollen-induced ALlergic rhinitis treated with ORALAIR |
MAPI Life Sciences (Germany) GmbH |
Stallergenes S.A. |
19.12.2013 |
120 |
ja |
ADVATE 250 I.E./ 500 I.E./ 1000 I.E./ 1500 I.E./ 2000 I.E./ 3000 I.E. Pulver und Lösungsmittel zur Herstellung einer Injektionslösung; ADYNOVI 250 I.E./2 ml Pulver und Lösungsmittel zur Herstellung einer Injektionslösung; ADYNOVI 500 I.E./2 ml Pulver und |
AHEAD: ADVATE/ ADYNOVI Hemophilia A Outcome Database |
AMS Advanced Medical Services GmbH |
Takeda Pharma Vertrieb GmbH & Co. KG Potsdamer Str. 125 10783 Berlin |
27.04.2010 |
219 |
nein |
RoActemra |
ACT-iON, MA27950
A Global Comparative Observational Study in
Rheumatoid Arthritis (RA) Patients who are Treated with
a TNF Inhibitor or Tocilizumab as the First Biologic
Therapy |
Roche Pharma AG |
Roche Pharma AG |
05.12.2012 |
378 |
ja |
|
ACCELERATE: AN INTERNATIONAL, OBSERVATIONAL REGISTRY FOR PATIENTS WITH CASTLEMAN DISEASE |
Parexel International GmbH |
Univ. of Pennsylvania, EUSA Pharma |
11.11.2016 |
499 |
ja |
Takhzyro; |
A three-year, non-interventional, prospective, multicenter study to evaluate the long-term effectiveness of lanadelumab in real-world clinical practice (ENABLE) |
PPD Germany GmbH & Co.KG |
Takeda Development Center Americas, Inc. |
10.09.2019 |
318 |
ja |
Haemate P 250IE, 500IE, 1000 IE; Beriate 250IE, 500IE, 1000 IE, 2000IE; Helixate NexGen 250 I.E./ 500 I.E./ 1000 I.E./ 2000 I.E./ 3000 I.E.; OCTANATE 250 / 500 / 1000 IE; ADVATE 250 I.E./ 500 I.E./ 1000 I.E./ 1500 I.E./ 2000 I.E./ 3000 I.E; ReFacto AF |
A Survey on the Success of Inhibitor Elimination Using Individualized Concentrate Selection and Controlled (High Dose) Immune Tolerance Induction (ITI) |
Hämophilie Zentrum Rhein Main HZRM |
Hämophilie Zentrum Rhein Main HZRM |
10.08.2015 |
570 |
ja |
Guselkumab |
A Substudy of CNTO1959PSA4001 (PsABIOnd) to Assess the Qualitative Impact of Guselkumab (TREMFYA®) and IL-17 Inhibitor Therapies in Patients with Psoriatic Arthritis via a Digital and Wearable Patient Application |
Parexel International GmbH. |
Janssen-Cilag International NV |
24.02.2021 |
330 |
ja |
NOVOCART Inject |
A retrospective, non-interventional study on the reconstruction of localized, full-thickness cartilage defects of the knee joint using an in situ polymerizable and chondrocyte-populated biomaterial (NOVOCART INJECT)
"RENOVO" |
TETEC AG |
|
05.11.2015 |
350 |
ja |
Soliris |
A RETROSPECTIVE DATA COLLECTION OF THE CLINICAL CHARACTERISTICS OF
PATIENTS WITH PAROXYSMAL NOCTURNAL HEMOGLOBINURIA |
Pharmaceutical Research Associates GmbH |
Amgen, Inc., Global Biosimilars |
01.04.2016 |
331 |
ja |
|
A Retrospective Cohort Study of PD-L1 in Recurrent and Metastatic Squamous Cell Carcinoma of Head and Neck |
QuintilesIMS |
AstraZeneca |
06.11.2015 |
745 |
ja |
Blenrep; THALOMID; VELCADE; KYPROLIS; NINLARO; |
A real-world study to assess treatment patterns and outcomes of patients with relapsed or refractory multiple myeloma who have received at least one prior line of therapy in the United Kingdom, Italy, and Germany |
GlaxoSmithKline, LLC |
Analysis Group, Inc. |
14.11.2023 |
727 |
ja |
Skyrizi 360 mg Injektionslösung in einer; Skyrizi 600 mg Konzentrat zur Herstellung einer Infusionslösung |
A Prospective, Post-marketing, non-interventional study of RISankizumab evaluating real-world clinical Effectiveness in Crohn’s disease (APPRISE) |
Abbvie Deutschland GmbH & Co KG |
Abbvie Deutschland GmbH & Co KG |
10.08.2023 |
505 |
ja |
DARZALEX; VELCADE; |
A Prospective, Multinational Study of Real-Life Current Standards of Care in Patients with Relapsed and/or Refractory Multiple Myeloma Who Received at Least 3 Prior Lines of Therapy Including PI, IMiD, and CD38 Monoclonal Antibody Treatment |
Janssen-Cilag GmbH |
|
08.11.2019 |
649 |
ja |
DARZALEX; VELCADE; |
A Prospective, Multinational Study of Real-Life Current Standards of Care in Patients with Relapsed and/or Refractory Multiple Myeloma |
Janssen-Cilag GmbH |
Janssen-Cilag GmbH |
17.02.2022 |
312 |
ja |
Lemtrada; |
A prospective, multicenter, observational, post-authorization safety study (PASS) to evaluate
the long term safety profile of LEMTRAD® (alemtuzumab) treatment in patients with
relapsing forms of multiple sclerosis (RMS) (OBS13434) |
Sanofi-Aventis Deutschland GmbH |
|
21.07.2015 |
747 |
ja |
|
A Prospective Study to Evaluate Disease Characteristics in Hemophilia B Participants Receiving Prophylaxis with Standard of Care FIX Replacement Therapy |
ICON Clinical Research Germany GmbH |
Regeneron Pharmaceuticals, Inc |
24.11.2023 |
233 |
nein |
Remicade/Simponi |
A Prospective Observational Study to Evaluate the Relationship between Disease State and Change in Quality of Life in Ankylosing Spondylitis Patients treated with Remicade (infliximab) or Simponi (golimumab) |
Quitiles - Outcome Europe |
Merck Sharp & Dohme Corp. |
28.05.2013 |