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    A Phase 2, Open-Label, Monotherapy, Multicenter Study to Evaluate the Efficacy and Safety of INCB054828 in Subjects With Myeloid/Lymphoid Neoplasms With FGFR1 Rearrangement

    * All potential subjects must have documentation of an 8p11 translocation known to activate FGFR1 through the site's own cytogenetics laboratory. * Once documentation has been provided, the subject will then undergo screening to meet the rest of the inclusion/exclusion criteria. * Once a subject has completed screening and has enrolled into the study, treatment will start on Cycle 1 Day 1. * Subjects will undergo regular safety assessments during treatment as well as regular efficacy assessments. * Subjects will be allowed to continue administration in 21-day cycles until loss of benefit from therapy or unacceptable toxicity is reported.

    Phase

    2

    Span

    Sponsor

    Mannheim, Baden-Wuerttemberg

    Recruiting

  • Study Investigating Patient-Reported Outcomes in Lower-risk MDS Patients

    Phase

    N/A

    Span

    129 weeks

    Sponsor

    University of Leipzig

    Mannheim

    Recruiting

  • Treatment of Non-resectable Bile Duct Cancer with Radiofrequency Ablation or Photodynamic Therapy

    Klatskin tumours are a form of bile duct cancer. They are generally not diagnosed until quite late and a curative operation is rarely a possibility. Their anatomic location usually results in bile duct obstruction and the aim of therapy is thus to keep the ducts open. This is accomplished through endoscopic retrograde cholangiopancreatography (ERCP) by implanting stents. Stent therapy combined with photodynamic therapy (PDT) extends life expectancy. PDT requires an injection of photosensitizer that is absorbed primarily by the cancer cells. Light of a particular wavelength is then applied with ERCP to kill the cancer cells. Drawbacks include not only high costs and poor availability, but foremost that patients have to avoid direct sunlight for a period of weeks. Radio frequency ablation (RFA) together with stent implantation constitutes an alternative by which the cancer cells are killed through heat applied during ERCP. The RFA technology is more widely available and easier to deploy. However, it has not been studied extensively and no randomized trials exist comparing the two methods. This trial will compare survival in patients with Klatskin tumours depending on whether they receive PDT or RFA. Moreover, data will be collected on side-effects and quality of life.

    Phase

    4

    Span

    273 weeks

    Sponsor

    University of Leipzig

    Mannheim

    Recruiting

  • Cardiogenic Shock Registry Mannheim

    All consecutive patients with a confirmed cardiogenic shock presenting at the internal intensive care Unit (ICU) at the University of Mannheim are included in the register and followed up during ICU stay and after that. Data of patients' admission status, cause of cardiogenic shock, baseline parameters and comorbidities are collected. Extensive information about echocardiography, electrocardiography and imaging procedures are included in the register. Laboratory values, microbiological investigations, organ dysfunction and organ replacement therapies, medication, adverse events, and complications were recorded for several days during the ICU stay (days 1, 2, 3, 5, 7, and 8). Standard scores for critically ill patients were calculated for the day of admission at the ICU if available, and several time points during the ICU stay. The register includes information about the mortality during ICU stay, 30-day mortality, 6-month mortality and 1-year mortality.

    Phase

    N/A

    Span

    235 weeks

    Sponsor

    Universitätsmedizin Mannheim

    Mannheim

    Recruiting

  • Heart Failure With Mildly Reduced Ejection Fraction Registry

    Phase

    N/A

    Span

    418 weeks

    Sponsor

    Universitätsmedizin Mannheim

    Mannheim

    Recruiting

  • Suprasorb® CNPendo Used for Negative Pressure Therapy in the Oesophagus and Rectum to Support Defect and Wound Healing

    Phase

    N/A

    Span

    174 weeks

    Sponsor

    Lohmann & Rauscher

    Mannheim

    Recruiting

  • A Study to Investigate the Efficacy and Safety of Efgartigimod PH20 SC in Adult Participants With Active Idiopathic Inflammatory Myopathy.

    Phase

    2/3

    Span

    225 weeks

    Sponsor

    argenx

    Mannheim

    Recruiting

  • A Study of Donanemab (LY3002813) in Participants With Early Symptomatic Alzheimer's Disease (TRAILBLAZER-ALZ 5)

    TRAILBLAZER-ALZ 5 is a Phase 3, double-blind, placebo-controlled study to evaluate the safety and efficacy of donanemab in participants with early symptomatic AD (prodromal AD and mild dementia due to AD) with the presence of brain tau pathology.

    Phase

    3

    Span

    238 weeks

    Sponsor

    Eli Lilly and Company

    Mannheim, Baden-Württemberg

    Recruiting

  • Safety and Efficacy of Intra-arterial Tenecteplase for Noncomplete Reperfusion of Intracranial Occlusions

    Phase

    3

    Span

    198 weeks

    Sponsor

    Insel Gruppe AG, University Hospital Bern

    Mannheim

    Recruiting

  • Selinexor in Maintenance Therapy After Systemic Therapy for Participants With p53 Wild-Type, Advanced or Recurrent Endometrial Carcinoma

    Phase

    3

    Span

    250 weeks

    Sponsor

    Karyopharm Therapeutics Inc

    Mannheim

    Recruiting

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