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| ID | Type | Description | Link |
|---|---|---|---|
| 2021-002300-12 | EudraCT Number | ||
| 01EN2001 | Other Grant/Funding Number | German Federal Ministry of Education and Research | |
| DRKS00025884 | Registry Identifier | German Clinical Trials Register |
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| Name | Class |
|---|---|
| Ruhr University of Bochum | OTHER |
| University Medicine Greifswald | OTHER |
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The study will assess the safety of low doses of epirubicin in sepsis patients. Therefore the study will look for side effects in patients treated with low dose epirubicin compared to control patients.
In animals, low dose epirubicin has been shown to induce tolerance to infection and increase survival in septic mice.
The study will also look for positive effects on organ function in humans. The investigators hypothesize that low-dose epirubicin can be used therapeutically to improve the disease course and lessen mortality of patients with sepsis. In a first step, the investigators aim at proving that low-dose epirubicin can safely be administered to sepsis patients and will perform a dose-escalation multi-center trial.
There are two ways for organism to deal with infection. Resistance, which means elimination of infectious microorganisms by the immune system, is widely recognized. It can be supported by antibiotic medication and surgical or interventional drainage of an infectious focus. The other response is tolerance, which means limiting organ damage without fighting the infection itself. Its importance has become more clearly recently, but so far there are no therapeutic interventions to support this mechanism.
Epirubicin is a chemotherapeutic substance used to treat cancer. In animal experiments, it has been shown that doses much lower than the ones used in oncology, can induce tolerance in infected animals. Animals treated with epirubicin survive an infectious dose that kills animals not treated with epirubicin. Before this approach can be studied in a large group of sepsis patients, it is necessary that epirubicin in low doses can be safely used in this population.
Therefore in this study, septic patients will be treated with low doses of epirubicin and systematically assessed for serious side effects. Some patients will be treated with placebo for comparison. The trial will be conducted as a dose escalation study with three groups. This means that the first group of patients will receive only a quarter of the dose shown to be effective in animal experiments. Only if no serious side effects are observed will the dose be increased in the second group and again in the third group.
In addition, the study will look for signs of beneficial effects on organ function in human patients with sepsis, pharmacokinetics of epirubicin in sepsis patients and changes in the inflammatory response.
The investigators hypothesize that low-dose epirubicin can be used therapeutically to improve the disease course and lessen mortality of patients with sepsis. In a first step, the investigators aim at proving that low-dose epirubicin can safely be administered to sepsis patients and will perform a phase IIa dose-escalation multi-center trial.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Placebo | Placebo Comparator | Administration of NaCl i.v. as placebo once. |
|
| Epirubicin Phase I | Experimental | Administration of epirubicin i.v. 3.75 mg/m2 once. |
|
| Epirubicin Phase II | Experimental | Administration of epirubicin i.v. 7.5 mg/m2 once. |
|
| Epirubicin Phase III | Experimental | Administration of epirubicin i.v. 15 mg/m2 once. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Epirubicin | Drug | Epirubicin is given once over 15 Minutes via a central line |
|
| Measure | Description | Time Frame |
|---|---|---|
| Number of participants with myelotoxicity | Neutropenia or thrombocytopenia of grade 3 or 4 (neutrophiles <1,000μL or platelets <50,000/μL) at two consecutive study visits up to day 14 accompanied by neutropenia or thrombocytopenia of grade 2, 3 or 4 (neutrophiles <1,500μL or platelets <75,000/μL) at both study visits and accompanied by an IPF (immature platelet fraction) below 2.5% at one or two of the consecutive study visits. | Up to 14 days after administration of study drug |
| Measure | Description | Time Frame |
|---|---|---|
| Survival at day 14, 28 and 90 | Survival | 14, 28 and 90 days |
| SOFA score | SOFA (sequential organ failure assessment) on days of assessment, mean total SOFA and SOFA changes over time |
| Measure | Description | Time Frame |
|---|---|---|
| Epirubicin plasma concentrations | Epirubicin concentrations in the plasma will be measured using mass-spectrometry | At 15minutes and at 1, 2, 3, 6, 12, and 24 hours after administration of study drug |
| DNA damage |
Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Sebastian Weis, M.D. | Contact | +49 (0) 3641-932 | 3100 | Sebastian.Weis@med.uni-jena.de |
| Daniel O Thomas-Rüddel, M.D. | Contact | +49 (0) 3641-932 | 3267 | Daniel.Thomas@med.uni-jena.de |
| Name | Affiliation | Role |
|---|---|---|
| Sebastian Weis, M.D. | Jena University Hospital | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Jena University Hospital | Recruiting | Jena | Thuringia | 07747 | Germany |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 24184056 | Background | Figueiredo N, Chora A, Raquel H, Pejanovic N, Pereira P, Hartleben B, Neves-Costa A, Moita C, Pedroso D, Pinto A, Marques S, Faridi H, Costa P, Gozzelino R, Zhao JL, Soares MP, Gama-Carvalho M, Martinez J, Zhang Q, Doring G, Grompe M, Simas JP, Huber TB, Baltimore D, Gupta V, Green DR, Ferreira JA, Moita LF. Anthracyclines induce DNA damage response-mediated protection against severe sepsis. Immunity. 2013 Nov 14;39(5):874-84. doi: 10.1016/j.immuni.2013.08.039. Epub 2013 Oct 31. | |
| 38653508 |
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| ID | Term |
|---|---|
| D018805 | Sepsis |
| ID | Term |
|---|---|
| D007239 | Infections |
| D018746 | Systemic Inflammatory Response Syndrome |
| D007249 | Inflammation |
| D010335 | Pathologic Processes |
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| ID | Term |
|---|---|
| D015251 | Epirubicin |
| ID | Term |
|---|---|
| D004317 | Doxorubicin |
| D003630 | Daunorubicin |
| D018943 | Anthracyclines |
| D009279 | Naphthacenes |
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Sequential dose escalation with three dosing groups and placebo.
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Study medication is provided in colored infusion bags with additional covers
| Placebo | Drug | NaCl is given once over 15 Minutes via a central line |
|
| Up to 14 days after administration of study drug |
| Cardiotoxicity | Ejection fraction measured via TTE (trans-thoracic echocardiography) | 7 days after administration of study drug |
| "Success" rate | Decrease of procalcitonin (PCT) serum concentration by 80% or more of its intra-individual peak value or to 0.5 μg/L or lower within 72 hours after randomization | 3 days after administration of study drug |
| Adverse events | Overall rate of adverse and severe adverse events. The the frequency of other typical side effects (diarrhea, mucositis, alopecia, nausea and vomiting). | Up to 90 days after administration of study drug |
| Quality of life assesed by the SF-36 questionaire | The short Form 36 Health Questionnaire (SF-36) contains 36 questions on quality of life. From the answers a Physical Component Summary (PCS) and a Mental Component Summary (MCS) are calculated, both ranging approximately from 0 (severe disability) up to 80 (absence of disability). | At follow up 90 days after administration of study drug |
| Fluid balance and urine output | Assessment of fluid balance and urine output | Up to 14 days after administration of study drug |
| Need for renal replacement therapy | Use of renal replacement therapy for chronic or acute kidney failure | Up to 14 days after administration of study drug |
| Oxygenation index (paO2/FiO2) | The ratio of arterial oxygen partial pressure and the fraction of inhaled oxygen will be calculated. For patients receiving conventional low flow oxygen FiO2 will be estimated based on a predefined table. | Up to 14 days after administration of study drug |
| Need for respiratory support | The highest level of respiratory support will be documented. | Up to 14 days after administration of study drug |
| Need for catecholamines and inotropes | For all catecholamines and inotropes the highest daily rate administerd for at least one hour will be documented. | Up to 14 days after administration of study drug |
DNA damage in peripheral mononuclear blood cells (PBMC) will be assessed. Further assessment of molecular parameters from the PBMCs reflecting epirubicin effects on the DNA or damage control pathways will be performed subsequently
| Up to 7 days after administration of study drug |
| Cytokines | Plasma cytokines will be determined in all patients using Luminex xMAP or alike multiplex technology | Up to 14 days after administration of study drug |
| Organ damage markers | Non-conventional sensitive organ damage markers (e.g. NGAL) will be measured | Up to 14 days after administration of study drug |
| Anti-PF4 anti-bodies | Determination of anti-PF4 (platelet factor 4) anti-bodies | Up to 14 days after administration of study drug |
| Mitochondrial function | Molecular parameters for mitochondrial function will be assessed from isolated PBMCs | Up to 7 days after administration of study drug |
| University Hospital Knappschafstkrankenhaus Bochum | Not yet recruiting | Bochum | 44892 | Germany |
|
| University Medicine Greifswald | Not yet recruiting | Greifswald | 17489 | Germany |
|
| Universitätsklinikum Hamburg Eppendorf | Not yet recruiting | Hamburg | 20251 | Germany |
|
| Universitätsklinikum Würzburg | Not yet recruiting | Würzburg | 97080 | Germany |
|
| Derived |
| Thomas-Ruddel D, Bauer M, Moita LF, Helbig C, Schlattmann P, Ehler J, Rahmel T, Meybohm P, Grundling M, Schenk H, Kocher T, Brunkhorst FM, Graler M, Heger AJ, Weis S; EPOS-1 study group; SepNetCriticalCare TrialsGroup. Epirubicin for the Treatment of Sepsis and Septic Shock (EPOS-1): study protocol for a randomised, placebo-controlled phase IIa dose-escalation trial. BMJ Open. 2024 Apr 22;14(4):e075158. doi: 10.1136/bmjopen-2023-075158. |
| D013568 |
| Pathological Conditions, Signs and Symptoms |
| D011084 |
| Polycyclic Aromatic Hydrocarbons |
| D006841 | Hydrocarbons, Aromatic |
| D006844 | Hydrocarbons, Cyclic |
| D006838 | Hydrocarbons |
| D009930 | Organic Chemicals |
| D011083 | Polycyclic Compounds |
| D000617 | Aminoglycosides |
| D006027 | Glycosides |
| D002241 | Carbohydrates |