Clinical Research Directory

Inclusion Criteria: * Age equal to or above 18 years * Patients of either gender * Written informed consent provided by the patient. For patients without decision-making capacity, informed consent must be obtained from a legally designated representative following the national legislation. * Negative (blood or urinary) pregnancy test for female patients of reproductive age * For female patients of reproductive age, willingness to use highly effective contraception during and seven days after the administration of the IMP. * Presence of Community-acquired pneumonia (CAP) * Presence of sepsis as defined by the Sepsis-3 classification criteria (at least 2 points increase of the total SOFA-1 score from the baseline score of the specific patient). The SOFA score which will be used for the definition of sepsis has recently been renamed SOFA-1. * Absolute lymphocyte count (ALC) less than 1000/mm³. Exclusion Criteria: * Age below 18 years * Denial of written informed consent * Pregnancy (confirmed by blood or urinary pregnancy test) or lactation for female patients * Unwillingness to receive contraception during and seven days after the administration of the IMPstudy drug (for Female patients) * Known HIV infection with known CD4 cell count \<200/mm³ * Solid organ or bone marrow transplantation * Corticosteroid oral or intravenous intake greater than 0.4mg/kg of equivalent prednisone daily over the last 15 days or other immunosuppressive therapy. However, corticosteroids received as adjunctive treatment for the current septic/infectious episode are allowed * Intake of a biological agent in the last month * Known active neoplasms or other conditions unrelated to sepsis that compromise short-term survival less than 6 months * Neutropenia \< 500/mm³ * Intake of any macrolide for the current episode of CAP under study * QTc interval at rest in the ECG ≥500 msec or history of known long QT syndrome * Medical history of allergy to macrolides * Concomitant use of medicinal products contraindicated with clarithromycin, including CYP3A substrates associated with QT prolongation (e.g., astemizole, cisapride, domperidone, pimozide, terfenadine, ivabradine), ergot alkaloids (e.g., ergotamine, dihydroergotamine), oral midazolam, HMG-CoA reductase inhibitors primarily metabolised by CYP3A4 (e.g., lovastatin, simvastatin), colchicine, ticagrelor, and ranolazine. This criterion applies to all medicinal products within these classes, not only the specific examples listed, in accordance with the SmPC for clarithromycin. Patients may be enrolled provided that such medications are discontinued prior to or at the time of trial participation. Given their short half-life, no wash-out period is required * Medical history of torsades de pointes arrhythmia * Severe hypokalemia or hypomagnesemia; patients may be enrolled once these electrolyte abnormalities are corrected. * Any contradictions for macrolide uptake * Previous participation in the CLASSIFY study * Participation in any other interventional trial within the last 30 days * Severe hepatic failure in combination with renal impairment