Search Results - "Fudio, Salvador"
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Integrated exposure–response analysis of efficacy and safety of lurbinectedin to support the dose regimen in small-cell lung cancer
Published in Cancer chemotherapy and pharmacology (01-05-2022)“…Purpose These exposure–response (E–R) analyses integrated lurbinectedin effects on key efficacy and safety variables in relapsed SCLC to determine the adequacy…”
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Quantitative determination of lurbinectedin, its unbound fraction and its metabolites in human plasma utilizing ultra-performance LC-MS/MS
Published in PloS one (30-03-2023)“…Ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) methods to quantify total lurbinectedin, its plasma protein binding to derive the…”
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A phase I trial of lurbinectedin in combination with cisplatin in patients with advanced solid tumors
Published in Investigational new drugs (01-02-2022)“…Summary Background In vitro / in vivo data showed synergism of cisplatin and lurbinectedin in ovarian cancer cells and grafts. This phase I trial investigated…”
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Pharmacokinetics and Safety of Lurbinectedin Administrated with Itraconazole in Cancer Patients: A Drug-Drug Interaction Study
Published in Marine drugs (01-04-2024)“…This open-label, two-part, phase Ib drug-drug interaction study investigated whether the pharmacokinetic (PK) and safety profiles of lurbinectedin (LRB), a…”
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A model-based head-to-head comparison of single-agent lurbinectedin in the pivotal ATLANTIS Study
Published in Frontiers in oncology (15-06-2023)“…Lurbinectedin is a selective inhibitor of oncogenic transcription U.S. Food and Drug Administration (FDA)-approved for patients with relapsed small cell lung…”
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Effect of lurbinectedin on the QTc interval in patients with advanced solid tumors: an exposure–response analysis
Published in Cancer chemotherapy and pharmacology (01-01-2021)“…Purpose This study assessed the effect of lurbinectedin, a highly selective inhibitor of oncogenic transcription, on the change from baseline in Fridericia’s…”
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Impact of a Moderate CYP3A4 Inducer (Bosentan) on Lurbinectedin Pharmacokinetics and Safety in Patients with Advanced Solid Tumors: An Open-Label, Two-Way, Crossover, Phase Ib Drug-Drug Interaction Study
Published in Pharmaceuticals (Basel, Switzerland) (30-01-2024)“…This open-label, two-way, crossover, phase Ib drug-drug interaction study investigated whether the pharmacokinetics (PKs) and safety profile of lurbinectedin…”
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Phase I study of plitidepsin in combination with bortezomib and dexamethasone in patients with relapsed/refractory multiple myeloma
Published in Cancer medicine (Malden, MA) (01-02-2023)“…Previous studies showed antitumor activity for plitidepsin plus dexamethasone (DXM) in relapsed/refractory multiple myeloma (r/r MM), and in vitro synergism…”
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Evaluation of the influence of sex and CYP2C19 and CYP2D6 polymorphisms in the disposition of citalopram
Published in European journal of pharmacology (25-01-2010)“…We investigate the impact of sex and genotype on citalopram disposition in 35 healthy volunteers who received an oral dose of 20 mg citalopram within a…”
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Population-Pharmacokinetic and Covariate Analysis of Lurbinectedin (PM01183), a New RNA Polymerase II Inhibitor, in Pooled Phase I/II Trials in Patients with Cancer
Published in Clinical pharmacokinetics (01-03-2019)“…Background and Objectives Lurbinectedin is an inhibitor of RNA polymerase II currently under clinical development for intravenous administration as a single…”
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Population Pharmacokinetic‐Pharmacodynamic Modeling and Covariate Analyses of Neutropenia and Thrombocytopenia in Patients With Solid Tumors Treated With Lurbinectedin
Published in Journal of clinical pharmacology (01-09-2021)“…Lurbinectedin is a selective inhibitor of oncogenic transcription. Reversible myelosuppression is its most relevant toxicity. Pharmacokinetic‐pharmacodynamic…”
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Anti-cancer drug combinations approved by US FDA from 2011 to 2021: main design features of clinical trials and role of pharmacokinetics
Published in Cancer chemotherapy and pharmacology (01-10-2022)“…During the last decade, the treatment for many cancer indications has evolved due to intensive clinical research into anti-tumor agents’ combination. In most…”
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A phase I safety and efficacy clinical trial of plocabulin and gemcitabine in patients with advanced solid tumors
Published in Investigational new drugs (03-08-2024)“…Plocabulin (Plo) induces depolymerization of tubulin fibers with disorganization and fragmentation of the microtubule network leading to mitosis. Plo combined…”
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First-in-human phase I study of the microtubule inhibitor plocabulin in patients with advanced solid tumors
Published in Investigational new drugs (01-08-2019)“…Summary Background Plocabulin (PM060184) is a novel marine-derived microtubule inhibitor that acts as an antitumor agent. This first-in-human study evaluated…”
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First-in-human study of PM14 in patients with advanced solid tumors
Published in Journal of clinical oncology (20-05-2021)“…Abstract only 3078 Background: PM14 is a new chemical entity that forms DNA adducts which specifically inhibit RNA synthesis and block active transcription of…”
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Quantitative determination of lurbinectedin, its unbound fraction and its metabolites in human plasma utilizing ultra-performance LC–MS/MS
Published in PloS one (01-01-2023)“…Aims Ultra-performance liquid chromatography–tandem mass spectrometry (UPLC–MS/MS) methods to quantify total lurbinectedin, its plasma protein binding to…”
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17
Preclinical and randomized phase I studies of plitidepsin in adults hospitalized with COVID-19
Published in Life science alliance (01-04-2022)“…Plitidepsin, a marine-derived cyclic-peptide, inhibits SARS-CoV-2 replication at nanomolar concentrations by targeting the host protein eukaryotic translation…”
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Phase I dose-escalation study of plitidepsin in combination with sorafenib or gemcitabine in patients with refractory solid tumors or lymphomas
Published in Anti-cancer drugs (01-03-2017)“…This phase I trial evaluated the combination of the marine-derived cyclodepsipeptide plitidepsin (trade name Aplidin) with sorafenib or gemcitabine in advanced…”
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Valproate-meropenem co-administration, an example of information shortcomings in relevant drug interactions
Published in Medicina clínica (30-05-2009)Get more information
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Overuse of PPIs in patients at admission, during treatment, and at discharge in a tertiary Spanish hospital
Published in Current clinical pharmacology (01-11-2010)“…The first generic PPI was introduced in Spain in 2001, and since then their prescriptions have increased steadily by about 200%. To evaluate the frequency of…”
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