Ana Del Campo García

ORCID: 0000-0003-2709-5583
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About
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Research Areas
  • Biosimilars and Bioanalytical Methods
  • Colorectal Cancer Treatments and Studies
  • Pharmacogenetics and Drug Metabolism
  • Amyloidosis: Diagnosis, Treatment, Outcomes
  • Pancreatitis Pathology and Treatment
  • Pharmaceutical Economics and Policy
  • Sarcoma Diagnosis and Treatment
  • Organ Donation and Transplantation
  • Multiple Myeloma Research and Treatments
  • CAR-T cell therapy research
  • Inflammatory mediators and NSAID effects
  • Testicular diseases and treatments
  • Drug Transport and Resistance Mechanisms
  • Chronic Lymphocytic Leukemia Research
  • Neutropenia and Cancer Infections
  • Computational Drug Discovery Methods
  • Renal and Vascular Pathologies
  • Gastrointestinal Bleeding Diagnosis and Treatment
  • Lung Cancer Treatments and Mutations
  • Chronic Kidney Disease and Diabetes
  • Dialysis and Renal Disease Management
  • IgG4-Related and Inflammatory Diseases
  • Esophageal and GI Pathology
  • Pharmaceutical studies and practices
  • Synthesis and Biological Evaluation

The University of Texas Health Science Center at San Antonio
2024

Hospital Virgen de la Salud
2019-2022

Hospital General de México
2005-2018

Light Prescriptions Innovators (Spain)
2018

Hospital General de Elda
2003-2005

The main objective was to quantify any potential differences in pharmacokinetic (PK) parameters (AUC and Cmax) between RTXM83, a proposed rituximab biosimilar, its reference product, using population PK model approach.Rituximab PD data were obtained from randomized, double-blind, phase III clinical study (RTXM83-AC-01-11) patients with diffuse large B-cell lymphoma (DLBCL) that received 375 mg/m2 intravenous RTXM83 or product CHOP regimen, every 3 weeks, for six cycles. Rituximab levels...

10.1007/s00280-018-3524-9 article EN cc-by Cancer Chemotherapy and Pharmacology 2018-01-23
Dmytro Trukhin Elena Poddubskaya Zoran Andrić Tamta Makharadze Ravi Shankar Bellala and 93 more Chaiyut Charoentum Eduardo Patricio Yanez Ruiz Andrea Fülöp Irfhan Ali Hyder Ali Kostas Syrigos Nuran Katgı Yamil Alonso Lopez Chuken Ilieva Rumyana Jasmin Reyes-Igama Rita de Cassia Costamilan Ana Del Campo García Amalia Florez Alexandra Paravisini Susana Millán Luiz H. Araujo Carla Maria de Oliveira Ferreira Hélio Pinczowski Maria Marcela Fernandes Monteiro Assen Dudov Janeta Syrova Francisco Javier Orlandi Jorquera Carlos Eduardo Gallardo Arenada Christian Lorenzo Caglevic Medina Davit Giorgadze Nino Mchedlidze Vladimer Kuchava Tamar Melkadze Amiran Matitashvili Nana Chikhladze E Samantas Theodoros Kontakiotis Beatrix Bálint Balazs Medgyasszay Eszter Csánky Shailesh Bondarde Lovenish Goyal Ajay Sharma Baijumon Balan Prabrajya Narayan Mohapatra Kaushalkumar Babubhai Patel Sachin Sharadchandra Hingmire Mithun Satish Shah Kartikeya Jain Ashish Agrawal Prashant Kumbhaj Asis Mukhopadhyay Paul Khoueiry Suhana Yusak Yong Kek Pang V. Pei Jye Prathepamalar Yehgambaram Fuad Ismail Gokula Kumar Appalanaido Feliciano Barrón Ma. Noemi Uy Felycette Gay Martinez-Lapus Maria Belen Tamayo Jennifer Sandoval-Tan Jamela Anne Osorio Sanchez Christina G. Galvez Josephine Contreras-Tolentino Evgeny Ledin Daniil Stroyakovskiy I. V. Kudryavtsev Vladimir Vladimirov Evgeniy Gotovkin М. В. Шомова Guzel Mukhametshina Igor Lifirenko Nina Karaseva M. Nechaeva Anna V. Tarasova Alexander Luft Lyudmila Kuzina Marina Petrović Milan Rančić Borjan Zaric Manoch Buranachokphaisan Sarayut Lucien Geater Ekkapong Tharavichitkul Mahmut Gümüş Igor Bondarenko Yaroslav Shparyk Serhii Shevnia Iryna Lytvyn Oleksii Kolesnik Yevhen Hotko Ivan Sinielnikov Hryhoriy Adamchuk Grygorii Ursol О. І. Іващук Yuriy Ostapenko Tetiana Popovska

MB02 (bevacizumab biosimilar) showed similar structural, functional, and pharmacokinetic properties to reference bevacizumab (Avastin®; EU-bevacizumab). To confirm clinical similarity between EU-bevacizumab, a comparability study was undertaken in the first-line treatment of stage IIIB/IV non-squamous non-small cell lung cancer (NSCLC). This multinational, double-blind, randomized, phase III (STELLA) compared or EU-bevacizumab (15 mg/kg) administered with chemotherapy (paclitaxel 200 mg/m2...

10.1007/s40259-021-00483-w article EN cc-by-nc BioDrugs 2021-04-29

Abstract Purpose MB02 is a biosimilar to bevacizumab that has demonstrated similar physicochemical and functional properties in vitro studies the reference (Avastin ® ). This study aims assess pharmacokinetic (PK) similarity of Japanese population. Methods double-blind, randomized, parallel-group, single-dose PK study, was performed healthy male volunteers. Subjects were equally randomized (1:1) receive single (3 mg/kg) IV dose or bevacizumab. assessments done up 70 days post-dose....

10.1007/s00280-021-04324-z article EN cc-by Cancer Chemotherapy and Pharmacology 2021-07-16

We conducted a randomized, crossover study in 23 healthy young female volunteers to compare the bioavailability of two brands meloxicam (7.5 mg) tablets and obtain pharmacokinetic parameters this molecule Mexican population not reported previously. Two (15 were administered as single dose on 2 treatment days separated by 1-week washout period. After dosing, serial blood samples collected for period 72 h. Plasma harvested was analyzed modified validated high-performance liquid chromatography...

10.1002/bdd.446 article EN Biopharmaceutics & Drug Disposition 2005-04-19

To evaluate the bioequivalence between two 250 mg-tablets of lysine clonixinate, Dorixina Forte (Siegfried Rhein, México) as reference product, and Prestodol (Farmaceúticos Rayere, S.A., test formulation.26 healthy adult female Mexican volunteers received a single oral dose 250-mg clonixinate under fasting conditions. The drug was administered following randomized, two-period, two-sequence, cross-over design. Twelve serial blood samples were collected up to 8 h after dosing, clonixin (CLX)...

10.5414/cpp48349 article EN International Journal of Clinical Pharmacology and Therapeutics 2010-05-01

Background: Patients with spinal cord injury (SCI) are at increased risk of renal insufficiency, so their function must regularly be monitored. Glomerular filtration rate (GFR) assessment is challenging as it requires measuring clearance exogenous markers, which impractical in most clinical settings. Thus, equations have been formulated to estimate GFR that utilize serum creatinine (Cr) or cystatin C (CysC). Objectives: Given loss muscle mass after SCI, we hypothesized using CysC would more...

10.46292/sci24-00001 article EN Topics in Spinal Cord Injury Rehabilitation 2024-11-01

Resumen.-OBJETIVO: Presentar un caso de rabdomiosarcoma paratesticular derecho en adulto joven 21 años edad.MÉTODOS: Tras realizar tratamiento con orquiectomía radical derecha vía inguinal, que se clasifica dentro del grupo clínico IA según el IRS -III (enfermedad localizada completamente resecada), complementa vincristina y actinomicina-D.RESULTADOS/CONCLUSIONES: Encontrándose libre enfermedad a los 18 meses la intervención quirúrgica.Destacando importancia adyuvante evolución posterior tumoral.

10.4321/s0004-06142005000200010 article ES cc-by-nc Archivos Españoles de Urología 2005-03-01

<h3>Background</h3> The use of biological treatments for psoriasis involves a significant improvement in disease management. However, the economic impact its on health systems is high. Optimised treatment patterns therapies, clinically controlled patients, attempt to find more efficient these drugs. <h3>Purpose</h3> To analyse patients with an optimised pattern and estimate annual saving third-level hospital. <h3>Material methods</h3> Observational, retrospective longitudinal study treated...

10.1136/ejhpharm-2019-eahpconf.15 article EN 2019-03-01
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