Evidence map›Paper›PMID 26075238›Full record

ArticleBioMed research international2015

Physicochemical and biological characterization of a biosimilar trastuzumab.

Carlos A López-Morales, Mariana P Miranda-Hernández, L Carmina Juárez-Bayardo, Nancy D Ramírez-Ibáñez, Alexis J Romero-Díaz, Nelly Piña-Lara, Víctor R Campos-García, Néstor O Pérez, Luis F Flores-Ortiz, Emilio Medina-Rivero

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.4field-weighted citation impact, top 20% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Laboratory Scale Production and Purification of a Therapeutic Antibody.Journal of visualized experiments : JoVE · 2017
    Article
  6. Article
  7. Assessing Analytical Similarity of Proposed Amgen Biosimilar ABP 501 to Adalimumab.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2016
    Article
  8. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Carlos A López-MoralesUnidad de Investigación y Desarrollo, Probiomed S.A. de C.V., Cruce de Carreteras Acatzingo-Zumpahuacán s/n, 52400 Tenancingo, MEX, Mexico.
Mariana P Miranda-HernándezUnidad de Investigación y Desarrollo, Probiomed S.A. de C.V., Cruce de Carreteras Acatzingo-Zumpahuacán s/n, 52400 Tenancingo, MEX, Mexico.
L Carmina Juárez-BayardoUnidad de Investigación y Desarrollo, Probiomed S.A. de C.V., Cruce de Carreteras Acatzingo-Zumpahuacán s/n, 52400 Tenancingo, MEX, Mexico.
Nancy D Ramírez-IbáñezUnidad de Investigación y Desarrollo, Probiomed S.A. de C.V., Cruce de Carreteras Acatzingo-Zumpahuacán s/n, 52400 Tenancingo, MEX, Mexico.
Alexis J Romero-DíazUnidad de Investigación y Desarrollo, Probiomed S.A. de C.V., Cruce de Carreteras Acatzingo-Zumpahuacán s/n, 52400 Tenancingo, MEX, Mexico.
Nelly Piña-LaraUnidad de Investigación y Desarrollo, Probiomed S.A. de C.V., Cruce de Carreteras Acatzingo-Zumpahuacán s/n, 52400 Tenancingo, MEX, Mexico.
Víctor R Campos-GarcíaMUHC Research Institute, Royal Victoria Hospital, McGill University, 687 Pine Avenue West, Montreal, QC, Canada H3A 1A1.
Néstor O PérezUnidad de Investigación y Desarrollo, Probiomed S.A. de C.V., Cruce de Carreteras Acatzingo-Zumpahuacán s/n, 52400 Tenancingo, MEX, Mexico.
Luis F Flores-OrtizUnidad de Investigación y Desarrollo, Probiomed S.A. de C.V., Cruce de Carreteras Acatzingo-Zumpahuacán s/n, 52400 Tenancingo, MEX, Mexico.
Emilio Medina-RiveroUnidad de Investigación y Desarrollo, Probiomed S.A. de C.V., Cruce de Carreteras Acatzingo-Zumpahuacán s/n, 52400 Tenancingo, MEX, Mexico.ORCID 0000-0001-8862-1378
Royal Victoria Hospital · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

According to the World Health Organization, the incidence of malignant neoplasms and endocrine, blood, and immune disorders will increase in the upcoming decades along with the demand of affordable treatments. In response to this need, the development of biosimilar drugs is increasing worldwide. The approval of biosimilars relies on the compliance with international guidelines, starting with the demonstration of similarity in their physicochemical and functional properties against the reference product. Subsequent clinical studies are performed to demonstrate similar pharmacological behavior and to diminish the uncertainty related to their safety and efficacy. Herein we present a comparability exercise between a biosimilar trastuzumab and its reference product, by using a hierarchical strategy with an orthogonal approach, to assess the physicochemical and biological attributes with potential impact on its pharmacokinetics, pharmacodynamics, and immunogenicity. Our results showed that the high degree of similarity in the physicochemical attributes of the biosimilar trastuzumab with respect to the reference product resulted in comparable biological activity, demonstrating that a controlled process is able to provide consistently the expected product. These results also constitute the basis for the design of subsequent delimited pharmacological studies, as they diminish the uncertainty of exhibiting different profiles.

Indexed as

Antineoplastic AgentsBiosimilar PharmaceuticalsTrastuzumabCell Line, TumorDrug Screening Assays, AntitumorHumansAntineoplastic AgentsBiosimilar PharmaceuticalsTrastuzumab

Identifiers

PMID26075238
PMCPMC4449878
OpenAlexW1572610401

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.