Evidence map›Paper›PMID 32796549›Full record

ReviewInternational journal of environmental research and public health2020

Clinical and Regulatory Concerns of Biosimilars: A Review of Literature.

Vesa Halimi, Armond Daci, Katerina Ancevska Netkovska, Ljubica Suturkova, Zaheer-Ud-Din Babar, Aleksandra Grozdanova

Abstract readReview
In one paragraph

Review in International journal of environmental research and public health, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 3 pooled it
–field-weighted citation impact
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

29 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Review
  5. Article
  6. Article
  7. Review
  8. Biosimilars for Australian Dermatologists.The Australasian journal of dermatology · 2025
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
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  20. Review
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

6 authors.

Vesa HalimiFaculty of Pharmacy, University Ss. Cyril and Methodius, 1000 Skopje, North Macedonia.
Armond DaciDepartment of Pharmacy, Faculty of Medicine, University of Prishtina, 10000 Prishtina, Kosovo.ORCID 0000-0003-1276-4561
Katerina Ancevska NetkovskaFaculty of Pharmacy, University Ss. Cyril and Methodius, 1000 Skopje, North Macedonia.
Ljubica SuturkovaFaculty of Pharmacy, University Ss. Cyril and Methodius, 1000 Skopje, North Macedonia.
Zaheer-Ud-Din BabarDepartment of Pharmacy, University of Huddersfield, Huddersfield, West Yorkshire HD1 3DH, UK.ORCID 0000-0003-1051-3240
Aleksandra GrozdanovaFaculty of Pharmacy, University Ss. Cyril and Methodius, 1000 Skopje, North Macedonia.ORCID 0000-0002-0098-8691

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although biosimilars have been part of clinical practice for more than a decade, healthcare professionals (HCPs) do not fully accept them. This is because of the perception that biosimilars may not be like their originators in terms of quality, safety, and efficacy. This study aims to evaluate the current knowledge and attitudes of healthcare professionals toward biosimilar prescription, and to elaborate on their concerns. We reviewed the literature using PubMed, Cochrane Library, and Science Direct electronic databases in the period from 2018 to 2020. The knowledge and confidence of healthcare professionals vary between countries, between clinical profiles and between studies. Although most of the healthcare professionals had a positive attitude to prescribing biosimilars, they would still prefer to prescribe them in initial treatment. Generally, HCPs were against multiple switches and substitution of biosimilars at the pharmacy level. HCP's key concern was interchangeability, with eventual consequences on the clinical outcome of patients. HCPs still approach biosimilars with caution and stigma. HCPs need to have an unbiased coherent understanding of biosimilars at clinical, molecular and regulatory levels. It was also observed that most of their concerns are more theoretical than science-based. Physicians are in an excellent position to accept biosimilars, but they need the additional support of regulatory authorities to approve and take into consideration the available scientific data regarding biosimilars.

Indexed as

Attitude of Health PersonnelBiosimilar PharmaceuticalsHealth PersonnelHumansPhysiciansBiosimilar Pharmaceuticalsbiosimilarsclinical practiceconfidenceeducationextrapolationinterchangeabilityknowledgepharmacovigilanceregulatory

Identifiers

PMID32796549
PMCPMC7460311

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.