Evidence map›Paper›PMID 37631301›Full record

ArticlePharmaceutics2023

Satisfying QTPP of Erythropoietin Biosimilar by QbD through DoE-Derived Downstream Process Engineering.

Kakon Nag, Enamul Haq Sarker, Samir Kumar, Sourav Chakraborty, Maksusdur Rahman Khan, Mashfiqur Rahman Chowdhury, Rony Roy, Ratan Roy, Bipul Kumar Biswas, Emrul Hasan Bappi and 2 more

Abstract read
In one paragraph

Article in Pharmaceutics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–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

1 citing paper in PubMed.

  1. 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

12 authors.

Kakon NagGlobe Biotech Limited, 3/Ka (New), Tejgaon I/A, Dhaka 1208, Bangladesh.
Enamul Haq SarkerGlobe Biotech Limited, 3/Ka (New), Tejgaon I/A, Dhaka 1208, Bangladesh.
Samir KumarGlobe Biotech Limited, 3/Ka (New), Tejgaon I/A, Dhaka 1208, Bangladesh.
Sourav ChakrabortyGlobe Biotech Limited, 3/Ka (New), Tejgaon I/A, Dhaka 1208, Bangladesh.
Maksusdur Rahman KhanGlobe Biotech Limited, 3/Ka (New), Tejgaon I/A, Dhaka 1208, Bangladesh.
Mashfiqur Rahman ChowdhuryGlobe Biotech Limited, 3/Ka (New), Tejgaon I/A, Dhaka 1208, Bangladesh.
Rony RoyGlobe Biotech Limited, 3/Ka (New), Tejgaon I/A, Dhaka 1208, Bangladesh.ORCID 0000-0002-4876-278X
Ratan RoyGlobe Biotech Limited, 3/Ka (New), Tejgaon I/A, Dhaka 1208, Bangladesh.
Bipul Kumar BiswasGlobe Biotech Limited, 3/Ka (New), Tejgaon I/A, Dhaka 1208, Bangladesh.
Emrul Hasan BappiGlobe Biotech Limited, 3/Ka (New), Tejgaon I/A, Dhaka 1208, Bangladesh.
Mohammad MohiuddinGlobe Biotech Limited, 3/Ka (New), Tejgaon I/A, Dhaka 1208, Bangladesh.
Naznin SultanaGlobe Biotech Limited, 3/Ka (New), Tejgaon I/A, Dhaka 1208, Bangladesh.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Well-characterized and scalable downstream processes for the purification of biologics are extremely demanding for delivering quality therapeutics to patients at a reasonable price. Erythropoietin (EPO) is a blockbuster biologic with diverse clinical applications, but its application is limited to financially well-off societies due to its high price. The high price of EPO is associated with the technical difficulties related to the purification challenge to obtain qualified products with a cost-effective defined process. Though there are reports for the purification of EPO there is no report of a well-characterized downstream process with critical process parameters (CPPs) that can deliver EPO consistently satisfying the quality target product profile (QTPP), which is a critical regulatory requirement. To advance the field, we applied the quality by design (QbD) principle and design of experiment (DoE) protocol to establish an effective process, which is scalable up to 100× batch size satisfying QTPP. We have successfully transformed the process from static mode to dynamic mode and validated it. Insignificant variation (

Indexed as

biosimilarcritical process parameter (CPP)design of experiment (DoE)downstreamerythropoietinprocess engineeringpurificationquality by design (QbD)quality target product profile (QTPP)validation

Identifiers

PMID37631301
PMCPMC10460001

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Registered trials

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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.