Evidence map›Paper›PMID 40757641›Full record

ReviewBiotechnology and bioengineering2025

Host Cell Protein Clinical Safety Risk Assessment-An Updated Industry Review.

Lisette Coye, Marisa A Jones, Georgeen Gaza-Bulseco, Carmelata Chitikila, Severine Clavier, Delphine Fougeron, Christine Grimaldi, Karen Hurkmans, Richard Hutchinson, Brenda Kellogg and 10 more

Abstract readReview
In one paragraph

Review in Biotechnology and bioengineering, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. 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

20 authors.

Lisette CoyePfizer Inc., Pharmaceutical Sciences, Bothell, Washington, USA.
Marisa A JonesGSK, Collegeville, Pennsylvania, USA.
Georgeen Gaza-BulsecoAbbVie Bioresearch Center, Analytical Development, Worcester, Massachusetts, USA.
Carmelata ChitikilaJohnson & Johnson, Therapeutics Development and Supply, Analytical Development, Malvern, Pennsylvania, USA.
Severine ClavierSanofi R&D, BioAnalytics, Global CMC Development, Vitry-sur-seine, France.ORCID https://orcid.org/0000-0001-5938-2144
Delphine FougeronSanofi R&D, BioAnalytics, Global CMC Development, Vitry-sur-seine, France.
Christine GrimaldiRegeneron Pharmaceuticals Inc., Tarrytown, New York, USA.ORCID https://orcid.org/0000-0002-5915-4317
Karen HurkmansAbbVie Bioresearch Center, Analytical Development, Worcester, Massachusetts, USA.
Richard HutchinsonJohnson & Johnson, Spring House, Pennsylvania, USA.ORCID https://orcid.org/0000-0002-9564-6407
Brenda KelloggTakeda Development Centre Americas Inc., Cambridge, Massachusetts, USA.
Xinrong LiuMural Oncology Inc., Waltham, Massachusetts, USA.
Nisha PalackalRegeneron Pharmaceuticals Inc., Tarrytown, New York, USA.ORCID https://orcid.org/0009-0004-7449-8953
Mahima TankTakeda Development Centre Americas Inc., Cambridge, Massachusetts, USA.
Pascal ValaxMerck KGaA - Darmstadt, Germany - Drug Substance Development, Merck BioDevelopment, Martillac, France.
Thomas WaernerBoehringer Ingelheim Pharma, GmbH & Co. KG, Analytical Development, Biologicals, Biberach, Germany.ORCID https://orcid.org/0000-0003-4298-1292
Fengqiang WangMerck & Co. Inc., Analytical R&D, Rahway, New Jersey, USA.ORCID https://orcid.org/0000-0002-8487-5159
Ying ZhangSarepta Therapeutics, Analytical Development and Quality Control, Bedford, Massachusetts, USA.
Yiwei ZhaoMural Oncology Inc., Waltham, Massachusetts, USA.
Sapphire SloanBioPhorum, Development Group, London, UK.ORCID https://orcid.org/0009-0007-9622-5317
Christina Zuch de ZafraPfizer Inc., Drug Safety Research & Development, South San Francisco, California, USA.ORCID https://orcid.org/0000-0001-9955-457X

Funding

Financial support for this manuscript was provided by BioPhorum Operations Group.
6 · The paper itself

Abstract

Host cell proteins (HCP) are process-related impurities that can co-purify with therapeutic proteins. Some HCP impurities potentially can have an impact on patient safety (immunogenicity or toxicity), efficacy, and/or product quality. It is important to reduce the levels of HCP impurities with a well-controlled manufacturing process and to monitor levels with a suitable analytical assay. Biopharmaceutical companies are now routinely using mass spectrometry to identify HCPs which are present in process intermediates and potentially in bulk drug substances and using the data to make decisions to continuously improve their processes and mitigate the potential risk to patients. Some companies perform identification of HCPs starting from the nonclinical stage of development, while others perform HCP identification at later stages or as a part of root cause analysis for identified HCP ELISA-related issues, process, and product quality or safety concerns. No matter the approach, a comprehensive risk assessment framework for identified HCPs is needed to support decision-making during development and is expected by regulators to ensure a safe and efficacious drug product. In this paper the BioPhorum Development Group HCP Workstream has brought together a team of industry experts to build upon existing risk assessment frameworks (e.g., de Zafra et al., 2015) and developed recommendations for assessment of clinical safety risks upon identification of individual HCPs, incorporating regulatory considerations and industry experience and using a real-world case study to illustrate the use of the updated frameworks. Key recommendations include conducting clinical risk assessment alongside product quality risk assessment following individual HCP identification and quantitation; focusing on biological activity and immunogenicity for any HCPs of concern; and communicating and collaborating effectively across functions to enable a comprehensive risk assessment.

Indexed as

Biological ProductsDrug ContaminationDrug IndustryPatient SafetyHumansRisk AssessmentBiological Productsclinical safety riskhigh‐risk HCPshost cell proteinsimmunogenicityMS/HCP‐MSPLBL2risk assessment

Identifiers

PMID40757641
PMCPMC12503010

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

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.