Evidence map›Paper›PMID 39979532›Full record

ArticlePharmaceutical research2025

In vitro Stability Study of a Panel of Commercial Antibodies at Physiological pH and Temperature as a Guide to Screen Biologic Candidate Molecules for the Potential Risk of In vivo Asparagine Deamidation and Activity Loss.

Richa Garg, Sean McCarthy, Alayna George Thompson, Jiang Zhang, Emily Mattson, Anca Clabbers, Aimalohi Acquah, Jianwen Xu, Chen Zhou, Amr Ali and 2 more

Abstract read
In one paragraph

Article in Pharmaceutical research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
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  3. 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.

Richa GargBiologics CMC Drug Product Development, Preformulation, AbbVie, Worcester, MA, 01605, USA.
Sean McCarthyBiologics CMC Analytical Research and Development, Developability, AbbVie, Worcester, MA, 01605, USA.
Alayna George ThompsonBiologics CMC Analytical Research and Development, Developability, AbbVie, North Chicago, IL, 60064, USA.
Jiang ZhangAnalytical Development, Product Development Science & Technology, AbbVie, Worcester, MA, 01605, USA.
Emily MattsonBiomolecular Interaction Group, Protein Sciences, Biotherapeutics and Genetic Medicine, AbbVie, Worcester, MA, 01605, USA.
Anca ClabbersBiomolecular Interaction Group, Protein Sciences, Biotherapeutics and Genetic Medicine, AbbVie, Worcester, MA, 01605, USA.
Aimalohi AcquahBiologics CMC Drug Product Development, Preformulation, AbbVie, Worcester, MA, 01605, USA.
Jianwen XuBiologics CMC Drug Product Development, Preformulation, AbbVie, Worcester, MA, 01605, USA.
Chen ZhouBiologics CMC Drug Product Development, Preformulation, AbbVie, Worcester, MA, 01605, USA.
Amr AliAnalytical Development, Product Development Science & Technology, AbbVie, Worcester, MA, 01605, USA.
Dana FilotiBiologics CMC Analytical Research and Development, Developability, AbbVie, Worcester, MA, 01605, USA.
Rajeeva SinghBiologics CMC Drug Product Development, Preformulation, AbbVie, Worcester, MA, 01605, USA. rajeeva.singh@abbvie.com.ORCID http://orcid.org/0000-0002-1537-6209

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveBiologic drug molecules such as antibodies are exposed to the physiological stress conditions of pH 7.4 and 37°C during their long circulation lifetime in vivo. The stress on biologic molecules in vivo is more severe compared to that under typical storage conditions of low pH formulation and cold temperature. Chemical degradation of critical residues such as asparagine may occur in vivo, leading to potential loss of biological activity. This study describes a physiologically relevant and convenient in vitro PBS stress condition of pH 7.4 and 40°C for pre-clinical stability screening of biologic molecules.

methodsAs benchmarks, multiple commercial antibodies (alirocumab, evolocumab, golimumab, ramucirumab, and trastuzumab) were tested in parallel for formulation stability at storage and accelerated temperature conditions and for physiological stability at pH 7.4 and 40°C stress both for 3-4 weeks. The stressed antibodies were monitored for chemical modification and target binding, without requiring affinity purification.

resultsThe major CDR chemical modifications observed in PBS-stressed commercial antibodies were deamidations of asparagine residues. Although slight decreases in target binding were observed for two antibodies, the affinities overall remained strong after PBS stress.

conclusionsThis benchmarking study of commercial antibodies would be useful as a guide to screen discovery-stage biologic molecules both for drug product stability at formulation pH under storage and accelerated temperature conditions and for physiological stability under in vivo-mimicking pH and temperature stress condition.

Indexed as

Antibodies, MonoclonalAsparagineDrug StabilityHumansHydrogen-Ion ConcentrationProtein StabilityTemperatureAntibodies, MonoclonalAsparagineantibodiesasparaginedeamidationPBSstress

Identifiers

PMID39979532
PMCPMC11880144

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Registered trials

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