Evidence map›Paper›PMID 40948459›Full record

ReviewmAbs2025

Mechanistic and predictive formulation development for viscosity mitigation of high-concentration biotherapeutics.

Matthew A Cruz, Marco Blanco, Iriny Ekladious

Abstract readReview
In one paragraph

Review in mAbs, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Viscosity of concentrated antibodies from a dynamic model of electrostatics.Proceedings of the National Academy of Sciences of the United States of America · 2025
    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

3 authors.

Matthew A CruzSterile Product Development, Merck & Co., Inc, Rahway, NJ, USA.ORCID 0000-0002-9270-3170
Marco BlancoDiscovery Pharmaceutical Sciences, Merck & Co., Inc, West Point, PA, USA.ORCID 0000-0001-5768-9038
Iriny EkladiousSterile Product Development, Merck & Co., Inc, Rahway, NJ, USA.ORCID 0000-0003-1192-1414

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Proteins are an important class of therapeutics for combatting a wide variety of diseases. The increasing demand for convenient, patient-centric treatment options has propelled the development of subcutaneously delivered protein therapies and increased the interest in novel formulations and delivery methods. However, subcutaneous delivery of protein therapeutics remains a challenge due to the high protein concentrations ( >100 mg/mL) required to circumvent lower bioavailability and the smaller injection volumes required to enable the use of mature and cost-effective devices, such as standard prefilled syringes and autoinjectors. At high concentrations, protein solutions exhibit elevated viscosity, which poses injectability and manufacturing challenges. Here, we review the state of the art in experimental and computationally predictive formulation development approaches for viscosity mitigation of high-concentration protein solution therapeutics, and we suggest new directions for expanding the utility of these approaches beyond traditional monoclonal antibodies. Innovative approaches should leverage and combine advances in both experimental and computational methods, including machine learning and artificial intelligence, to rapidly identify formulation compositions for viscosity reduction, and subsequently facilitate the development of patient-centric biotherapeutics.

Indexed as

Antibodies, MonoclonalBiological ProductsDrug CompoundingAnimalsHumansViscosityAntibodies, MonoclonalBiological ProductsArtificial intelligencebiologicsdevelopmentdrug productformulationhigh-concentrationmachine learningsubcutaneousviscosity

Identifiers

PMID40948459
PMCPMC12439579

What OpenQuestion holds

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LicenceCC BY-NC
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.