Evidence map›Paper›PMID 42867729›Full record

ReviewAAPS PharmSciTech2026

Antibody-Drug Conjugate Manufacturing: Facility Design, Process Safety, and Regulatory Considerations.

Ashley Harp

Abstract readReview
PubMed Publisher
In one paragraph

Review in AAPS PharmSciTech, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

1 author.

Ashley HarpCRB, 110 Washington Street, Suite 600, Conshohocken, 19428, PA, USA. ashley.harp@crbgroup.com.ORCID http://orcid.org/0009-0007-7670-3158

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This paper presents an in-depth examination of the manufacturing, formulation, and fill/finish processes for traditional antibody-drug conjugates (ADCs), with particular emphasis on cytotoxic ADCs and the unique risks associated with their production. ADCs inherent toxicity demands rigorous facility and equipment design, proactive risk assessment, and robust risk mitigation strategies. We describe the multiple processes and facility types involved in producing ADCs, with a more detailed focus on drug product facilities. In addition, we study the critical facility risk areas encountered and effective strategies for managing and overcoming those risks. While it is well understood that containment is a critical risk area in the ADC modality, there has been a significant amount of work published with respect to specific containment strategies and solutions for unique unit operations and this area has only been summarized in this review. The paper also addresses regulatory compliance-highlighting EU GMP Annex 1 expectations-and underscores the importance of robust containment strategies and holistic design elements for preventing cross contamination, personnel exposure, and mitigating environmental impact.

Indexed as

ImmunoconjugatesAnimalsAntibodies, MonoclonalChemistry, PharmaceuticalDrug IndustryFacility Design and ConstructionHumansRisk AssessmentTechnology, PharmaceuticalAntibodies, MonoclonalImmunoconjugatesantibody–drug conjugatesaseptic processingcollaborationfacility designlyophilizationmanufacturabilityoccupational safetysustainability

Identifiers

What OpenQuestion holds

Textmetadata
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.