Evidence map›Paper›PMID 41551730›Full record

ReviewTranslational and clinical pharmacology2025

A review of clinical pharmacology considerations in antibody-drug conjugates approved by the US Food and Drug Administration between 2000 and 2025.

Seoyoung Koo, Chae Yeon Kim, Jeong-Hyeon Lim, Eunyoung Lee, In Young Kim, Young G Shin, Hanlim Moon

Erratum issuedAbstract readReview
In one paragraph

Review in Translational and clinical pharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. 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.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Seoyoung KooMediRama, Inc., Seoul 06927, Korea.ORCID https://orcid.org/0009-0004-0455-8412
Chae Yeon KimDepartment of Medicine, Chosun University College of Medicine, Gwangju 61452, Korea.
Jeong-Hyeon LimCollege of Pharmacy, Chungnam National University, Daejeon 34134, Korea.
Eunyoung LeeMediRama, Inc., Seoul 06927, Korea.
In Young KimMediRama, Inc., Seoul 06927, Korea.
Young G ShinCollege of Pharmacy, Chungnam National University, Daejeon 34134, Korea.
Hanlim MoonMediRama, Inc., Seoul 06927, Korea.ORCID https://orcid.org/0000-0003-1241-0560

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antibody-drug conjugates (ADCs) represent a promising class of anticancer therapies with rapidly expanding development. However, regulatory approval remains complex due to their unique pharmacological properties. We systematically analyzed U.S. Food and Drug Administration (FDA)'s clinical pharmacology considerations across all approved ADCs to identify consistent regulatory patterns and inform future development strategies. We comprehensively reviewed 13 FDA-approved ADCs as of March 2025, examining clinical pharmacology and/or multidisciplinary reviews from Drugs@FDA. Six key parameters from the

Indexed as

Antibody-Drug Conjugate (ADC)Clinical PharmacologyDrug DevelopmentFood and Drug Administration (FDA)

Identifiers

PMID41551730
PMCPMC12806659

What OpenQuestion holds

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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.