Evidence map›Paper›PMID 39545074›Full record

ReviewBioengineering & translational medicine2024

Antibody drug conjugates in the clinic.

Edidiong Udofa, Disha Sankholkar, Samir Mitragotri, Zongmin Zhao

Abstract readReview
In one paragraph

Review in Bioengineering & translational medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Review
  5. Review
  6. A review of targeted drug delivery with antibody-drug complexes.The Journal of pharmacology and experimental therapeutics · 2025
    Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Antibody drug conjugates in the clinic.Bioengineering & translational medicine · 2024
    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

4 authors.

Edidiong UdofaDepartment of Pharmaceutical Sciences University of Illinois Chicago Chicago Illinois USA.ORCID https://orcid.org/0000-0002-2164-1136
Disha SankholkarUniversity of Michigan Ann Arbor Ann Arbor Michigan USA.
Samir MitragotriJohn A. Paulson School of Engineering and Applied Sciences Harvard University Cambridge Massachusetts USA.ORCID https://orcid.org/0000-0002-2459-8305
Zongmin ZhaoDepartment of Pharmaceutical Sciences University of Illinois Chicago Chicago Illinois USA.ORCID https://orcid.org/0000-0001-8979-844X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antibody-drug conjugates (ADCs), chemotherapeutic agents conjugated to an antibody to enhance their targeted delivery to tumors, represent a significant advancement in cancer therapy. ADCs combine the precise targeting capabilities of antibodies and the potent cell-killing effects of chemotherapy, allowing for enhanced cytotoxicity to tumors while minimizing damage to healthy tissues. Here, we provide an overview of the current clinical landscape of ADCs, highlighting 11 U.S. Food and Drug Administration (FDA)-approved products and discussing over 500 active clinical trials investigating newer ADCs. We also discuss some key challenges associated with the clinical translation of ADCs and highlight emerging strategies to overcome these hurdles. Our discussions will provide useful guidelines for the future development of safer and more effective ADCs for a broader range of indications.

Indexed as

ADCantibodyantibody–drug conjugatecancercancer treatmentchemotherapyclinicclinical translationclinical trialdrug deliveryFDA

Identifiers

PMID39545074
PMCPMC11558205

What OpenQuestion holds

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LicenceCC BY
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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.