Evidence map›Paper›PMID 40841178›Full record

ArticleClinical and translational science2025

Model-Informed Optimal Dosing of Anti-CD47 Antibody Using Target-Mediated Drug Disposition Model.

Seongmee Jeong, Sung Young Lee, Sung Ho Kim, Heung Tae Kim, Hwi-Yeol Yun, Jung-Woo Chae, Soyoung Lee

Registry-linked trialAbstract readClinical Trial, Phase I
In one paragraph

Article in Clinical and translational science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05276310 (An Open-Label, Dose-Escalation and Expansion, Phase I Study to Investigate the Safety, Tolerability, Pharmacokinetics, and Clinical Activity of IMC-002 in Patients With Advanced Cancer Failed to Standard Therapy), which is not on this 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.

NCT05276310 phase1recruitingnot on this map

An Open-Label, Dose-Escalation and Expansion, Phase I Study to Investigate the Safety, Tolerability, Pharmacokinetics, and Clinical Activity of IMC-002 in Patients With Advanced Cancer Failed to Standard Therapy

TypeinterventionalSponsorImmuneOncia Therapeutics Inc.Ran2022 to 2029Enrolled62ConditionsAdvanced CancerArmsIMC-002
3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

7 authors.

Seongmee JeongCollege of Pharmacy, Chungnam National University, Daejeon, Republic of Korea.ORCID 0009-0005-0005-6535
Sung Young LeeImmuneOncia Therapeutics, Inc., Seoul, Republic of Korea.
Sung Ho KimImmuneOncia Therapeutics, Inc., Seoul, Republic of Korea.
Heung Tae KimImmuneOncia Therapeutics, Inc., Seoul, Republic of Korea.
Hwi-Yeol YunCollege of Pharmacy, Chungnam National University, Daejeon, Republic of Korea.ORCID 0000-0001-8793-2449
Jung-Woo ChaeCollege of Pharmacy, Chungnam National University, Daejeon, Republic of Korea.ORCID 0000-0001-6026-7063
Soyoung LeeCollege of Pharmacy, Chungnam National University, Daejeon, Republic of Korea.ORCID 0000-0001-5799-4489

Funding

Chungnam National University, Institute of Information & Communications Technology Planning Evaluation (IITP) RS-2022-00155857Korea Environmental Industry & Technology Institute (KEITI) RS-2021-KE001333Korea Health Industry Development Institute (KHIDI) RS-2024-00336984Korea Health Industry Development Institute (KHIDI) RS-2025-02306055Korea Institute for Advancement of Technology (KIAT) RS-2024-00434342Korea Institute of Toxicology (KIT) 2710008763Korea Institute of Toxicology (KIT) KK-2401-01Ministry of Health & Welfare and Ministry of Science and ICT RS-2024-00460694National Research Foundation of Korea (NRF) RS-2022-NR069643National Research Foundation of Korea (NRF) RS-2022-NR070856National Research Foundation of Korea (NRF) RS-2023-00278597
6 · The paper itself

Abstract

IMC-002, an anti-cluster of differentiation 47 (CD47) antibody, was developed as a fully human immunoglobulin (Ig) G4 monoclonal antibody targeting CD47. IMC-002 blocks CD47-signal regulatory protein alpha (SIRPα) interactions, increasing the phagocytosis of cancer cells by macrophages. This study established a target-mediated drug disposition (TMDD) pharmacokinetics (PK) model for IMC-002 to explain the characteristics of the neonatal Fc receptor (FcRn) of IgG based on phase I

Indexed as

Antibodies, MonoclonalCD47 AntigenModels, BiologicalNeoplasmsAdultAgedDose-Response Relationship, DrugFemaleHistocompatibility Antigens Class IHumansImmunoglobulin GInfusions, IntravenousMaleMiddle AgedReceptors, FcAntibodies, MonoclonalCD47 AntigenCD47 protein, humanFc receptor, neonatalHistocompatibility Antigens Class IImmunoglobulin GReceptors, Fcanti‐CD47 antibodymodel‐informed optimal dosingtarget‐mediated drug disposition model (TMDD)

Identifiers

PMID40841178
PMCPMC12370379

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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.