Evidence map›Paper›PMID 37830579›Full record

ArticleCells2023

Early Pharmacodynamic Changes Measured Using RNA Sequencing of Peripheral Blood from Patients in a Phase I Study with Mitazalimab, a Potent CD40 Agonistic Monoclonal Antibody.

Hampus Andersson, Aastha Sobti, David Gomez Jimenez, Yago Pico de Coaña, Sumeet Vijay Ambarkhane, Karin Hägerbrand, Karin Enell Smith, Malin Lindstedt, Peter Ellmark

Registry-linked trialOpen access · goldAbstract readClinical Trial, Phase I
In one paragraph

Article in Cells, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02829099 (A Phase 1, Open-Label Study of the Safety, Pharmacokinetics and Pharmacodynamics of JNJ-64457107, an Agonistic Human Monoclonal Antibody Targeting CD40 in Patients With Advanced Stage Solid Tumors), which is not on this map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.6field-weighted citation impact, top 14% of its field
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.

NCT02829099 phase1completednot on this map

A Phase 1, Open-Label Study of the Safety, Pharmacokinetics and Pharmacodynamics of JNJ-64457107, an Agonistic Human Monoclonal Antibody Targeting CD40 in Patients With Advanced Stage Solid Tumors

TypeinterventionalSponsorJanssen Research & Development, LLCRan2016 to 2021Enrolled95ConditionsAdvanced Solid NeoplasmsArmsJNJ-64457107
3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Harnessing the potential of CD40 agonism in cancer therapy.Cytokine & growth factor reviews · 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

9 authors at 2 institutions in 1 country.

Hampus AnderssonAlligator Bioscience AB, 223 81 Lund, Sweden.ORCID 0009-0007-9517-5864
Aastha SobtiAlligator Bioscience AB, 223 81 Lund, Sweden.ORCID 0000-0001-5031-6052
David Gomez JimenezAlligator Bioscience AB, 223 81 Lund, Sweden.
Yago Pico de CoañaAlligator Bioscience AB, 223 81 Lund, Sweden.
Sumeet Vijay AmbarkhaneAlligator Bioscience AB, 223 81 Lund, Sweden.
Karin HägerbrandAlligator Bioscience AB, 223 81 Lund, Sweden.
Karin Enell SmithAlligator Bioscience AB, 223 81 Lund, Sweden.
Malin LindstedtAlligator Bioscience AB, 223 81 Lund, Sweden.
Peter EllmarkAlligator Bioscience AB, 223 81 Lund, Sweden.ORCID 0000-0002-6687-1250
Alligator Bioscience (Sweden) · SELund University · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

CD40-targeting therapies can enhance the dendritic cell priming of tumor-specific T cells and repolarize intratumoral macrophages to alleviate the tumoral immunosuppressive environment and remodel the extracellular matrix. Mitazalimab is a potent agonistic CD40 monoclonal IgG1 antibody currently under clinical development. This study used RNA sequencing of blood samples from a subset of patients from a Phase I trial with mitazalimab (NCT02829099) to assess peripheral pharmacodynamic activity. We found that mitazalimab induced transient peripheral transcriptomic alterations (at 600 µg/kg and 900 µg/kg dose administered intravenously), which mainly were attributed to immune activation. In particular, the transcriptomic alterations showed a reduction in effector cells (e.g., CD8

Indexed as

Antibodies, MonoclonalAntibodies, Monoclonal, HumanizedCD8-Positive T-LymphocytesNeoplasmsCD40 AntigensHumansSequence Analysis, RNAAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedCD40 AntigensmitazalimabcancerCD40mitazalimabpharmacodynamicsRNA sequencing

Identifiers

PMID37830579
PMCPMC10572020
OpenAlexW4387101333

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.