Evidence map›Paper›PMID 41542564›Full record

ArticlebioRxiv : the preprint server for biology2026

CD99Targeted Irinotecan Containing Nanoparticles Show Twenty-Fold Greater Anti-Tumor Effect Than Free Irinotecan For Treatment of Ewing Sarcoma.

Hyung-Gyoo Kang, Sheetal Mitra, Bryon Upton, Jean Parmentier, Anahit Hovsepyran, Jon Nagy, Timothy J Triche

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 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

7 authors.

Hyung-Gyoo KangChildren's Hospital Los Angeles, University of Southern California.
Sheetal MitraChildren's Hospital Los Angeles, University of Southern California.
Bryon UptonNanoValent Pharmaceuticals, Inc., University of Southern California.
Jean ParmentierChildren's Hospital Los Angeles, University of Southern California.
Anahit HovsepyranChildren's Hospital Los Angeles, University of Southern California.
Jon NagyNanoValent Pharmaceuticals, Inc., University of Southern California.
Timothy J TricheChildren's Hospital Los Angeles, University of Southern California.ORCID 0000-0001-5665-946X

Funding

Tumor Antigen Targeted Nanoparticle Therapy for Glioblastoma (GBM)R42CA281707 · NCI · NANOVALENT PHARMACEUTICALS, INC. · PI NAGY, JON OWEN, TRICHE, TIMOTHY J. · 2023 to 2025
$2.4M
NV103: Antibody Conjugated Nanoparticle for Ewing Sarcoma Targeted TherapyR44CA233128 · NCI · NANOVALENT PHARMACEUTICALS, INC. · PI NAGY, JON OWEN, TRICHE, TIMOTHY J. · 2018 to 2020
$2.2M
NCI NIH HHS R42 CA281707NCI NIH HHS R44 CA233128
6 · The paper itself

Abstract

Purpose: To assess the antitumor efficacy, pharmacokinetics, and safety of NV103, a CD99-targeted liposomal irinotecan nanoparticle, in a preclinical Ewing sarcoma model. Experimental Design: NV103 is a CD99-antibody targeted irinotecan containing nanoparticle, engineered to selectively deliver irinotecan to CD99 expressing tumor cells. Results: NV103 bound selectively to tumor cells (>80× over control), was rapidly internalized, and showed enhanced potency Conclusions: NV103 displays potent and durable antitumor activity in Ewing sarcoma at low doses with no toxicity and favorable pharmacokinetics. These findings support further development for clinical translation.

Identifiers

PMID41542564
PMCPMC12803216

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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.