Evidence map›Paper›PMID 40490502›Full record

ArticleBritish journal of cancer2025

GX-I7, a long-acting IL-7, safely and effectively increased peripheral CD8

Gun Min Kim, Sojeong Kim, Myung Ah Lee, Mi-Sun Byun, Donghoon Choi, Se Hwan Yang, JungWon Woo, Young Chul Sung, Eui-Cheol Shin, Su-Hyung Park and 2 more

Registry-linked trialAbstract readClinical Trial, Phase IMulticenter Study
In one paragraph

Article in British journal of cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03478995 (A Phase 1b, Open Label, Dose-escalation Study to Evaluate Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of GX-I7 in Patients With Locally Advanced or Metastatic Solid Tumors), which is not on this map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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.

NCT03478995 phase1completednot on this map

A Phase 1b, Open Label, Dose-escalation Study to Evaluate Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of GX-I7 in Patients With Locally Advanced or Metastatic Solid Tumors

TypeinterventionalSponsorGenexine, Inc.Ran2018 to 2020Enrolled35ConditionsLocally Advanced or Metastatic Solid TumorsArmsGX-I7
3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Journal of the American Chemical Society · 2025
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. 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

12 authors.

Gun Min Kim *Division of Medical Oncology, Department of Internal Medicine, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, Korea.
Sojeong Kim *Graduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology, Daejeon, Korea.
Myung Ah LeeDivision of Medical Oncology, Seoul St, Mary's Hospital, The catholic University of Korea, Seoul, Korea.
Mi-Sun ByunGenexine, Inc., Seoul, Korea.ORCID http://orcid.org/0000-0002-2303-2764
Donghoon ChoiNeoImmuneTech, Inc., Rockville, MD, USA.
Se Hwan YangNeoImmuneTech, Inc., Rockville, MD, USA.
JungWon WooGenexine, Inc., Seoul, Korea.
Young Chul SungGenexine, Inc., Seoul, Korea.
Eui-Cheol ShinGraduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology, Daejeon, Korea.
Su-Hyung ParkGraduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology, Daejeon, Korea. park3@kaist.ac.kr.ORCID http://orcid.org/0000-0001-6363-7736
Tae Won KimDepartment of Oncology, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Korea. twkimmd@amc.seoul.kr.ORCID http://orcid.org/0000-0001-9522-1997
Joohyuk SohnDivision of Medical Oncology, Department of Internal Medicine, Yonsei Cancer Center, Yonsei University College of Medicine, Seoul, Korea. ONCOSOHN@yuhs.ac.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGX-I7 (rhIL-7-hyFc, efineptakin alfa) is a hybrid Fc-fused long-acting interleukin-7 (IL-7) with the aim of correcting T-cell deficiency, thereby strengthening the immune response to fight against cancer. This Phase 1b, dose-escalation study was designed to assess the safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) of GX-I7 in patients with locally advanced or metastatic solid tumours.

methodsThis study, conducted in patients with advanced solid tumours at three hospitals in Korea, involved intramuscular GX-I7 administration across eight dose levels (60-1700 µg/kg) in 3- and 6-week cohorts. A dose-expansion phase at 720 and 1200 µg/kg further assessed GX-I7's safety and efficacy.

resultsAnti-tumour responses showed either stable disease (SD) or disease progression (PD). GX-I7 demonstrated dose-dependent increases in the maximum serum concentration (C DISCUSSION: Findings suggest GX-I7 is a safe T cell-amplifying agent with peripheral immune activation. Ongoing studies are exploring its ability to enhance immune responses in peripheral immune cells and tumour cells when combined with other anti-cancer agents. CLINICAL

trial registrationNCT03478995.

Indexed as

CD4-Positive T-LymphocytesCD8-Positive T-LymphocytesInterleukin-7Lymphocytes, Tumor-InfiltratingNeoplasmsAdultAgedFemaleHumansMaleMiddle AgedNeoplasm MetastasisIL7 protein, humanInterleukin-7

Identifiers

PMID40490502
PMCPMC12356974

What OpenQuestion holds

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LicenceCC BY
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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.