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Study identifier: NCT05978492 Synced from ClinicalTrials.gov · August 08, 2026
● Study status: Recruiting

A Study of TXN10128 in Subjects With Solid Tumors

Condition: Locally Advanced (Unresectable) or Metastatic Solid Tumors  ·  Sponsor: Txinno Bioscience Inc.

PhasePhase 1
Planned participants96
Who can joinAll sexes, 19 Years to no upper limit
Healthy volunteersNoCheck eligibility criteria ↓
Where6 locations

Interested? Contact the study team ↓

Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.

About this study

This is a phase I clinical trial to primarily evaluate the safety, tolerability, and addtionally assess pharmacokinetics, pharmacodynamics, and antitumor activity of investigational product, TXN10128. The target subjects will be consisted of patients with locally advanced (unresectable) or metastatic soild tumors. This study includes a dose-escalation part and a dose-expansion part, and a TXN10128 monotherapy part and a TXN10128 + Irinotecan or Paclitaxel combination therapy part.

This description comes directly from the study's public registry record.

Talk to the study team

Eun-Young Kwak, Ph.D.  ·  82 31 778 8688  ·  bella@txinno.com

There is no obligation to join — the study team can answer your questions about taking part.

Always discuss trial participation with your own doctor first.

Full eligibility criteria (exactly as the study team wrote them)

Inclusion Criteria: * Male or female subjects ≥19 years of age at the time of informed consent. * Histologically and/or cytologically confirmed any progressive, locally advanced (unresectable), or metastatic solid tumors that have relapsed or are refractory following the last line of treatment and for which prior standard therapy has been ineffective, or standard therapy does not exist or is not considered appropriate. * ECOG performance status of 0 or 1. * Life expectancy of at least 12 weeks. Exclusion Criteria: * Has leptomeningeal disease. * Experienced a Grade ≥3 immune-related adverse events (irAE) with prior immunotherapy with the exception of non-clinically significant laboratory abnormalities. * Prior organ transplantation. * Known positive human immunodeficiency virus (HIV) infection.

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (6)

Seoul National University Bundang HospitalSeongnam-si, Gyeonggi-do, South KoreaRecruiting
Chungbuk National University HospitalCheonju, North Chungcheong, South KoreaRecruiting
Seoul National Univ. HospitalSeoul, Seoul, South KoreaRecruiting
Asan Medical CenterSeoul, Seoul, South KoreaRecruiting
Gachon University Gil Medical CenterIncheon, South KoreaRecruiting
SAMSUNG Medical CenterSeoul, South KoreaRecruiting

More studies in these areas

This study lists sites in the areas below. Each link shows other recruiting studies near that city, from the public registry record.

Seongnam-siCheonjuSeoulIncheon

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