Evidence map›Paper›PMID 42713665›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026

Discovery and Optimization of AMT-676, a CDH17-Targeting ADC for the Treatment of Advanced Gastrointestinal Cancers.

Ying-Nan Wang, Dan-Yun Ruan, Jing Shi, Yue Huang, Hui Sheng, Ya-Ling Huang, Linjie Ma, Lijun Wang, Caiwei Chen, Yixuan Wang and 12 more

Registry-linked trialAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06400485 (First-in-Human, Phase I/II Study of AMT-676, an Anti CDH17 Antibody-Drug Conjugate, in Patients With Advanced Solid Tumors), which is not on this 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.

NCT06400485 early_phase1recruitingnot on this map

First-in-Human, Phase I/II Study of AMT-676, an Anti CDH17 Antibody-Drug Conjugate, in Patients With Advanced Solid Tumors

TypeinterventionalSponsorMultitude Therapeutics Inc.Ran2024 to 2027Enrolled24ConditionsAdvanced Solid TumorsArmsAMT-676
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

22 authors.

Ying-Nan Wang *Department of Medical Oncology, State Key Laboratory of Oncology in South China, Guangdong Provincial Clinical Research Center For Cancer, Sun Yat-Sen University Cancer Center, Sun Yat-Sen University, Guangzhou, People's Republic of China.ORCID https://orcid.org/0009-0004-1235-4452
Dan-Yun Ruan *Research Unit of Precision Diagnosis and Treatment for Gastrointestinal Cancer, Chinese Academy of Medical Sciences, Guangzhou, People's Republic of China.
Jing Shi *Multitude Therapeutics, Shanghai, People's Republic of China.
Yue Huang *Department of Medical Oncology, State Key Laboratory of Oncology in South China, Guangdong Provincial Clinical Research Center For Cancer, Sun Yat-Sen University Cancer Center, Sun Yat-Sen University, Guangzhou, People's Republic of China.
Hui ShengResearch Unit of Precision Diagnosis and Treatment for Gastrointestinal Cancer, Chinese Academy of Medical Sciences, Guangzhou, People's Republic of China.
Ya-Ling HuangMultitude Therapeutics, Shanghai, People's Republic of China.ORCID https://orcid.org/0009-0000-0410-1739
Linjie MaMultitude Therapeutics, Shanghai, People's Republic of China.
Lijun WangMultitude Therapeutics, Shanghai, People's Republic of China.
Caiwei ChenMultitude Therapeutics, Shanghai, People's Republic of China.
Yixuan WangMultitude Therapeutics, Shanghai, People's Republic of China.
Yue ZhangMultitude Therapeutics, Shanghai, People's Republic of China.
Yi ShenMultitude Therapeutics, Shanghai, People's Republic of China.
Qing ZhangMultitude Therapeutics, Shanghai, People's Republic of China.
Jianjian ZhangMultitude Therapeutics, Shanghai, People's Republic of China.
Yanfang TangMultitude Therapeutics, Shanghai, People's Republic of China.
Jin-Ling ZhangResearch Unit of Precision Diagnosis and Treatment for Gastrointestinal Cancer, Chinese Academy of Medical Sciences, Guangzhou, People's Republic of China.ORCID https://orcid.org/0000-0003-3419-6542
Jia-Jia HuResearch Unit of Precision Diagnosis and Treatment for Gastrointestinal Cancer, Chinese Academy of Medical Sciences, Guangzhou, People's Republic of China.ORCID https://orcid.org/0000-0002-0372-291X
Chen-Yi WuDepartment of Medical Oncology, State Key Laboratory of Oncology in South China, Guangdong Provincial Clinical Research Center For Cancer, Sun Yat-Sen University Cancer Center, Sun Yat-Sen University, Guangzhou, People's Republic of China.
Jia-Ying ChenDepartment of Medical Oncology, State Key Laboratory of Oncology in South China, Guangdong Provincial Clinical Research Center For Cancer, Sun Yat-Sen University Cancer Center, Sun Yat-Sen University, Guangzhou, People's Republic of China.ORCID https://orcid.org/0009-0006-8903-171X
Xun MengMultitude Therapeutics, Shanghai, People's Republic of China.
Shu-Hui LiuMultitude Therapeutics, Redwood City, California, USA.ORCID https://orcid.org/0000-0002-5221-6853
Feng WangDepartment of Medical Oncology, State Key Laboratory of Oncology in South China, Guangdong Provincial Clinical Research Center For Cancer, Sun Yat-Sen University Cancer Center, Sun Yat-Sen University, Guangzhou, People's Republic of China.ORCID https://orcid.org/0000-0001-7668-9674

Funding

New Cornerstone Science Foundation
6 · The paper itself

Abstract

Advanced-stage gastrointestinal (GI) cancers present an unmet need for innovative therapies, and antibody-drug conjugates (ADCs) offer promising solutions. This study investigates the antitumor efficacy and toxicity of AMT-676, a novel ADC targeting Cadherin 17 (CDH17), in GI cancers. Utilizing MabArray screening and immunohistochemistry, CDH17 was identified as a promising ADC target in GI tumors with minimal expression in healthy organs. The ADC was optimized through comprehensive in vitro and in vivo evaluations of binding affinity, cytotoxicity, pharmacokinetics, and toxicity, with antitumor potential evaluated using cell line-derived (CDX) and patient-derived tumor xenograft (PDX) models. Leveraging the T moiety-exatecan platform, we synthesized AMT-676, comprising a high-affinity CDH17-specific antibody, a hydrophilic self-immolative T1000 linker, and exatecan with a Drug-to-Antibody Ratio (DAR) of 4. AMT-676 demonstrated sustained antitumor responses across CDX and PDX GI models with diverse CDH17 expression, notably inhibiting metastatic growth in a colorectal cancer model. Cynomolgus monkey studies revealed favorable pharmacokinetics and manageable toxicity associated with AMT-676. In conclusion, we developed a novel CDH17-targeting ADC characterized by a high therapeutic index and tolerable toxicity profile, highlighting its promise for GI cancer treatment. A first-in-human, phase I clinical trial of AMT-676 in patients with advanced solid tumors is currently underway (NCT06400485).

Indexed as

antibody‐drug conjugatescadherin 17gastrointestinal cancers

Identifiers

PMID42713665
PMCPMC13555363

What Socratic holds

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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 Socratic graph.