Abstract CT092: A Phase 1a/1b, first-in-human study of an ADC targeting ADAM9 (DB-1317) in participants with selected advanced or metastatic solid tumors

Abstract Background: A disintegrin and a metalloprotease 9 (ADAM9) is highly expressed in several cancer types and its expression level correlates with a suppressive tumor microenvironment, metastasis, and poor prognosis, making it a promising therapeutic target. DB-1317 is an antibody-drug conjugate (ADC) comprised of an anti-ADAM9 antibody linked to a topoisomerase I inhibitor via a cleavable tetrapeptide linker, with a drug-to-antibody ratio of approximately 8. Preclinical studies demonstrated that DB-1317 induced ADAM9-dependent cytotoxicity, exhibited both by-stander killing effect and antibody-dependent cellular cytotoxicity. In addition, DB-1317 is well-tolerated at a dose of up to 80 mg/kg in cynomolgus monkeys. These findings warrant clinical development of DB-1317 (Shengchao Lin, AACR 2025). Methods: The first-in-human phase 1a/1b study (NCT07141706) aims to assess the safety, tolerability, pharmacokinetics, and preliminary anti-tumor activities of DB-1317 in participants with selected unresectable advanced/metastatic solid tumors, without mandatory requirement for a minimum ADAM9 expression level. The study is planned to enroll approximately 223 participants from the United States, Australia, and China (up to 63 in phase 1a and approximately 160 in phase 1b).In phase 1a (dose escalation part), participants who have progressed on/after or are intolerant to standard treatments for advanced/unresectable or metastatic selected solid tumors will be enrolled to identify the maximum tolerated dose or maximum administered dose of DB-1317. Selected solid tumors include gastric cancer (GC), colorectal cancer (CRC), pancreatic ductal adenocarcinoma (PDAC), cholangiocarcinoma, non-small cell lung cancer, and castrate-resistant prostate cancer. Approximately five ascending dose levels of DB-1317 (accelerated titration design for the first dose level and a BOIN design for subsequent dose levels) will be administered by intravenous infusion. The dose-limiting toxicities (DLT) will be assessed. When a dose level is confirmed to be safe by the Safety Monitoring Committee (SMC), backfill participants may be enrolled to further evaluate DB-1317. Phase 1b (dose expansion part) will include one randomized expansion cohort in GC and two single-arm expansion cohorts in CRC and PDAC, if preliminary anti-tumor activities in these tumor types are observed in phase 1a part. Dose levels used in phase 1b part will be determined by sponsor and SMC based on phase 1a data. As of Dec 24, 2025, 7 participants have been enrolled in Australia and the United States. Citation Format: Charlotte Lemech, Alexander Spira, David Sommerhalder, Siqing Fu, Feijiao Ge, Hua Mu, Yang Yang, Yang Qiu, Jiajia Chen, Rong Shi, Zhongyuan Zhu, Ruihua Xu. A Phase 1a/1b, first-in-human study of an ADC targeting ADAM9 (DB-1317) in participants with selected advanced or metastatic solid tumors [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 2 (Late-Breaking, Clinical Trial, and Invited Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(8_Suppl):Abstract nr CT092.

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Journal
Cancer Research
Published
2026-04-17
DOI
https://doi.org/10.1158/1538-7445.am2026-ct092
Primary Topic
HER2/EGFR in Cancer Research
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article

Abstract CT092: A Phase 1a/1b, first-in-human study of an ADC targeting ADAM9 (DB-1317) in participants with selected advanced or metastatic solid tumors

F J Ge, Charlotte Lemech, Ruihua Xu, David Sommerhalder et al.
Cancer Research
HER2/EGFR in Cancer Research
article

Abstract CT092: A Phase 1a/1b, first-in-human study of an ADC targeting ADAM9 (DB-1317) in participants with selected advanced or metastatic solid tumors

F J Ge, Charlotte Lemech, Ruihua Xu, David Sommerhalder, Hua Mu, Yang Qiu, Siqing Fu, Zhongyuan Zhu, Jiajia Chen, Rong Shi, Alexander Spira, Yang Yang
article en

Abstract

Abstract Background: A disintegrin and a metalloprotease 9 (ADAM9) is highly expressed in several cancer types and its expression level correlates with a suppressive tumor microenvironment, metastasis, and poor prognosis, making it a promising therapeutic target. DB-1317 is an antibody-drug conjugate (ADC) comprised of an anti-ADAM9 antibody linked to a topoisomerase I inhibitor via a cleavable tetrapeptide linker, with a drug-to-antibody ratio of approximately 8. Preclinical studies demonstrated that DB-1317 induced ADAM9-dependent cytotoxicity, exhibited both by-stander killing effect and antibody-dependent cellular cytotoxicity. In addition, DB-1317 is well-tolerated at a dose of up to 80 mg/kg in cynomolgus monkeys. These findings warrant clinical development of DB-1317 (Shengchao Lin, AACR 2025). Methods: The first-in-human phase 1a/1b study (NCT07141706) aims to assess the safety, tolerability, pharmacokinetics, and preliminary anti-tumor activities of DB-1317 in participants with selected unresectable advanced/metastatic solid tumors, without mandatory requirement for a minimum ADAM9 expression level. The study is planned to enroll approximately 223 participants from the United States, Australia, and China (up to 63 in phase 1a and approximately 160 in phase 1b).In phase 1a (dose escalation part), participants who have progressed on/after or are intolerant to standard treatments for advanced/unresectable or metastatic selected solid tumors will be enrolled to identify the maximum tolerated dose or maximum administered dose of DB-1317. Selected solid tumors include gastric cancer (GC), colorectal cancer (CRC), pancreatic ductal adenocarcinoma (PDAC), cholangiocarcinoma, non-small cell lung cancer, and castrate-resistant prostate cancer. Approximately five ascending dose levels of DB-1317 (accelerated titration design for the first dose level and a BOIN design for subsequent dose levels) will be administered by intravenous infusion. The dose-limiting toxicities (DLT) will be assessed. When a dose level is confirmed to be safe by the Safety Monitoring Committee (SMC), backfill participants may be enrolled to further evaluate DB-1317. Phase 1b (dose expansion part) will include one randomized expansion cohort in GC and two single-arm expansion cohorts in CRC and PDAC, if preliminary anti-tumor activities in these tumor types are observed in phase 1a part. Dose levels used in phase 1b part will be determined by sponsor and SMC based on phase 1a data. As of Dec 24, 2025, 7 participants have been enrolled in Australia and the United States. Citation Format: Charlotte Lemech, Alexander Spira, David Sommerhalder, Siqing Fu, Feijiao Ge, Hua Mu, Yang Yang, Yang Qiu, Jiajia Chen, Rong Shi, Zhongyuan Zhu, Ruihua Xu. A Phase 1a/1b, first-in-human study of an ADC targeting ADAM9 (DB-1317) in participants with selected advanced or metastatic solid tumors [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2026; Part 2 (Late-Breaking, Clinical Trial, and Invited Abstracts); 2026 Apr 17-22; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2026;86(8_Suppl):Abstract nr CT092.

Cancer ResearchVol. 86(8_Supplement)
The University of Texas MD Anderson Cancer Center (US), Sun Yat-sen University (CN), Texas Oncology (US), Urology of Virginia (US), BioScientia (Poland) (PL), Sun Yat-sen University Cancer Center (CN), Cell Biologics (United States) (US)
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Openalex Percentile: Top 16%
HER2/EGFR in Cancer Research
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