drugset / Trial / NCT03444701
A Study of E7130 in Participants With Solid Tumors
Non-randomizedSequentialOpen-labelTreatment
Summary
The primary objective of this study is to evaluate the tolerability and safety profile of E7130 in participants with solid tumors.
Timeline
- Start
- 2018-02-05
- Primary completion
- 2024-12-27
- Completion
- 2024-12-27
Publications
- Matsubara N, Saijo K, Shimizu Y, Okano S, Nakano K, Nishio N, Otsuka T, Kuno H, Miura T, Kubota T, Ikezawa H, Umetsu Y, Ito K, Apfel A, Ye Y, Honma Y. First-In-Human Study: Dose Expansion of E7130 in Urothelial Carcinoma and Squamous Cell Carcinoma of the Head and Neck. Cancer Sci. 2026 May 27. doi: 10.1111/cas.70420. Online ahead of print.
- Doi T, Matsubara N, Naito Y, Kuboki Y, Harano K, Ono M, Urasaki T, Ohmoto A, Kawanai T, Hisai T, Ikezawa H, Shiba S, Ito K, Semba T, Asano O, Takahashi S. First-in-human study of E7130 (a tumor microenvironment-ameliorating microtubule inhibitor) in patients with advanced solid tumors: Primary results of the dose-escalation part. Cancer. 2023 Aug 1;129(15):2348-2359. doi: 10.1002/cncr.34788. Epub 2023 Apr 20.
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | E7130 | Small molecule | 25 ug/m2 | Intravenous |
| Subject | E7130 | Small molecule | 270 ug/m2 | Intravenous |
| Subject | E7130 | Small molecule | 300 ug/m2 | Intravenous |
| Subject | E7130 | Small molecule | 350 ug/m2 | Intravenous |
| Subject | E7130 | Small molecule | 400 ug/m2 | Intravenous |
| Subject | E7130 | Small molecule | 410 ug/m2 | Intravenous |
| Subject | E7130 | Small molecule | 480 ug/m2 | Intravenous |
| Subject | E7130 | Small molecule | 550 ug/m2 | Intravenous |