Condition: Neoplasms · Glioblastoma, Adult · Small Cell Lung Carcinoma (SCLC) · Sponsor: Chipscreen Biosciences, Ltd.
This trial is a single-arm, open-label, first-in-human study of CS231295, comprising two phases: dose escalation (including single-dose and multiple-dose) and cohort expansion. The Dose-Limiting Toxicity (DLT) observation period includes 6 days for single-dose and the first cycle (28 days) for multiple-dose. The overall study consists of screening period, treatment period, and follow-up period. The primary objectives of this study are to evaluate the safety, tolerability and pharmacokinetic (PK) characteristics of CS231295 in patients with advanced solid tumors, and to recommended Phase 2 dose(s) (RP2D) of CS231295 in appropriate tumor(s).
This description comes directly from the study's public registry record.
Xinhang Wang · +86 0755-36993500 · xinhwang@chipscreen.com
Always discuss trial participation with your own doctor first.
| Beijing Tiantan Hospital, Capital Medical University | Beijing, Beijing Municipality, China | Not Yet Recruiting |
| Jilin Cancer Hospital | Changchun, Jilin, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06902350