Condition: Malignant Mesothelioma · Metastatic Malignant Solid Tumor · Advanced Solid Tumor · Sponsor: InSilico Medicine Hong Kong Limited
This is a Phase 1, open-label, multicenter, FIH study to evaluate the safety, tolerability, recommended Phase 2 dose (RP2D), PK/PD, and preliminary anti-tumor activity of ISM6331 in participants with advanced or metastatic malignant mesothelioma or other solid tumors. The study consists of two parts, a dose escalation part (Part 1) and a dose selection optimization part (Part 2).
This description comes directly from the study's public registry record.
Qinhan Chen · +86 021-50831718 · Insilico-Clinicaltrial@insilico.ai
Always discuss trial participation with your own doctor first.
| Sarah Cannon Research Institute at HealthONE | Denver, Colorado, United States | Recruiting |
| The University of Chicago Medical Center - Duchossois Center for Advanced Medicine | Chicago, Illinois, United States | Recruiting |
| University Hospitals Cleveland Medical Center | Cleveland, Ohio, United States | Recruiting |
| University of Pennsylvania - Abramson Cancer Center | Philadelphia, Pennsylvania, United States | Recruiting |
| SCRI Oncology Partners | Nashville, Tennessee, United States | Recruiting |
| NEXT Oncology - Austin | Austin, Texas, United States | Recruiting |
| Henan Cancer Hospital | Zhengzhou, Henan, China | Recruiting |
| Shanghai Pulmonary Hospital | Shanghai, Shanghai Municipality, China | Not Yet Recruiting |
| Cancer Hospital Chinese Academy of Medical Sciences | Beijing, China | Recruiting |
| Sun Yat-Sen University Cancer Center | Guangzhou, China | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06566079