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Study identifier: NCT06566079 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Study of ISM6331 in Participants With Advanced/Metastatic Malignant Mesothelioma or Other Solid Tumors

Condition: Malignant Mesothelioma · Metastatic Malignant Solid Tumor · Advanced Solid Tumor  ·  Sponsor: InSilico Medicine Hong Kong Limited

PhasePhase 1
Planned participants100
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

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.

Talk to the study team

Qinhan Chen  ·  +86 021-50831718  ·  Insilico-Clinicaltrial@insilico.ai

Always discuss trial participation with your own doctor first.

Locations (10)

Sarah Cannon Research Institute at HealthONEDenver, Colorado, United StatesRecruiting
The University of Chicago Medical Center - Duchossois Center for Advanced MedicineChicago, Illinois, United StatesRecruiting
University Hospitals Cleveland Medical CenterCleveland, Ohio, United StatesRecruiting
University of Pennsylvania - Abramson Cancer CenterPhiladelphia, Pennsylvania, United StatesRecruiting
SCRI Oncology PartnersNashville, Tennessee, United StatesRecruiting
NEXT Oncology - AustinAustin, Texas, United StatesRecruiting
Henan Cancer HospitalZhengzhou, Henan, ChinaRecruiting
Shanghai Pulmonary HospitalShanghai, Shanghai Municipality, ChinaNot Yet Recruiting
Cancer Hospital Chinese Academy of Medical SciencesBeijing, ChinaRecruiting
Sun Yat-Sen University Cancer CenterGuangzhou, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT06566079