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Study of ISM3412 in Participants With Locally Advanced/Metastatic Solid Tumors
NCT06414460 · View on ClinicalTrials.gov ↗
Study Summary
The study has consists of two parts, a dose escalation part (Part 1) and a dose selection optimization part (Part 2). The primary objectives of this study are to evaluate the safety and tolerability of ISM3412 in participants with locally advanced/metastatic solid tumors, and to determine the RP2D of ISM3412.
Conditions Studied
Interventions
- DRUG ISM3412
Study Locations (9)
Colorado
- Sarah Cannon Research Institute at HealthONE — Denver
Connecticut
- Smilow Cancer Hospital at Yale New Haven Breast Center — New Haven
Indiana
- Community Cancer Center North — Indianapolis
Tennessee
- SCRI Oncology Partners — Nashville
Texas
- The University of Texas MD Anderson Cancer Center — Houston
Beijing Municipality
- Cancer Hospital Chinese Academy of Medical Sciences — Beijing
Guangdong
- Sun Yat-sen university cancer center — Guangzhou
Jiangsu
- Jiangsu Provincial People's Hospital — Nanjing
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 80 participants |
| Start Date | 2025-04-25 |
| Est. Completion | 2029-03-31 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06414460
The ClinicalTrials.gov registry entry for NCT06414460 describes a study currently listed as recruiting. It is categorized as Phase 1, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 80 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is InSilico Medicine Hong Kong Limited, which has 3 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Locally Advanced/Metastatic Solid Tumors appearing as the primary indexed condition, and to 1 intervention — of which ISM3412 is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06414460 reports 9 study locations spanning 9 distinct geographic areas — top geographies include Colorado, Connecticut, Indiana. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06414460 about?
NCT06414460 is a clinical study titled "Study of ISM3412 in Participants With Locally Advanced/Metastatic Solid Tumors". The study has consists of two parts, a dose escalation part (Part 1) and a dose selection optimization part (Part 2). The primary objectives of this study are to evaluate the safety and tolerability of ISM3412 in participants with locally advanced/metastatic solid tumors, and to determine the RP2D o...
What is the current status of trial NCT06414460?
This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 80 participants. The study started on 2025-04-25. Estimated completion is 2029-03-31.
What conditions does trial NCT06414460 study?
This clinical trial studies the following conditions: Locally Advanced/Metastatic Solid Tumors. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06414460?
The interventions under investigation include: ISM3412 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06414460?
This trial is sponsored by InSilico Medicine Hong Kong Limited, which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06414460 being conducted?
This trial has 9 study locations across Colorado, Connecticut, Indiana, Tennessee, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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