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A Study of IBI363 in Subjects with Advanced Solid Malignancies
NCT06281678 · View on ClinicalTrials.gov ↗
Study Summary
This is a Phase 2, open-label, multicenter study designed to evaluate the efficacy, safety and tolerability of IBI363 (study drug) in subjects with advanced, refractory solid malignancies.
Conditions Studied
Interventions
- DRUG IBI363
Study Locations (9)
Florida
- Ocala Oncology Center — Ocala
- BRCR Medical Center — Plantation
Michigan
- Michigan Hematology & Oncology Consultants - MedOnc Dearborn — Dearborn
- Michigan Hematology & Oncology Consultants - MedOnc Troy — Troy
Texas
- MD Anderson Cancer Center-University of Texas — Houston
- Oncology Consultants P.A. — Houston
California
- University of California, San Francisco (UCSF) — San Francisco
Kansas
- University of Kansas Medical Center (KUMC) — Fairway
Washington
- Fred Hutchinson Cancer Center — Seattle
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 178 participants |
| Start Date | 2024-04-08 |
| Est. Completion | 2026-12-31 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06281678
The ClinicalTrials.gov registry entry for NCT06281678 describes a study currently listed as recruiting. It is categorized as Phase 2, 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 178 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Innovent Biologics (Suzhou) Co., 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 4 conditions, with Colorectal Cancer appearing as the primary indexed condition, and to 1 intervention — of which IBI363 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: NCT06281678 reports 9 study locations spanning 6 distinct geographic areas — top geographies include Florida, Michigan, Texas. 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 NCT06281678 about?
NCT06281678 is a clinical study titled "A Study of IBI363 in Subjects with Advanced Solid Malignancies". This is a Phase 2, open-label, multicenter study designed to evaluate the efficacy, safety and tolerability of IBI363 (study drug) in subjects with advanced, refractory solid malignancies.
What is the current status of trial NCT06281678?
This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 178 participants. The study started on 2024-04-08. Estimated completion is 2026-12-31.
What conditions does trial NCT06281678 study?
This clinical trial studies the following conditions: Colorectal Cancer, Melanoma, Non-small Cell Lung Cancer, Renal Cell Cancer. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06281678?
The interventions under investigation include: IBI363 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06281678?
This trial is sponsored by Innovent Biologics (Suzhou) Co., 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 NCT06281678 being conducted?
This trial has 9 study locations across California, Florida, Kansas, Michigan, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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