First-in-human Trial of STC-1010, an Immunotherapy, in Patients With Unresectable Locally Advanced or Metastatic Colorectal Cancer
Condition(s) studied
Investigational drug(s) / intervention(s)
STC-1010 + IS regimen + SOC therapy: STC-1010 administered with immunostimulants (IS) in low-dose (cyclophosphamide and GM-CSF) and standard of care (SOC) therapy (mFOLFOX6 with or without bevacizumab)
Study summary
This is a phase I/IIA, first-in-human (FIH), two-part, open-label, multicenter study to characterize the safety, tolerability profile, and clinical efficacy of STC-1010 associated with GM-CSF and cyclophosphamide immunostimulant (IS) regimen administered with standard of care (SOC) therapy (mFOLFOX6 with or without bevacizumab) to participants with unresectable locally advanced (stage IIIC, T4b) or unresectable metastatic (stage IV) colorectal cancer (CRC).
The trial will be conducted in two parts:
* A Phase I consisting of a dose escalation part and small expansion part to determine the maximum tolerated dose (MTD), recommended Phase II dose (RP2D) and safety profile of the STC-1010 + IS regimen administered with SOC therapy. Approximately 21 to 33 participants will be included in this phase in Europe.
* A Phase IIA consisting of the expansion stage of the study which will further evaluate the clinical efficacy and safety of STC-1010 on a larger number of participants treated at the identified RP2D. Approximately 57 to 60 participants will be enrolled in total in 2 different arms. Multi-site recruitment will take place in Europe and in the US.
Eligibility
Primary outcome measure(s)
- Phase 1: To determine overall safety profile, recommended Phase 2 dose (RP2D) and maximum tolerated dose (MTD) — 28 days
Endpoint/Outcome Measures: Incidence, severity, and relationship of Treatment Emergent Adverse Events (TEAEs), Serious Adverse Events (SAEs), Dose-Limiting Toxicities (DLT) (in dose escalation part), AEs leading to treatment discontinuation; and clinically significant findings on clinical laboratory tests, vital signs, electrocardiograms (ECGs), and physical examinations, using the Common Terminology Criteria for Adverse Events (CTCAE Version 5). - Phase 2A: To determine the clinical efficacy by Progression Free Survival (PFS) rate — 12 months
Progression Free Survival (PFS) rate at 12 months from STC-1010 + IS regimen initiation, defined as the proportion of participants alive and without progression (i.e., participants with complete response \[CR\], partial response \[PR\] or stable disease \[SD\]) at 12 months according to RECIST 1.1
Trial sites (9)
| Facility | City | Region | Status |
|---|---|---|---|
| Johns Hopkins | Baltimore | Maryland | Not Yet Recruiting |
| Institut Jules Bordet | Brussels | Belgium | Recruiting |
| Institut Bergonié | Bordeaux | France | Recruiting |
| Centre Georges François Leclerc (CGFL) | Dijon | France | Recruiting |
| Centre Léon Bérard (CLB) | Lyon | France | Recruiting |
| Hospices Civils de Lyon (HCL) | Lyon | France | Recruiting |
| Institut du Cancer de Montpellier (ICM) | Montpellier | France | Recruiting |
| Centre Hospitalier Universitaire de Poitiers (CHU) | Poitiers | France | Not Yet Recruiting |
| Institut Gustave Roussy (IGR) | Villejuif | France | Recruiting |
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT06934538 on ClinicalTrials.gov ↗ ← All trials in the USA