OncoMatch/Clinical Trials/NCT06824064
Evaluation of RBS2418 in Patients With Advanced, Metastatic, and Progressive Colorectal Cancer
Is NCT06824064 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies RBS2418 for metastatic colorectal cancer.
Treatment: RBS2418 — RBS2418 is a specific immune modulator that works through the inhibition of ectonucleotide pyrophosphatase/phosphodiesterase 1 (ENPP1) and is designed to lead to anti-tumor immunity by protecting endogenous 2'-3'-cyclic guanosine monophosphate-adenosine monophosphate (cGAMP) from hydrolysis and leading to the activation of antigen-presenting cells followed by T cell activation. The hypothesis is that RBS2418 versus placebo will be generally safe, well-tolerated, immunogenic, and will lead to anti-tumor responses in adult subjects for the treatment of advanced, metastatic, and progressive colorectal cancer (CRC).
Check if I qualifyExtracted eligibility criteria
Cancer type
Colorectal Cancer
Disease stage
Required: Stage IV, PROGRESSIVE
Metastatic disease required
advanced, metastatic, progressive CRC
Prior therapy
Must have received: all approved standard of care therapies for metastatic CRC — metastatic
have received, been ineligible for, intolerant to, or declined all approved standard of care (SOC) therapies for metastatic CRC
Cannot have received: any approved anti-cancer therapy including chemotherapy, targeted small molecule therapy, systemic immunotherapy, or radiation therapy
Exception: palliative radiotherapy for bone metastases or soft tissue lesions completed >7 days prior; hormone-replacement therapy or oral contraceptives; subjects with Grade 2 neuropathy or Grade 2 alopecia
Any approved anti-cancer therapy including chemotherapy, targeted small molecule therapy, systemic immunotherapy, or radiation therapy within 2 weeks prior to the first dose of study treatment; or if subject has not recovered (i.e., ≤ to Grade 1 or returned to baseline level) from AEs due to a previously administered agent; the following exceptions are allowed: * Palliative radiotherapy for bone metastases or soft tissue lesions should be completed >7 days prior to the first dose of study treatment. * Hormone-replacement therapy or oral contraceptives. * Subjects with Grade 2 neuropathy or Grade 2 alopecia.
Structured fields extracted by AI. May contain errors — verify against the official protocol.
US trial sites
- Community Clinical Trials · Kingwood, Texas
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