Phase 1 Pancreatic Cancer Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- You have been diagnosed with a specific type of advanced cancer (non-small cell lung cancer, pancreatic cancer, colorectal cancer, or another solid tumor) that has spread or cannot be surgically removed, and your tumor has been confirmed by a lab test to have a specific gene change called a KRAS G12A, G12C, G12D, G12S, or G12V mutation
- Your cancer can be measured on scans using a standard measurement system called RECIST v1.1
- You are generally able to carry out daily activities with little or no limitation (confirm with trial site for exact fitness level required)
- Doctors expect your life expectancy to be more than 24 weeks (about 6 months)
- Your liver, kidneys, blood, and other organs are functioning well enough as shown by lab tests (confirm with trial site for specific levels required)
Who may not be able to join:
- You have been diagnosed with another cancer within the last 2 years (confirm with trial site for specific exceptions listed in the protocol)
- You have cancer that has spread to the brain and has not yet been treated
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Phone: (650) 405-4770
Australian sites
03-8559-5000
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
1 site(s) in Australia. Confirm current status and contact details directly with the trial site.
Primary endpoints
Incidence and severity of treatment emergent adverse events (TEAEs), serious adverse events (SAEs), and dose-limiting toxicities (DLTs); Determine recommended dose of BBO-11818 in combination with pembrolizumab ± cis/carboplatin + pemetrexed, cetuximab ± mFOLFOX6, BBO-10203 + mFOLFOX6, BBO-10203 + cetuximab, cetuximab, mFOLFIRINOX, gemcitabine + nab-paclitaxel, or BBO-10203
Can't join this trial?
Data last synced from ClinicalTrials.gov: 22 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.