The main purpose of this study is to establish the safety and the recommended dose of TRK-950 in combination with FOLFIRI, Gemcitabine / Cisplatin, Gemcitabine / Carboplatin, Ramucirumab / Paclitaxel, PD1 inhibitors (Nivolumab or Pembrolizumab), and Imiquimod Cream, Bevacizumab, Gemcitabine / Carboplatin / Bevacizumab, Pegylated liposomal doxorubicin (PLD), Carboplatin / PLD / Bevacizumab and Paclitaxel for selected advanced solid tumors.
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
Frequency of patients experiencing treatment emergent adverse events as assessed by CTCAE v5.0
Timeframe: through study completion, an average of 1 year
Frequency of patients experiencing adverse events of special interest (AESIs)
Timeframe: through study completion, an average of 1 year
Blood pressure
Timeframe: through study completion, an average of 1 year
Heart rate
Timeframe: through study completion, an average of 1 year
Respiratory rate
Timeframe: through study completion, an average of 1 year
Temperature
Timeframe: through study completion, an average of 1 year
Weight
Timeframe: through study completion, an average of 1 year
Height
Timeframe: through study completion, an average of 1 year
Performance status using Karnofsky performance status criteria
Timeframe: through study completion, an average of 1 year
QTc interval determined from 12-lead Electrocardiogram
Timeframe: through study completion, an average of 1 year
QRS interval determined from 12-lead Electrocardiogram
Timeframe: through study completion, an average of 1 year
Frequency of patients with laboratory abnormalities (Complete Blood Count, Coagulation, Urinalysis and Serum Chemistry)
Timeframe: through study completion, an average of 1 year