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.
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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