Advanced Solid Malignancies Clinical Trial
Official title:
A Phase I Clinical Trial to Determine the Maximum Tolerated Dose and to Assess the Safety and Pharmacokinetic Profile of OratecanTM in Patients With Advanced Solid Cancer(Q1DX5/W for 3W)
The main objective of this study is to determine the maximum tolerated dose (MTD) of OratecanTM. Eligible subjects of this study are patients with histologically or cytologically confirmed malignant solid tumor refractory to standard therapy or for which no established therapy exists at the time of study participation.
Besides the main objective, there are 3 other objectives as follows.
1. To determine dose-limiting toxicity (DLT) of OratecanTM
2. To characterize the pharmacokinetics of HM30181A, irinotecan and its metabolites (SN-38
and SN-38G) following oral administration of OratecanTM
3. To evaluate anticancer activity of OratecanTM in patients with advanced solid
malignancies Groups of 3 patients per cohort or dose level will be treated with
escalating doses of irinotecan in combination with a fixed 60mg dose of HM30181A.
If 0/3 patients at any dose level experience a DLT, the dose of irinotecan will be escalated
by 10 mg/m2 in the next dose level. If 1/3 patients at any dose level experience a DLT, the
cohort will be expanded by 3 additional patients to 6 patients. If no additional patients
develop DLT, the dose of irinotecan will again be escalated in the next cohort of 3 patients.
If 2/3 or 2/6 patients develop DLT, then dose escalation will cease, and the previous dose
will be declared the MTD.
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