ODM-207 in Patients With Advance Solid Tumours (NCT03035591) | Clinical Trial Compass
CompletedPhase 1/2
ODM-207 in Patients With Advance Solid Tumours
Finland36 participantsStarted 2016-12-22
Plain-language summary
This is a first-in-man study to assess the safety and tolerability and to characterise the pharmacokinetics of ODM-207.
Who can participate
Age range18 Years
SexALL
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Inclusion Criteria:
* Patients with histologically or cytologically confirmed locally advanced or metastatic cancer for which no effective standard therapy exists or are refractory or resistant to conventional therapy
* Life expectancy \>12 weeks
* Patient may have either measurable or non-measurable disease, but must have disease that can be evaluated for improvement of progression
* ECOG performance status of 0 to 1
Exclusion Criteria:
* History of bleeding disorder or significant bleeding episode within 6 months prior to study treatment
* Subjects receiving anticoagulants or medications that durably inhibit platelet function (7-day wash-out prior to study treatment)
* History of or current leptomeningeal or brain metastasis or spinal cord compression.