Summary
This is a multinational, non-randomized, open-label, Phase 1/2 clinical study to evaluate
the safety, tolerability and anti-tumor efficacy of AZD4205 as monotherapy in patients
with peripheral T cell lymphoma (PTCL), who have relapsed from or are
refractory/intolerant to standard systemic treatment.
Phase 1 part:
Around 20~40 patients will be subsequently enrolled into 2 different dose ascending
cohorts. Additional 10~20 patients may be enrolled to further explore a selected dose
defined by dose escalation cohorts.
Phase 2 part:
After the recommended phase 2 dose (RP2D) is defined, a phase 2 single-arm open-label
pivotal study will be conducted to assess anti-tumor efficacy and safety of AZD4205 at
RP2D in patients with refractory or relapsed PTCL.