Drug: Voreloxin Abstract No. 5002 Indication: ovarian cancer Clinical Trial: Final results of a phase II study of voreloxin in women with platinum-resistant ovarian cancer. Presentation Time: Monday, June 7. Oral session. Notes: Final response rate across three different dosages of Voreloxin was 11% with a median progression-free survival of 84 days.
Sunesis will also be presenting final phase II data from a study of voreloxin in patients with acute myeloid leukemia.
Final results of a phase II pharmacokinetic/pharmacodynamic (PK/PD) study of combination voreloxin and cytarabine in patients with relapsed or refractory acute myeloid leukemia. http://abstract.asco.org/AbstView_74_49274.html
Voreloxin single-agent treatment of older patients (60 years or older) with previously untreated acute myeloid leukemia: Final results from a phase II study with three schedules http://abstract.asco.org/AbstView_74_49315.html
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