Presentation highlights include:
-- A Phase I Study Evaluating the Safety, Pharmacokinetics, and Efficacy
of ABT-263 in Subjects With Refractory or Relapsed Lymphoid
Malignancies
-- Reduction in Platelet Counts as a Mechanistic Biomarker and Guide for
Adaptive Dose-escalation in Phase I Studies of the Bcl-2 Family
Inhibitor ABT-263
-- Dynamic Contrast Enhanced MRI (DCE MRI) for Assessment of Effects of
Anti-Angiogenic Therapy: Comparison of the Transfer Constant (Ktrans)
to Blood Flow and Permeability Derived by a Distributed Parameter
Model
-- Relationship of Dose of ABT-869 on Biomarkers of Angiogenesis and
Their Correlation With Pharmacodynamic (PD) Outcome
Study Background and Results
ABT-263
Thirty patients with refractory or relapsed lymphoid malignancies have
been enrolled in an ongoing Phase I study evaluating safety,
pharmacokinetics and efficacy. Subjects received ABT-263 orally once daily
for 14 consecutive days followed by seven days off drug in each cycle of
therapy. Results showed that ABT-263 had an acceptable side-effect profile
at the seven-dose (10, 20, 40, 80, 160, 225 and 315 mg) cohort levels and
showed evidence of anti-tumor activity. Researchers observed 99 percent and
36 percent tumor reduction in two patients with bulky chronic lymphocytic
leukemia (CLL). Another patient with bulky CLL/small lymphocytic lymphoma
(SLL) experienced a 75 percent reduction and a patient with follicular
lymphom
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