Celator joins leukemia society for phase II trial of CPX-351

Publication
Article
Oncology NEWS InternationalOncology NEWS International Vol 18 No 2
Volume 18
Issue 2

Celator Pharmaceuticals and the Leukemia & Lymphoma Society have partnered for the phase II development of CPX-351 (cytarabine:daunorubicin), a liposome injection for treatment of adults with acute myeloid leukemia.

Celator Pharmaceuticals and the Leukemia & Lymphoma Society have partnered for the phase II development of CPX-351 (cytarabine:daunorubicin), a liposome injection for treatment of adults with acute myeloid leukemia.

Through the partnership, the society will provide $3.7 million to support the multicenter, randomized, open-label trial of CPX-351 compared with intensive salvage therapy in adult patients (≤ 60 years of age) with AML in first relapse. Celator expects to start patient enrollment in this study in the first quarter of 2009 in the U.S. and Canada. CPX-351 has also been granted orphan drug status by the FDA for the treatment of AML.

The collaboration is part of the society’s Therapy Acceleration Program, which supports private sector and academic-based projects that advance investigational therapies.

Newsletter

Stay up to date on recent advances in the multidisciplinary approach to cancer.

Recent Videos
For patients with locally advanced head and neck cancers, the current standard of care for curative therapy has a cure rate of less than 50%.
According to Maurie Markman, MD, patient-reported outcomes pertain to more relevant questions surrounding the impact of therapy for patients.
CancerNetwork® spoke with Neha Mehta-Shah, MD, MSCI, about the clinical landscape for patients undergoing treatment for rare lymphomas.
Related Content