AS1413 (amonafide L-malate, formerly XanafideŽ)


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AS1413 is a DNA intercalator that induces apoptotic signalling by blocking TopoII binding to DNA. Unlike classical TopoII inhibitors, a distinctive feature of AS1413 is its ability to evade PgP and related transporters responsible for multi-drug resistance. AS1413 is currently in phase III development in secondary AML.

Secondary AML (acute myeloid leukaemia)

AML is divided into two major categories, de-novo and secondary. AML is classified as secondary AML if it occurs as a result of a prior haematological disease or treatment with chemotherapy or radiation therapy or a combination of the two causes. In a phase II trial, treatment with AS1413 plus cytarabine resulted in a complete response rate of 38.6%, with an additional 3.4% showing CRi (complete response without recovery of blood cell count). This compares with CR rates of around 25% seen with standard treatment in similar AML patients enrolled in two large American studies. AS1413 is now in a phase III registration trial called ACCEDE. The ACCEDE trial compares AS1413 plus cytarabine with daunorubicin plus cytarabine in 450 patients.

Latest presentation


  • Pgp impacts on CR rates in AML, poster presentation at ASCO, Chicago 2010 (PDF, 191 KB, opens a new browser window)
  • sAML: a valid subgrouping in patients treated with AS1413 regimen (PDF, 184 KB, opens a new browser window)
  • AS1413 AML study rationale and design, poster presentation at ASCO, Chicago 2010(PDF, 256 KB, opens a new browser window)

Clinical presentations


  • AS1413 is equally effective in older and younger patients with sAML, poster presentation at ASH, New Orleans 2009 (PDF, 394 KB, opens a new browser window)
  • Monosomal karyotype is predictive of response in sAML, poster presentation at ASH, New Orleans 2009 (PDF, 175 KB, opens a new browser window)
  • Durable Responses in Poor-Risk AML poster presentation at ASH San Francisco 2008 (PDF, 205 KB, opens a new browser window)
  • AS1413 clinical data paper Review in Haematological Cancers (PDF, 508 KB, opens a new browser window)
  • AML clinical and preclinical summary at EHA, Copenhagen, June 2008 (PDF, 315 KB, opens a new browser window)
  • AML poster presentation at ASCO Chicago 2008 (PDF, 113 KB, opens a new browser window)

Non-clinical presentations


  • AS1413 is distinct from daunorubicin and etoposide, poster presentation at AACR, Washington 2010 (PDF, 2.2 MB, opens a new browser window)
  • AS1413 phase II efflux patient blast cell data poster presentation at EHA, Berlin 2009 (PDF, 141 KB, opens a new browser window)
  • AS1413 is a unique TopoII inhibitor; poster presentation at AACR, Denver 2009 (PDF, 608 KB, opens a new browser window)
  • AML poster presentation at AACR San Diego 2008 (PDF, 117 KB, opens a new browser window)