Active Biotech Completes Patient Enrollment to ANYARA Phase III Clinical Trial


Active Biotech (NASDAQ OMX NORDIC: ACTI) today announced that patient
enrollment to the Phase III clinical trial for ANYARA, a novel
compound for the treatment of renal cell cancer, is completed after
enrollment of over 500 patients into the study.

This pivotal Phase  III study  evaluates the efficacy  and safety  of
ANYARA   in    combination   with    interferon-alfa   compared    to
interferon-alfa alone, in patients  with advanced renal cell  cancer.
The primary clinical efficacy parameter is overall survival.

Final survival data for ANYARA will be analyzed after 384 events  and
the current estimate is  that these will be  presented by the end  of
2010/beginning of 2011.


Lund 1 June 2009
Active Biotech AB (publ)

Tomas Leanderson
President & CEO


About ANYARA
ANYARA is a TTS (Tumor  Targeting Superantigens) compound that  makes
the treatment of cancer tumor-specific. The development of ANYARA  is
mainly focused on renal  cell cancer. Positive  data was reported  in
connection with  the  interim  analysis  in  Phase  II/III  and  from
clinical Phase  I  trials  in  lung cancer,  renal  cell  cancer  and
pancreatic cancer. The  median survival of  26.2 months observed  for
patients with advanced renal cancer and treated with ANYARA is  twice
the expected length.  ANYARA has been  granted orphan-drug status  by
the EMEA for the indication renal cancer. Information concerning  the
ongoing clinical  trial  is available  at  www.activebiotech.com  and
www.clinicaltrials.gov.

About Active Biotech
Active Biotech  AB  (NASDAQ  OMX NORDIC:  ACTI)  is  a  biotechnology
company with focus  on autoimmune/inflammatory  diseases and  cancer.
Projects in  pivotal phase  are  laquinimod, an  orally  administered
small  molecule  with  unique  immunomodulatory  properties  for  the
treatment of multiple sclerosis, as well as ANYARA for use in  cancer
targeted therapy, primarily of renal cancer. Further key projects  in
clinical development comprise the three orally administered compounds
TASQ for prostate cancer, 57-57 for SLE and RhuDex(TM) for RA. Please
visit www.activebiotech.com for more information.

Active Biotech AB
PO Box 724, SE-220 07 Lund
Sweden
Tel: +46 (0)46-19 20 00
Fax: +46 (0)46-19 11 00

Active Biotech is required under  the Securities Markets Act to  make
the information in  this press  release public.  The information  was
submitted for publication at 08:30 am CET on June 1, 2009.