*Mesoblast's Phase 2 trial of allogeneic, or "off-the-shelf", Mesenchymal
    Precursor Cells (MPCs) injected into damaged intervertebral discs has now
    completed six-month follow-up for all 100 patients enrolled
  *A pre-specified interim analysis of Phase 2 trial results was performed
    when 50% of patients completed six months of follow-up. This analysis
    demonstrated that a single low-dose MPC injection resulted in
    significantly greater reduction in low back pain and improvement in
    function than was seen in patients receiving the hyaluronic acid carrier
    alone, with no cell-related safety issues
  *In the interim analysis, 71% of patients who received a low dose MPC
    injection met the pre-specified treatment success criteria at 6 months
    compared with only 20% and 30% of the patients in the two control arms who
    received hyaluronic acid and saline
  *Full trial results expected in Q3 2013
  *Confirmation of interim results would support progression to Phase 3 for
    MPC treatment of chronic discogenic low back pain.

NEW YORK and MELBOURNE, Australia, April 22, 2013 (GLOBE NEWSWIRE) --
Regenerative medicine company Mesoblast Limited (ASX:MSB) (USOTC:MBLTY) today
announced that all 100 patients in its Phase 2 clinical trial of its
proprietary Mesenchymal Precursor Cells (MPCs) for intervertebral disc repair
had completed six months of follow-up, the endpoint at which data will be
evaluated for progression to Phase 3.

Additionally, Mesoblast announced that it had completed the pre-specified
interim analysis which was performed when 50% of the patients had completed
their six month follow-up visits. The analysis showed a positive outcome, with
a single low-dose injection of MPCs causing a significantly greater reduction
in low back pain, significantly greater improvement in function, and
significantly greater treatment success compared with patients who received
hyaluronic acid carrier alone, with no cell-related serious adverse events.

Over 6 million patients in the United States alone are currently dealing with
chronic back pain that has persisted for at least three months. The CDC's
National Center for Health Statistics reported in 2010 that low back pain was
the leading cause of pain, affecting 28% of American adults. The United States
lifetime prevalence of low back pain is estimated to be at least 60-84%. Total
costs of low back pain are estimated to be between $100 billion and $200
billion annually, two thirds of which are due to decreased wages and

In Mesoblast's Phase 2 clinical trial, 100 patients were enrolled across 13
sites in the United States and Australia. Patients were randomized to receive
direct intra-disc injection of saline (n= 20), hyaluronic acid (HA, n=20), 6
million MPCs in hyaluronic acid carrier (6M, n=30) or 18 million MPCs in
hyaluronic acid carrier (18M, n=30). Patients underwent the outpatient
injection procedure for a single painful degenerated lumbar level and were
evaluated for safety and efficacy at 30 days, 3 months and 6 months. Patients
will continue to be followed for a total of 36 months to evaluate long-term
treatment effects.

The pre-specified interim analysis was conducted when 50% of the enrolled
patients had completed 6 months follow up. At 6 months, patients in all four
treatment arms demonstrated substantial improvement in pain and function
compared to baseline. Patients injected with 6M MPCs + HA demonstrated
significantly greater improvement in back pain and function relative to
baseline when compared with patients receiving HA alone (mean reduction in
back pain 69% vs 38%, p=0.013, and mean improvement in function 51% vs 19%,
p=0.038). Similar trends were seen comparing 6M MPC-treated patients against
saline-treated patients. MRI status of disc morphology remained unchanged at 6
months relative to baseline in all groups.

Overall treatment success was defined as the pre-specified composite requiring
a patient to meet all of the following criteria: clinically significant levels
of improvement in back pain and function at 6 months compared to baseline,
maintenance or improvement in neurological status from baseline, maintenance
of disc morphology compared to baseline as evaluated by MRI, and no serious
adverse event or secondary intervention. In the interim analysis, 71% of
patients treated with 6M MPC+HA were determined to be a treatment success
compared with 20% in the HA alone group (p=0.036) and 30% in the saline
injected group (p=0.095). Additionally, the 6M MPC group showed significantly
higher overall treatment success rates than the group receiving 18M MPCs, due
to both lower efficacy and higher incidence of adverse events with the higher

"We are pleased that the interim results of this important study have
identified a low MPC dose that appears to be safe and effective for inducing
sustained improvement in low back pain and function," said Mesoblast Chief
Executive Professor Silviu Itescu.

The complete results of the Phase 2 trial will be presented during the third
quarter 2013. If the full results are consistent with the interim results,
Mesoblast plans to commence a Phase 3 trial of a single MPC dose injected into
damaged intervertebral discs to treat chronic low back pain.

It is important to note that while interim results are often indicative, they
should not be taken as conclusive of the final trial results. The Company does
not at present have the full analyzed data from all 100 patients in the trial,
and there is no guarantee the full trial results will match the interim data.

Mesoblast Limited

Mesoblast Limited is a world leader in the development of biologic products
for the broad field of regenerative medicine. Mesoblast's patented Mesenchymal
Precursor Cell (MPC) technology is being developed for an extensive range of
major clinical diseases, including inflammatory and immunologic conditions of
the joints and lungs, diabetes and kidney disease, orthopedic spine
conditions, and cardiovascular disorders.

CONTACT: Julie Meldrum
         Global Head of Corporate Communications
         Mesoblast Limited
         T: + 61 (0) 3 9639 6036
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