Acorda Initiates Study on rHIgM22 - Analyst Blog
26 4월 2013 - 2:30AM
Zacks
Acorda Therapeutics, Inc. (ACOR) and Mayo
Clinic announced the enrollment of the first patient in a phase I
safety study of rHIgM22. rHIgM22, a remyelinating monoclonal
antibody, is being evaluated for the treatment of multiple
sclerosis (MS). The study will evaluate the safety, tolerability
and efficacy of rHIgM22.
Acorda already has a presence in the MS market in the form of
Ampyra, which is approved for the improvement of walking in
patients suffering from MS. Acorda is currently working on
expanding Amypra’s label into additional indications.
The company recently presented encouraging data on Ampyra from
two phase II proof-of-concept studies for cerebral palsy and
post-stroke deficit. The company plans to discuss further
development of Ampyra for the post-stroke deficit indication with
the FDA.
Acorda has an agreement with Biogen Idec Inc.
(BIIB) for marketing Ampyra outside the US under the trade name
Fampyra. Fampyra is approved in the EU, Canada, Australia, Israel
and New Zealand.
According to Acorda, about 400,000 people in the US suffer from
MS. In addition, every year approximately 10,000 patients are
diagnosed. Moreover, in the EU, approximately 600,000 people have
MS.
We remind investors that companies like Biogen and
Novartis AG (NVS) have a strong presence in the MS
market. Biogen has MS products like Tysabri and Avonex in its
portfolio. The company recently gained approval for Tecfidera, its
oral MS treatment. Meanwhile, Novartis’ Gilenya is used for the
treatment of relapsing forms of MS.
Presently, Acorda carries a Zacks Rank #3 (Hold). Comparatively,
other biopharma stocks like UCB (UCBJF) look well
positioned with a Zacks Rank #1 (Strong Buy).
ACORDA THERAPT (ACOR): Free Stock Analysis Report
BIOGEN IDEC INC (BIIB): Free Stock Analysis Report
NOVARTIS AG-ADR (NVS): Free Stock Analysis Report
UCB SA (UCBJF): Get Free Report
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