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DIR Return to: LEMTRADA (Campath, alemtuzumab)
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#Post#: 1197--------------------------------------------------
(AAN) 10-year follow-up data on Lemtrada
DIR By: agate
Date: April 28, 2016, 2:08 pm
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From Medical News Today, April 20, 2016:
--- Quote ---
> Multiple sclerosis: 10-year follow-up data on Lemtrada
(alemtuzumab) presented at the AAN 2016 Annual Meeting
>
>
> Adapted Media Release
>
> Sanofi Genzyme, the specialty care global business unit of
Sanofi, has announced that a new long-term analysis detailing 10
years of clinical efficacy of Lemtrada® (alemtuzumab) in people
with relapsing-remitting multiple sclerosis (RRMS) will be
presented at the 68th American Academy of Neurology (AAN) 2016
Annual Meeting in Vancouver, Canada, 15-21 April 2016.
>
> Results from the on-going, long-term extension study of the
phase 2 CAMMS223 study showed that over 10 years of follow-up,
76 percent of patients were shown to be free from 6-month
confirmed disability worsening (increase of ≥1.0 EDSS
point [or ≥1.5 points if baseline EDSS=0]) and 78 percent
had an Expanded Disability Status Scale [EDSS] score that was
either stable or showed greater than or equal to one point
improvement in EDSS vs baseline.
>
> In addition, a low annualised relapse rate (ARR) was
maintained (0.08) over the period. The long-term safety observed
in this group of patients was in line with that of other
Lemtrada clinical trials.
>
> People who entered the CAMMS223 study had not previously
received other treatments for RRMS and the majority of those who
were followed for 10 years received a maximum of three courses
of Lemtrada.
>
> "These data provide further evidence of the long term response
with Lemtrada in treatment-naïve patients with
relapsing-remitting MS", said Professor Alasdair Coles, Lead
Investigator, University of Cambridge School of Clinical
Medicine, Cambridge, UK. "It is remarkable that such infrequent
dosing with Lemtrada offers stability or improvement of
disability over ten years. These findings confirm that Lemtrada
is a valid treatment approach for people with multiple
sclerosis, without the need for continuous treatment."
>
> "We are very pleased with these new data, which are part of
our extensive clinical development programme and our commitment
to the field of MS," commented Peter Kuiper, General Manager UK
& Ireland at Sanofi Genzyme. "Being able to offer this treatment
option, which was discovered and developed in the UK to
clinicians and their patients, is of incredible importance to
us."
>
> The data on Durable Efficacy of Alemtuzumab Over 10 Years:
Long-Term Follow-Up of Patients with RRMS from the CAMMS223
Study was presented as a poster presentation on Monday, 18 April
2016.
>
> More than 100,000 people in the UK have Multiple Sclerosis
(MS), with around 85 percent diagnosed with RRMS. Lemtrada is
the second of Sanofi Genzyme's treatments for MS to receive
approval for use from NICE and on the NHS in England and Wales.
--- End Quote ---
[References omitted]
The article can be seen here
HTML http://www.medicalnewstoday.com/releases/309335.php.
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