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Nordimet (Mtx) gets positive from EU for psoriasis

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Nordimet (Mtx) gets positive from EU for psoriasis
Fred Offline
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#1
News  Mon-27-06-2016, 12:34 PM
Nordimet (Methotrexate) has been given positive opinion from the Committee for Medicinal Products for Human Use (CHMP) for use in psoriatic arthritis.

Quote:
The Committee for Medicinal Products for Human Use (CHMP) adopted a positive opinion, recommending the granting of a marketing authorisation for the medicinal product Nordimet, intended for the treatment of active rheumatoid arthritis, juvenile idiopathic arthritis, and severe psoriatic arthritis. The applicant for this medicinal product is Nordic Group B.V.

Nordimet will be available as a solution for injection (7.5 mg, 10 mg, 12.5 mg, 15 mg, 17.5 mg, 20 mg, 22.5 mg and 25 mg). The active substance of Nordimet is methotrexate, an anti-metabolite folic acid analogue (ATC code: L01BA01) which inhibits DNA synthesis through the competitive inhibition of the enzyme dihydrofolate reductase.

The benefits with Nordimet are its ability to reduce the symptoms of rheumatoid arthritis, psoriasis and psoriatic arthritis. The most common side effects are abnormal liver function tests, stomatitis, dyspepsia, nausea, abdominal pain and loss of appetite.

Nordimet is a hybrid of Lantarel FS (25 mg solution for injection), a medicine containing the same active substance that has been authorised in Germany since 1992.

'Nordimet is indicated for the treatment of: active rheumatoid arthritis in adult patients, polyarthritic forms of severe, active juvenile idiopathic arthritis (JIA), when the response to nonsteroidal anti-inflammatory drugs (NSAIDs) has been inadequate, severe recalcitrant disabling psoriasis, which is not adequately responsive to other forms of therapy such as phototherapy, PUVA, and retinoids, and severe psoriatic arthritis in adult patients.'

It is proposed that Nordimet be prescribed by physicians with experience in the various properties of the medicinal product and its mode of action.

Detailed recommendations for the use of this product will be described in the summary of product characteristics (SmPC), which will be published in the European public assessment report (EPAR) and made available in all official European Union languages after the marketing authorisation has been granted by the European Commission.

Source: ema.europa.eu

sick
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jiml Offline
100 + Member I Just Cant Stop !

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#2
Mon-27-06-2016, 12:50 PM
Not a favourite if mine but it might be the one thing that works for some people ...... Confused
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Caroline Offline
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#3
Mon-27-06-2016, 12:50 PM
I bet that in the committee there are no persons with psoriatic arthritis who are being treated with Nordibet. Angry
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D Foster Offline
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#4
Mon-27-06-2016, 13:07 PM (This post was last modified: Mon-27-06-2016, 13:07 PM by D Foster.)
I thought that it said CHIMP had recommended it , I wondered if animal testing had taken a different direction.
It does have a place and has been a savoir for quite a lot of people , my doctor uses it for arthritis and he thinks that it is a good option compared to many other treatments.
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mataribot Offline
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#5
Mon-27-06-2016, 16:30 PM
MTX is not DMARD drug in PsA - it does slow down or prevent bone damage. It may make some people feel better, but I am guessing that's the placebo effect.
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