Press release – First marketing authorisation worldwide for methotrexate in moderate psoriasis

Medac’s marketing authorisation extension gives many patients with psoriasis access to guidelines-based MTX therapy for the first time.


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Press release – Results of phase III study with Treosulfan, EMA approval pending

Highly effective with reduced toxicity – Treosulfan-based regimen is a promising new conditioning therapy for MDS and AML


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Press release – Medac Finland – 10-years anniversary symposium

Enhancing the potential of methotrexate.

Optimise  rheumatism  treatment  in  Finland  with  Metoject®   PEN1   and ensure long-term success of therapy

Helsinki / Wedel (September 21, 2017). There is room for improvement in drug treatment of rheumatoid arthritis (RA) with the gold standard methotrexate (MTX). Current analyses of the FIN-ERA cohort suggest that Finnish rheumatology exploits the potential of methotrexate as initial treatment and follows the European treatment guidelines in a slightly adopted way focusing on combination therapy: “At baseline, 68 % used methotrexate-based combination therapy, and 31 % used triple therapy with methotrexate, hydroxychloroquine, and sulphasalazine (the Fin-RACo regimen)”.

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Press release – Medac at the EADV 2017

Methotrexate for psoriasis: effective, safe, favourable.

Medac with recent data on subcutaneous methotrexate from METOP study at the EADV in Geneva.

Geneva / Wedel (September 15, 2017). Methotrexate (MTX) is the most frequently used conventional systemic drug in the treatment of psoriasis. With over 50 years of successful experience in this setting, it is no wonder that recent treatment recommendations consider MTX as first-line and cost-effective therapeutic for the systemic treatment of psoriasis. And still the potential of MTX is often not fully exploited. In particular the dose and route of administration are aspects that should be considered.

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Press release – Medac at DGRh 2017

Enhancing the potential of methotrexate.

Optimise rheumatism treatment with Metoject® and ensure long-term success of therapy

Stuttgart / Wedel (September 11, 2017). There is room for improvement in drug treatment of rheumatoid arthritis (RA) with the gold standard methotrexate (MTX). Current analyses of the CAPEA cohort suggest that German rheumatology exploits the potential of methotrexate as initial treatment and follows the treatment guidelines closely: “After 3 months, 82 % of patients with a diagnosis of RA were given first line treatment with methotrexate. […] In 78 % of the patients treated with methotrexate, the starting dose was 15 mg weekly”. Long-term data from the core documentation also confirm at 61 % the great importance of MTX in the treatment  of RA. Current data from  a German health insurance, however, paint  a dramatically different picture nationwide. Given that csDMARDS account for 35 % of drug treatment, Germany is some way from appropriate therapeutic treatment of patients with rheumatoid arthritis.

The symposium on methotrexate sponsored by Medac at the DGRh congress in Stuttgart addressed this issue. As well as a new research project on the actual medical treatment situation, various options for improving the first line therapy with MTX were revealed.

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Press Release – medac at the BAD meeting 2017

Update on the first-line agent Methotrexate in psoriasis treatment: Intensified dosing and subcutaneous administration recommended

  • British Association of Dermatologists’ guidelines reaffirms the importance of the well- established and inexpensive first-line systemic agent Methotrexate (MTX) for the treatment of patients with all types of psoriasis
  • Recently in The Lancet published METOP trial meets the need of high-quality clinical trial with methotrexate in long-term therapy and shows lasting efficacy and safety of subcutaneous methotrexate over one year in an intensified dosing schedule

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Press Release – medac passes eco-audit

medac passes eco-audit and receives award for environmental management

medac Gesellschaft für klinische Spezialpräparate mbH is innovative, successful, sustainable and environment-friendly. The pharmaceutical company has proven that economic prosperity and environmental responsibility are not necessarily a contradiction. To achieve perfect conditions for this objective, medac subjected itself to an auditing procedure according to EMAS and DIN EN ISO 14001:2015 for the first time.

At the end of last year, all medac operating sites in Germany as well as the sites based in Europe successfully passed the inspection according to ISO 14001. In parallel, medac passed the strict Eco Management and Audit Scheme (EMAS) – better known as the EU eco-audit – in Germany.

The ISO 14001 standard is the internationally acknowledged and applied standard for operational environmental management. EMAS is a voluntary instrument of the European Union and also covers all the requirements of ISO 14001. This comprehensive environmental management and auditing system supports companies in keeping their environmental policy up-to-date, together with continuous improvement. Participating companies must record the effects of their activities with regard to the environment and prove having a process in place for the continuous improvement of their environmental performance. This is inspected and recertified in annual audits by independent auditors and environmental inspectors. Transparency is assured via the annually updated environmental declaration and registration in the EMAS register, both of which are accessible to the public.

The environmental declaration is now available on the medac website.

Caption: Presentation of the EMAS certificate to Mr Jörg Hans (right), Managing Director medac, by Dr Paul Raab, Head of the IHK (Chamber of Industry and Commerce) branch Elmshorn, in front of the new medac e-car, powered purely by electricity


Press Contact
Media Spokesperson
Volker Bahr
phone +49 (0)4103 – 8006  9111
fax +49 (0)4103 – 8006  8934
press(at)medac.de


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EADV 2016 – METOP study in medac satellite symposium

Benefits for psoriasis practices: New phase III data shows subcutaneous methotrexate’s favorable long-term efficacy and safety profile.

Medac hosted  a satellite symposium at the EADV conference 2016 in Vienna with the title METOP study – evaluation of subcutaneous methotrexate for psoriasis patients.

Satellite symposium took place on Friday 30th of September, 2016 at Hall L3, floor 1.

eadv-2016

Invitation to medac EADV 2016

medac press release EADV2016

More information about the congress

EULAR 2016 – medac satellite symposium

This will take place on Thursday the 9th of June 2016 at 8.15 am – 9.45, Room Capital Suite 2/4.
EULAR-inbjudan,-SE-NO-DK-2016-1

More information about the congress

 

Yhteistyö terveydenhuollon ammattilaisten kanssa

Taloudellisten tietojen julkistaminen – medac GmbH sivuliike Suomessa 2015

Taloudellisten tietojen julkistaminen – medac GmbH sivuliike Suomessa 2016

Muistio julkistamisessa käytetyistä menetelmistä