Solymbic

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On 26 January 2017, the Committee for Medicinal Products for Human Use (CHMP) adopted a positive opinion, recommending the granting of a marketing authorisation for the medicinal product Solymbic, intended for the treatment of rheumatoid arthritis, enthesitis-related arthritis, axial spondyloarthritis, psoriatic arthritis, psoriasis, hidradenitis suppurativa, Crohn’s disease, ulcerative colitis and uveitis. The applicant for this medicinal product is Amgen Europe B.V.

Solymbic will be available as a solution for injection (20 mg and 40 mg). The active substance of Solymbic is adalimumab, a tumour necrosis factor alpha (TNF╬▒) inhibitor (ATC code: L04AB04). Adalimumab binds specifically to TNF and neutralises the biological function of TNF by blocking its interaction with the p55 and p75 cell surface TNF receptors. Adalimumab also modulates biological responses that are induced or regulated by TNF, including changes in the levels of adhesion molecules responsible for leucocyte migration (ELAM-1, VCAM-1, and ICAM-1).

Solymbic is a biosimilar medicinal product that is highly similar to the reference product Humira (adalimumab), which was authorised in the EU on 8 September 2003. Studies have shown that Solymbic has comparable quality, safety and efficacy to Humira.

The full indication is:

“Rheumatoid arthritis

Solymbic in combination with methotrexate is indicated for:

  • the treatment of moderate to severe, active rheumatoid arthritis in adult patients when the response to disease-modifying anti-rheumatic drugs including methotrexate has been inadequate.
  • the treatment of severe, active and progressive rheumatoid arthritis in adults not previously treated with methotrexate.

Solymbic can be given as monotherapy in case of intolerance to methotrexate or when continued treatment with methotrexate is inappropriate.

Solymbic reduces the rate of progression of joint damage as measured by x-ray and improves physical function, when given in combination with methotrexate.

Juvenile idiopathic arthritis

Enthesitis-related arthritis

Solymbic is indicated for the treatment of active enthesitis-related arthritis in patients, 6 years of age and older, who have had an inadequate response to, or who are intolerant of, conventional therapy (see section 5.1).

Axial spondyloarthritis

Ankylosing spondylitis (AS)

Solymbic is indicated for the treatment of adults with severe active ankylosing spondylitis who have had an inadequate response to conventional therapy.

Axial spondyloarthritis without radiographic evidence of AS

Solymbic is indicated for the treatment of adults with severe axial spondyloarthritis without radiographic evidence of AS but with objective signs of inflammation by elevated CRP and/or MRI, who have had an inadequate response to, or are intolerant to non-steroidal anti-inflammatory drugs.

Psoriatic arthritis

Solymbic is indicated for the treatment of active and progressive psoriatic arthritis in adults when the response to previous disease-modifying anti-rheumatic drug therapy has been inadequate. Solymbic reduces the rate of progression of peripheral joint damage as measured by x-ray in patients with polyarticular symmetrical subtypes of the disease (see section 5.1) and improves physical function.

Psoriasis

Solymbic is indicated for the treatment of moderate to severe chronic plaque psoriasis in adult patients who are candidates for systemic therapy.

Paediatric plaque psoriasis

Solymbic is indicated for the treatment of severe chronic plaque psoriasis in children and adolescents from 4 years of age who have had an inadequate response to or are inappropriate candidates for topical therapy and phototherapies.

Hidradenitis suppurativa (HS)

Solymbic is indicated for the treatment of active moderate to severe hidradenitis suppurativa (acne inversa) in adult patients with an inadequate response to conventional systemic HS therapy.

Crohn’s disease

Solymbic is indicated for treatment of moderately to severely active Crohn’s disease, in adult patients who have not responded despite a full and adequate course of therapy with a corticosteroid and/or an immunosuppressant; or who are intolerant to or have medical contraindications for such therapies.

Paediatric Crohn's disease

Solymbic is indicated for the treatment of moderately to severely active Crohn's disease in paediatric patients (from 6 years of age) who have had an inadequate response to conventional therapy including primary nutrition therapy, a corticosteroid, and an immunomodulator, or who are intolerant to or have contraindications for such therapies.

Ulcerative colitis

Solymbic is indicated for treatment of moderately to severely active ulcerative colitis in adult patients who have had an inadequate response to conventional therapy including corticosteroids and 6-mercaptopurine (6-MP) or azathioprine (AZA), or who are intolerant to or have medical contraindications for such therapies.

Uveitis

Solymbic is indicated for the treatment of non-infectious intermediate, posterior and panuveitis in adult patients who have had an inadequate response to corticosteroids, in patients in need of corticosteroid-sparing, or in whom corticosteroid treatment is inappropriate.”

Solymbic treatment should be initiated and supervised by specialist physicians experienced in the diagnosis and treatment of conditions for which Solymbic is indicated.

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.

Name Language First published Last updated
CHMP summary of positive opinion for Solymbic (English only) 2017-01-27  

Key facts

Product details for Solymbic
NameSolymbic
INN or common name

adalimumab

Therapeutic area Spondylitis, AnkylosingArthritis, RheumatoidHidradenitis SuppurativaColitis, UlcerativeArthritis, PsoriaticCrohn DiseasePsoriasis
Active substance

adalimumab

Date opinion adopted26/01/2017
Company name

Amgen Europe B.V.

StatusPositive
Application typeInitial authorisation