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Janssen EMEA

FMF World Congress 2023: Janssen shares new data in HDFN

27 June 2023 | By Catherine Eckford (European Pharmaceutical Review)

If approved, nipocalimab would be the first anti-FcRn therapy for EU pregnancies at high risk of haemolytic disease of the foetus and newborn.

article

Transforming oncology with antibody therapeutics

4 May 2023 | By Catherine Eckford (European Pharmaceutical Review), Martin Vogel (Janssen)

Martin Vogel, Therapeutic Area Lead for Oncology, Janssen EMEA, discusses the potential of bispecific monoclonal antibodies like amivantamab to address unmet needs in advanced non-small cell lung cancer treatment.

article

Treating multiple myeloma: An interview with Janssen

17 May 2017 | By Dr Catherine Taylor, Haematology Therapeutic Area Lead, Janssen EMEA

We caught up with Janssen's Dr Catherine Taylor to talk monoclonal antibodies, the rise of immuno-oncology and treating multiple myeloma...

news

EC approves Trevicta for the treatment of schizophrenia

1 June 2016 | By Victoria White, Digital Content Producer

The EC has approved the use of Trevicta (paliperidone palmitate a 3-monthly injection) for the maintenance treatment of schizophrenia in adult patients...

news

CHMP adopts positive opinion of Trevicta for maintenance treatment of schizophrenia

5 April 2016 | By Victoria White

If approved, this 3‑monthly injection will allow patients to maintain an optimal level of treatment in their blood with fewer administrations...

news

CHMP adopts positive opinion of Edurant in adolescents with HIV-1

26 October 2015 | By Victoria White

If approved by the European Commission, Edurant will become available for the treatment of adolescents with HIV-1 for the first time...

news

Janssen extends Blue Latitude contract

16 September 2015 | By Victoria White

Blue Latitude has been reappointed to provide Janssen with strategic support and creative marketing services for their brand teams in the EMEA region...

news

Janssen submits MAA for daratumumab to EMA

10 September 2015 | By Victoria White

Daratumumab is an investigational, human anti-CD38 monoclonal antibody, for the treatment of patients with relapsed and refractory multiple myeloma...

news

EC approves Stelara for the treatment of plaque psoriasis in adolescent patients

3 July 2015 | By Victoria White

The EC has approved Janssen’s Stelara for the treatment of moderate-to-severe plaque psoriasis in adolescent patients from the age of 12 years and older...

news

STELARA receives CHMP positive opinion for treatment of adolescents with moderate to severe psoriasis

27 May 2015 | By Victoria White

The CHMP has recommended approval of STELARA for the treatment of moderate to severe plaque psoriasis in adolescent patients aged 12 and older...

news

EU Disease Lens brings visibility and insight into the most critical diseases

24 March 2015 | By Victoria White

Janssen Health Policy Centre (Janssen Pharmaceutica NV) today unveiled the EU Disease Lens: a digital dashboard that brings insight into 15 major diseases...

news

New findings from the Psoriasis Longitudinal Assessment and registry (PSOLAR) show persistency difference among biologic therapies

10 October 2014 | By Janssen

Persistence of STELARA® (ustekinumab) significantly better than Anti-TNFs in treatment of Psoriasis according to observational study analysis...

news

New STELARA® (ustekinumab) five year data show consistent efficacy and safety profile in treatment of moderate to severe plaque psoriasis

7 June 2012 | By Publicis Life Brands Resolute

New efficacy and safety data...

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