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28 mars 2025 07h20 HE | Source: Janssen Cilag International NV

TREMFYA® (guselkumab) receives positive CHMP opinion for treatment of patients with moderately to severely active Crohn’s Disease

Recommendation based on the findings from the Phase 3 studies (GALAXI programme and GRAVITI) in Crohn’s disease 1,2,3 Beerse, Belgium (28 March 2025) – Johnson & Johnson today announced that the...
28 févr. 2025 08h43 HE | Source: Janssen Cilag International NV

TREMFYA® (guselkumab) receives positive CHMP opinion for treatment of adult patients with moderately to severely active ulcerative colitis

Recommendation based on the findings from the Phase 3 QUASAR programme in ulcerative colitis1 Beerse, Belgium (28 February 2025) – Johnson & Johnson today announced that the Committee for...
23 janv. 2025 05h45 HE | Source: Janssen Cilag International NV

Findings from pivotal nipocalimab Phase 3 study in a broad antibody positive population of people living with generalised myasthenia gravis published in The Lancet Neurology

The first investigational FcRn blocker to demonstrate sustained disease control over 24 weeks in antibody positive adult patients: anti-AChR+, anti-MuSK+, anti-LRP4+ Nipocalimab demonstrated a...
04 oct. 2024 16h28 HE | Source: Janssen Cilag International NV

La nuova combinazione di TALVEY®▼ (talquetamab) e TECVAYLI®▼ (teclistamab) comporta alti tassi di risposta e risposte durature in pazienti refrattari alla tripla classe con mieloma multiplo recidivato o refrattario, compresi i pazienti con malattia extramidollare

I dati dello studio sperimentale di Fase 1b RedirecTT-1 dimostrano un profilo di sicurezza coerente con le monoterapie talquetamab e teclistamab1 BEERSE, BELGIO, Oct. 04, 2024 (GLOBE NEWSWIRE) --...
04 oct. 2024 16h28 HE | Source: Janssen Cilag International NV

Neue Kombination aus TALVEY®▼(talquetamab) und TECVAYLI®▼ (teclistamab) deutet auf hohe Ansprechraten und ein dauerhaftes Ansprechen bei Tripe-Class-refraktären Patienten mit rezidiviertem oder refraktärem Multiplem Myelom, einschließlich Patienten mit extramedullärer Erkrankung

Daten aus der Phase-Ib-Forschungsstudie RedirecTT-1 zeigen ein mit dem von talquetamab und teclistamab-Monotherapien vergleichbares Sicherheitsprofil1 BEERSE, BELGIEN, Oct. 04, 2024 (GLOBE...
04 oct. 2024 16h28 HE | Source: Janssen Cilag International NV

La nouvelle association de TALVEY®▼ (talquétamab) et TECVAYLI®▼ (teclistamab) suggère des taux de réponse élevés et des réponses durables chez les patients réfractaires à trois classes de médicaments atteints d’un myélome multiple récidivant ou réfractaire, y compris les patients atteints d’une maladie extramédullaire

Les données issues de l’étude expérimentale de Phase Ib RedirecTT-1 démontrent un profil d’innocuité cohérent avec les monothérapies par talquétamab et teclistamab1 BEERSE, BELGIQUE, 04 oct. 2024 ...
27 sept. 2024 08h21 HE | Source: Janssen Cilag International NV

Novel combination of TALVEY®▼ (talquetamab) and TECVAYLI®▼ (teclistamab) suggest high response rates and durable responses in triple-class refractory patients with relapsed or refractory multiple myeloma, including those with extramedullary disease

Data from the investigational Phase 1b RedirecTT-1 study demonstrate a safety profile consistent to talquetamab and teclistamab monotherapies1 BEERSE, BELGIUM, Sept. 27, 2024 (GLOBE NEWSWIRE) --...
28 juin 2024 12h09 HE | Source: Janssen Cilag International NV

Nipocalimab pivotal Phase 3 trial demonstrates sustained disease control in FcRn class for a broad population of myasthenia gravis patients

First FcRn blocker to demonstrate superiority in Myasthenia Gravis - Activities of Daily Living score (MG-ADL) a over placebo when added to standard of care over 24 weeks in antibody positive...
14 juin 2024 03h00 HE | Source: Janssen Cilag International NV

Findings from landmark RESONATE-2 study confirm sustained survival benefit of IMBRUVICA® (ibrutinib) for first-line chronic lymphocytic leukaemia treatment with up to 10 years follow-up

RESONATE-2 data presented at the 2024 European Hematology Association (EHA) Congress provide longest-term outcomes and safety data ever reported for a monotherapy BTK inhibitor, with a median PFS of...
30 mai 2024 08h39 HE | Source: Johnson & Johnson MedTech

Johnson & Johnson MedTech gathers multi-disciplinary expert group to optimise lung cancer care and dialogue between patients and their healthcare team

A recent European survey revealed that 80 percent of thoracic surgeons declared to follow the Enhanced Recovery After Surgery (ERAS) protocol, focussed on improving peri-operative lung cancer care,1...

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