La nuova combinazion
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
04 oct. 2024 16h28 HE | Janssen Cilag International NV
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) --...
Neue Kombination aus
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
04 oct. 2024 16h28 HE | Janssen Cilag International NV
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...
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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
27 sept. 2024 08h21 HE | Janssen Cilag International NV
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) --...
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Nipocalimab pivotal Phase 3 trial demonstrates sustained disease control in FcRn class for a broad population of myasthenia gravis patients
28 juin 2024 12h09 HE | Janssen Cilag International NV
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...
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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
14 juin 2024 03h00 HE | Janssen Cilag International NV
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...
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Johnson & Johnson MedTech gathers multi-disciplinary expert group to optimise lung cancer care and dialogue between patients and their healthcare team
30 mai 2024 08h39 HE | Johnson & Johnson MedTech
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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Johnson & Johnson submits regulatory applications to European Medicines Agency for TREMFYA® (guselkumab) for treatment of patients with ulcerative colitis and Crohn’s disease
01 mai 2024 06h55 HE | Janssen Cilag International NV
        Media contact:Sophie DaneauSdaneau@its.jnj.com+33 6 3178 8798Investor contact:Raychel Kruperinvestor-relations@its.jnj.com For European and UK medical and trade media only For immediate...
SWAV Alert: Monsey Firm of Wohl & Fruchter Investigating Fairness of the Sale of Shockwave Medical to Johnson & Johnson
10 avr. 2024 09h25 HE | Wohl & Fruchter LLP
We are investigating the fairness of the price of $335.00 per share in cash for which Shockwave Medical has agreed to be sold to Johnson & Johnson.
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CURE Media Group and Oncology Nursing News Announces the 2024 Extraordinary Healer® Award Finalists
15 mars 2024 12h00 HE | CURE Media Group
CRANBURY, N.J., March 15, 2024 (GLOBE NEWSWIRE) -- CURE® Media Group, the industry-leading multimedia platform devoted to providing cancer updates and research to more than 1 million patients,...