MUNSTER, IN / ACCESSWIRE / June 12, 2024 / OptiMed HealthCare Partners is pleased to announce the opening of its new center in Munster, Indiana. SPRAVATO® is the first FDA-approved nasal spray for treatment-resistant depression (TRD). OptiMed is proud to lead the change in mental health care by expanding this treatment to Munster, IN.
Comments: Innovative Medicine sales were up 1% to $13.6 billion in the quarter. DARZALEX (daratumumab) sales were $2.7 billion, up 19%. ERLEADA (apalutamide) sales were $689 million, up 27%. CARVYKTI (ciltacabtagene autoleucel) sales were $157 million, up from $72 million in 1Q23. TECVAYLI (teclistamab-cqyv) sales were $133 million, up from 63 million in 1Q23. Other Oncology sales were $178 million, up 80% in the quarter. UPTRAVI (selexipag) sales were up 29% to $468 million and OPSUMIT (macitentan) sales were up 19% to $524 million. TREMFYA (guselkumab) sales were up 26% to $808 million. SPRAVATO (esketamine) sales were up 72% to $225 million. COVID-19 Vaccine sales were down 97% to $25 million. XARELTO sales were down 10% to $518 million. REMICADE sales were down 11% to $434 million. ZYTIGA sales were down 26% to $181 million. CONCERTA sales were down 14% to $177 million.
BEERSE, BELGIUM, 8 October 2023 – The Janssen Pharmaceutical Companies of Johnson & Johnson today announced further findings for SPRAVATO® (esketamine nasal spray [NS]) from the ESCAPE-TRD study. Data on treatment-emergent adverse events (TEAEs) suggest a more favourable tolerability profile in adults with treatment-resistant major depressive disorder (TRD) receiving esketamine NS than quetiapine XR. Across all reported TEAEs experienced with esketamine NS, 92.1 percent were transient and resolved the same-day vs 12.1 percent of TEAEs experienced with quetiapine XR.1 The findings were presented at the 36th European College of Neuropsychopharmacology Congress (ECNP 2023) taking place from 7 October to 10 October in Barcelona, Spain.
FDA Confirms Paragraph IV Patent Litigation for Esketamine Hydrochloride
(Yicai Global) April 21 -- China has given the green light to the local unit of Janssen Pharmaceuticals, owned by US medical device and drug developer Johnson & Johnson, to market its new antidepressant in the country.
New Data from the Phase 3b ESCAPE-TRD Study Show that Participants Receiving SPRAVATO®▼(Esketamine Nasal Spray [NS]) Achieved Higher Response and Remission Rates, Increasing Over Time, Compared to those Receiving Quetiapine Extended-Release
Janssen’s SPRAVATO® (esketamine nasal spray [NS]) helped more participants with treatment-resistant major depressive disorder (TRD) remain remission and relapse free compared with quetiapine extended-release (XR), both in combination with a continuing selective serotonin reuptake inhibitor (SSRI) or serotonin and norepinephrine reuptake inhibitor (SNRI), in a Phase III trial (04338321).
The Janssen Pharmaceutical Companies of Johnson & Johnson has reported that the Phase IIIb ESCAPE-TRD clinical trial of Spravato (esketamine nasal spray [NS]) for treatment-resistant major depressive disorder (TRD) in adult patients met its primary endpoint.
Johnson & Johnson’s esketamine nasal spray continues to build a body of evidence showing it can go toe-to-toe with tough-to-treat depression.
SPRAVATO®? (esketamine nasal spray) data from the phase 3b ESCAPE-TRD study demonstrate superior efficacy compared to quetiapine extended-release in treatment-resistant major depressive disorder1