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Incyte: Pivotal Phase 3 Data Showing Significant Improvements in Facial and Total Body Repigmentation with Ruxolitinib Cream (Opzelura) in Vitiligo Published in New England Journal of Medicine

Data served as basis for recent FDA approval of ruxolitinib cream (Opzelura) 1.5% for the topical treatment of nonsegmental vitiligo in adult and pediatric patients 12 years of age and older Fifty-two
United States Erica Cech Catalina Loveman David Rosmarin Christine Chiou Jim Lee

Helsinn Healthcare S.A.: Helsinn publishes new data evaluating chlormethine gel's mode of action in Dermatology and Therapy

Helsinn publishes new data evaluating chlormethine gel's mode of action in Dermatology and Therapy Lugano, Switzerland, October 18, 2022 - Helsinn Group ("Helsinn"), a fully integrated, global
United States Alessandro Alonzi Pablol Ortiz Romero Kostenloser Wertpapierhandel Paola Bonvicini Stefano Frizzarin

Moderna, Inc.: Merck and Moderna Announce Exercise of Option by Merck for Joint Development and Commercialization of Investigational Personalized Cancer Vaccine

Companies on track to report data from the ongoing Phase 2 trial of mRNA-4157/V940 in combination with KEYTRUDA® as adjuvant therapy in high-risk melanoma in 4Q 2022CAMBRIDGE, MA and RAHWAY, NJ / ACCESSWIRE
United States United Kingdom Lavina Talukdar Julie Cunningham Mary Beth Woodin Eliav Barr

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Johnson & Johnson : Results of Novel Clinical Study of Guselkumab and Golimumab Combination Therapy Show Adults with Moderately to Severely Active Ulcerative Colitis Maintained Higher Rates of Clinical, Histologic, and Endoscopic Remission at Week 38

The rate of clinical remission was 47.9 percent in patients who received combination induction therapy with guselkumab and golimumab compared with either treatment alone at 38 weeks1 ... | October 10, 2022
United States Spring House Craig Stoltz Brucee Sands None Of The Janssen Pharmaceutical Companies Crohn Colitis Foundation

Aytu BioPharma, Inc.: Aytu BioPharma Announces Continuing Availability of ADHD Medication Adzenys XR-ODT in Response to Reported Generic Adderall XR Supply Disruptions

Adzenys XR-ODT is FDA-Approved as Bioequivalent to Adderall XRReported Supply Disruptions of Adderall XR Generic Equivalents Have the Potential to Affect Patient Access to ADHD MedicationsENGLEWOOD, CO
United States Grand Prairie Aytu Biopharma Roger Weiss Mark Oki Josh Disbrow

MorphoSys Presents New Long-Term Data from L-MIND Suggesting Durable Response to Treatment with Monj

EQS-News: MorphoSys AG / Key word(s): MiscellaneousMorphoSys Presents New Long-Term Data from L-MIND Suggesting Durable Response to Treatment with Monjuvi® (tafasitamab-cxix) for Patients with R/R DLBCL 28.09.2022 / 22:01 CET/CESTThe issuer is solely responsible for the content of this announcement.Media Release BOS...
United States United Kingdom Johannes Duell Kaitlyn Nealy Thomas Biegi Julia Neugebauer

MorphoSys Presents New Long-Term Data from L-MIND Suggesting Durable Response to Treatment with Monjuvi (tafasitamab-cxix) for Patients with R/R DLBCL

BOSTON - MorphoSys USA, Inc., a fully owned subsidiary of MorphoSys AG , announced data from the ongoing L-MIND study showing that Monjuvi plus lenalidomide followed by Monjuvi monotherapy provided... | September 29, 2022
United States United Kingdom Kaitlyn Nealy Thomas Biegi Johannes Duell Julia Neugebauer

MorphoSys Presents New Long-Term Data from L-MIND Suggesting Durable Response to Treatment with Monjuvi® (tafasitamab-cxix) for Patients with R/R DLBCL - MorphoSys (NASDAQ:MOR) - Press Release

The findings, including data from patients treated with the targeted immunotherapy for 5 years or more, will be presented during the Tenth Annual Meet
United States United Kingdom Johannes Duell Development Officer Xencor Inc Drug Administration

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