- VKTX Q1 Earnings Miss on Higher Phase 3 Development Costs
Apr 30, 2026 · zacks.com
Viking Therapeutics posts a wider Q1 loss as R&D spend jumps on Phase III obesity drug work, while it advances VK2735 studies and preps oral late-stage study.
- Merck Receives Two Positive EU CHMP Opinions for KEYTRUDA® (pembrolizumab), for Subcutaneous (SC) Administration and for New Indication for Earlier-Stage Head and Neck Cancer
Sep 19, 2025 · businesswire.com
RAHWAY, N.J.--(BUSINESS WIRE)---- $MRK #MRK--Merck (NYSE: MRK), known as MSD outside of the United States and Canada, today announced that the European Medicines Agency's Committee for Medicinal Products for Human Use (CHMP) adopted two positive opinions for KEYTRUDA® (pembrolizumab), Merck's anti-PD-1 therapy. One recommends approval of a new subcutaneous (SC) route of administration and a new pharmaceutical form (solution for injection) for KEYTRUDA® (pembrolizumab), which if approved would be marketed in.
- MERCK RECEIVES TWO POSITIVE EU CHMP OPINIONS FOR KEYTRUDA® (PEMBROLIZUMAB), FOR SUBCUTANEOUS (SC) ADMINISTRATION AND FOR NEW INDICATION FOR EARLIER-STAGE HEAD AND NECK CANCER
Sep 19, 2025
RAHWAY, N.J.--(BUSINESS WIRE)---- $MRK #MRK--MERCK (NYSE: MRK), KNOWN AS MSD OUTSIDE OF THE UNITED STATES AND CANADA, TODAY ANNOUNCED THAT THE EUROPEAN MEDICINES AGENCY'S COMMITTEE FOR MEDICINAL PRODUCTS FOR HUMAN USE (CHMP) ADOPTED TWO POSITIVE OPINIONS FOR KEYTRUDA® (PEMBROLIZUMAB), MERCK'S ANTI-PD-1 THERAPY. ONE RECOMMENDS APPROVAL OF A NEW SUBCUTANEOUS (SC) ROUTE OF ADMINISTRATION AND A NEW PHARMACEUTICAL FORM (SOLUTION FOR INJECTION) FOR KEYTRUDA® (PEMBROLIZUMAB), WHICH IF APPROVED WOULD BE MARKETED IN.
- Santander Consumer Launches Drive Together, Offering Dealers Pre-Qualified Leads from Web Traffic
Jul 8, 2025 · businesswire.com
DALLAS--(BUSINESS WIRE)--Santander Consumer USA Inc. (“Santander Consumer”) has launched Drive Together, a digital retail tool and expansion of Santander's Drive® offering that provides pre-qualification resources to support a broad range of customer and dealer needs. Drive Together is a subscription service for dealers that resides on car dealerships' websites, allowing dealers to generate pre-qualified leads from their web traffic. Santander's Drive® platform uses "soft" credit checks to preq.
- SANTANDER CONSUMER LAUNCHES DRIVE TOGETHER, OFFERING DEALERS PRE-QUALIFIED LEADS FROM WEB TRAFFIC
Jul 8, 2025
DALLAS--(BUSINESS WIRE)--SANTANDER CONSUMER USA INC. (“SANTANDER CONSUMER”) HAS LAUNCHED DRIVE TOGETHER, A DIGITAL RETAIL TOOL AND EXPANSION OF SANTANDER'S DRIVE® OFFERING THAT PROVIDES PRE-QUALIFICATION RESOURCES TO SUPPORT A BROAD RANGE OF CUSTOMER AND DEALER NEEDS. DRIVE TOGETHER IS A SUBSCRIPTION SERVICE FOR DEALERS THAT RESIDES ON CAR DEALERSHIPS' WEBSITES, ALLOWING DEALERS TO GENERATE PRE-QUALIFIED LEADS FROM THEIR WEB TRAFFIC. SANTANDER'S DRIVE® PLATFORM USES "SOFT" CREDIT CHECKS TO PREQ.
- TREMFYA® (guselkumab) subcutaneous (SC) induction data support potential to be the first and only in its class to offer the option of both intravenous and SC induction therapy in ulcerative colitis
Feb 21, 2025 · prnewswire.com
Phase 3 ASTRO study achieves primary and all secondary endpoints at Week 12 in ulcerative colitis patients The only SC induction data for an IL-23 inhibitor show statistically significant and clinically meaningful improvements across clinical and endoscopic measures versus placebo, consistent with IV induction SPRING HOUSE, Pa. , Feb. 21, 2025 /PRNewswire/ -- Johnson & Johnson (NYSE: JNJ) today announced data from the Phase 3 ASTRO study of TREMFYA® (guselkumab) subcutaneous (SC) induction therapy in adults with moderately to severely active ulcerative colitis (UC) at the 20th Congress of the European Crohn's and Colitis Organization (ECCO).
- TREMFYA® (GUSELKUMAB) SUBCUTANEOUS (SC) INDUCTION DATA SUPPORT POTENTIAL TO BE THE FIRST AND ONLY IN ITS CLASS TO OFFER THE OPTION OF BOTH INTRAVENOUS AND SC INDUCTION THERAPY IN ULCERATIVE COLITIS
Feb 21, 2025
PHASE 3 ASTRO STUDY ACHIEVES PRIMARY AND ALL SECONDARY ENDPOINTS AT WEEK 12 IN ULCERATIVE COLITIS PATIENTS THE ONLY SC INDUCTION DATA FOR AN IL-23 INHIBITOR SHOW STATISTICALLY SIGNIFICANT AND CLINICALLY MEANINGFUL IMPROVEMENTS ACROSS CLINICAL AND ENDOSCOPIC MEASURES VERSUS PLACEBO, CONSISTENT WITH IV INDUCTION SPRING HOUSE, PA. , FEB. 21, 2025 /PRNEWSWIRE/ -- JOHNSON & JOHNSON (NYSE: JNJ) TODAY ANNOUNCED DATA FROM THE PHASE 3 ASTRO STUDY OF TREMFYA® (GUSELKUMAB) SUBCUTANEOUS (SC) INDUCTION THERAPY IN ADULTS WITH MODERATELY TO SEVERELY ACTIVE ULCERATIVE COLITIS (UC) AT THE 20TH CONGRESS OF THE EUROPEAN CROHN'S AND COLITIS ORGANIZATION (ECCO).
- Telsey Advisory Group LLC announces U.S. Equity Research alliance with Santander
Dec 16, 2024 · businesswire.com
NEW YORK--(BUSINESS WIRE)--Telsey Advisory Group LLC (TAG) announced today that it has entered a strategic alliance with Santander's U.S. broker-dealer subsidiary Santander U.S. Capital Markets LLC. TAG is a recognized leader in the consumer sector, with an established track record, highly regarded analysts, and a clear vision for expansion. TAG, founded in 2006 by Dana Telsey, is a leading equity research firm, with a strong institutional equity sales and agency trading platform focused on the.
- TELSEY ADVISORY GROUP LLC ANNOUNCES U.S. EQUITY RESEARCH ALLIANCE WITH SANTANDER
Dec 16, 2024
NEW YORK--(BUSINESS WIRE)--TELSEY ADVISORY GROUP LLC (TAG) ANNOUNCED TODAY THAT IT HAS ENTERED A STRATEGIC ALLIANCE WITH SANTANDER'S U.S. BROKER-DEALER SUBSIDIARY SANTANDER U.S. CAPITAL MARKETS LLC. TAG IS A RECOGNIZED LEADER IN THE CONSUMER SECTOR, WITH AN ESTABLISHED TRACK RECORD, HIGHLY REGARDED ANALYSTS, AND A CLEAR VISION FOR EXPANSION. TAG, FOUNDED IN 2006 BY DANA TELSEY, IS A LEADING EQUITY RESEARCH FIRM, WITH A STRONG INSTITUTIONAL EQUITY SALES AND AGENCY TRADING PLATFORM FOCUSED ON THE.
- Celltrion presents 2-year post-hoc analysis findings for subcutaneous infliximab (CT-P13 SC), highlighting dose escalation as an option for managing loss of response in inflammatory bowel disease
Oct 15, 2024 · businesswire.com
INCHEON, South Korea--(BUSINESS WIRE)--Celltrion today announced two-year results of subcutaneous infliximab (CT-P13 SC) dose escalation therapy at United European Gastroenterology (UEG) Week 2024 in Vienna. The post-hoc analysis from the LIBERTY-CD (Crohn's disease) and LIBERTY-UC (ulcerative colitis) studies suggest that dose escalation of CT-P13 SC following intravenous (IV) induction in patients who initially respond but subsequently lose response, showed clinical efficacy over an extended.