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Merck Provides Update on KEYTRUDA® Indication in Third-Line Gastric Cancer in the US

Merck known as MSD outside the United States and Canada, today announced that the company plans to voluntarily withdraw the U.S. accelerated approval indication for KEYTRUDA for the treatment of patients with recurrent locally advanced or metastatic gastric or gastroesophageal junction adenocarcinoma whose tumors express PD-L1 [combined positive score ] as determined by a U.S. Food and Drug Administration -approved … Merck (NYSE: MRK), known as MSD outside the United States and Canada, today...
United States Scot Ebbinghaus Courtney Ronaldo Peter Dannenbaum Melissa Moody Merck Research Laboratories

Insulet : Omnipod® 5 Automated Insulin Delivery System Pivotal Studies Demonstrate Improved Outcomes Across the Lifespan from Ages 2 to 70 years

Insulet Corporation , the global leader in tubeless insulin pump technology with its Omnipod® brand of products, today announced promising results from its latest pivotal trial for the Omnipod 5... | June 27, 2021
United States Susanr Berman Davidj Kupfer Charlesf Reynolds Research Authors Danielj Buysse Exchange Commission On

Compugen Announces Updated Data from Phase 1 Study of COM701, First- in-Class Anti-PVRIG, at the ASCO 2021 Annual Meeting

Compugen Announces Updated Data from Phase 1 Study of COM701, First- in-Class Anti-PVRIG, at the ASCO 2021 Annual Meeting Font : A-A+ Data show ongoing durable responses beyond one year in monotherapy and in combination with Opdivo® in heavily pre-treated patients including one patient with prior progression on Opdivo® HOLON, Israel, June 8, 2021 /PRNewswire/ -- Compugen Ltd. (Nasdaq: CGEN) a clinical-stage cancer immunotherapy company and a leader in predictive target discovery, presented ...
Tel Aviv Daniel Vaena Compugen Ltd Corporate Communications Compugen Ltd Exchange Commission Securities Exchange

DURECT Corporation to Present Additional Clinical Data from DUR-928 Studies in NASH (Phase 1b) and in Hepatic Impairment (Phase 1) at Upcoming International Liver Conference 2021 (EASL)

Share this article Share this article CUPERTINO, Calif., June 9, 2021 /PRNewswire/ -- DURECT Corporation (Nasdaq: DRRX) today announced it will present two posters at the 2021 The first poster will discuss additional efficacy signals from a Phase 1b clinical study of orally administered DUR-928 in nonalcoholic steatohepatitis (NASH) patients. Previously reported data showed that DUR-928 was well tolerated at all three doses evaluated, 50mg QD, 150mg QD, and 300mg BID (600mg/day) with overall ...
United States Eric Lawitz Jaymin Shah Texas Liver Institute Drug Administration International Liver Conference

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Merck Announces Supply Agreement with U.S. Government for Molnupiravir, an Investigational Oral Antiviral Candidate for Treatment of Mild to Moderate COVID-19

Merck Announces Supply Agreement with U.S. Government for Molnupiravir, an Investigational Oral Antiviral Candidate for Treatment of Mild to Moderate COVID-19 U.S. government commits to purchase approximately 1.7 million courses of Molnupiravir upon issuance of Emergency Use Authorization or approval by the U.S. Food and Drug Administration Merck known as MSD outside the United States and Canada, today announced it has entered into a procurement agreement with the United States government for m...
United States Wendy Holman Ridgeback Biotherapeutics Peter Dannenbaum Melissa Moody Emory University

Lysogene Announces First Patient Dosed with LYS-GM101 Investigational Gene Therapy for the Treatment of GM1 Gangliosidosis

Lysogene Announces First Patient Dosed with LYS-GM101 Investigational Gene Therapy for the Treatment of GM1 Gangliosidosis Ongoing enrollment of a total of 16 patients in the UK, US and France Regulatory News: Lysogene (Paris:LYS) (FR0013233475 LYS), a phase 3 gene therapy platform company targeting central nervous system (CNS) diseases, today announced dosing of the first patient, at Royal Manchester Childrens Hospital, part of Manchester University NHS Foundation Trust, in the global adaptati...
United Kingdom United States Simon Jones Karen Aiach Manchester University European Union

Merck's KEYTRUDA® Given After Surgery Reduced the Risk of Disease Recurrence or Death by 32% Versus Placebo as Adjuvant Therapy in Patients With Renal Cell Carcinoma

KEYNOTE-564 is the First Phase 3 Study to Show Positive Results for Adjuvant Immunotherapy in RCC First-Time Disease-Free Survival Data to be Presented During Plenary Session at the 2021 ASCO Annual Meeting Merck known as MSD outside the United States and Canada, today announced first-time results from the pivotal Phase 3 KEYNOTE-564 trial evaluating KEYTRUDA, Merck’s anti-PD-1 therapy, for the potential adjuvant … KEYNOTE-564 is the First Phase 3 Study to Show Positive Results for Adjuvan...
United States Scot Ebbinghaus Tonik Choueiri Courtney Ronaldo Peter Dannenbaum Melissa Moody

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