ข่าวประชาสัมพันธ์ Daiichi Sankyo Company+Eli Lilly and Company

U.S. Regulators Approve Prasugrel for Reduction of Cardiovascular Events In Patients with Acute Coronary Syndromes Managed with Artery-Opening Procedure

Daiichi Sankyo Company, Inc. and Eli Lilly and Company (NYSE: LLY) today announced that the U.S. Food and Drug Administration (FDA) approved Effient(TM) (prasugrel) tablets for the reduction of thrombotic cardiovascular events (including stent thrombosis) in patients with acute coronary syndromes who are managed with an artery-opening procedure known as percutaneous coronary intervention (PCI). PCI usually includes the placement of a stent to help keep the artery open. Prasugrel works by

World Heart Federation, Daiichi Sankyo and Lilly Partner to Improve Cardiovascular Health

The World Heart Federation, Daiichi Sankyo Company, Limited (TSE: 4568) and Eli Lilly and Company (NYSE: LLY) announced today that they have partnered to improve cardiovascular health internationally. The...

European Commission Approves EFIENT(R) (prasugrel) for Patients with Acute Coronary Syndrome Undergoing PCI

Heart patients with acute coronary syndrome (ACS) undergoing an artery-opening procedure will soon have a new treatment option to help prevent heart attacks. Daiichi Sankyo Company, Limited ...

Prasugrel Receives Unanimous Approval Recommendation from FDA Advisory Committee

The U.S. Food and Drug Administration Cardiovascular and Renal Drugs Advisory Committee voted 9 to 0 that prasugrel, an investigational antiplatelet agent, should be approved for the treatment of patients with acute...

Triastek announces research collaboration with Lilly to explore the application of 3D printing technology in oral delivery of drugs

On July 13, 2022, Triastek, Inc. ("Triastek") announced a collaboration with Eli Lilly and Company ("Lilly"), a leading global pharmaceutical company, to leverage the...

New Data Show Lilly's Once-Weekly Trulicity(R) (dulaglutide) Solution for Injection is Effective as Add-on Treatment to Sulfonylurea

Trulicity 1.5 mg Demonstrates Superior Efficacy in AWARD-8 Trial New data from a completed Phase 3 trial show Trulicity(R) (dulaglutide) solution for injection 1.5 mg...

Detailed Results Demonstrate Baricitinib Superiority to Adalimumab in Improving Signs and Symptoms of Rheumatoid Arthritis

Once-daily oral baricitinib significantly improved all seven components of ACR response versus injectable adalimumab Patient-reported pain, joint stiffness, fatigue and physical...

European Commission Approves Trulicity(R) (dulaglutide) Solution for Injection, Lilly's Once-Weekly, Ready-to-Use Type 2 Diabetes Treatment

Trulicity, a glucagon-like peptide-1 (GLP-1) receptor agonist, is the only non-insulin, injectable diabetes treatment available in a pen with a no-see, no-handle...

Boehringer Ingelheim and Lilly Revising Operational Structure of Diabetes Alliance in Certain Countries

Significant portion of alliance opportunity will remain unchanged; some countries will transition to exclusive promotion in 2015 In a move that will strengthen their alliance by enhancing...

European Commission grants Lilly and Boehringer Ingelheim's insulin glargine product marketing authorisation in Europe

First biosimilar insulin to receive regulatory approval in the EU The European Commission (EC) granted marketing authorisation for Eli Lilly and Company and Boehringer Ingelheim's...

CHMP Recommends Lilly and Boehringer Ingelheim's New Insulin Glargine Product for Approval in the European Union

First biosimilar insulin to receive CHMP positive opinion in the EU The Committee for Medicinal Products for Human Use (CHMP) today issued a positive opinion recommending approval for the...

Studies Show Investigational New Insulin Glargine Product from Lilly and Boehringer Ingelheim Similar in Safety and Efficacy to Lantus(R)

Companies present comprehensive data for LY2963016, new insulin glargine product For the first time today, Eli Lilly and Company and Boehringer Ingelheim presented...

Lilly and Alzheimer's Disease International Partner to Address Barriers that Impact the Accurate and Timely Diagnosis of Alzheimer's Disease

New educational resources to help patients and caregivers communicate vital information with physicians are released as global leaders meet to discuss the...

Eli Lilly and Company and Boehringer Ingelheim announce new drug application filing in the U.S. for new insulin glargine product

New Drug Application follows submission of Marketing Authorisation Application to the European Medicines Agency Eli Lilly and Company and Boehringer Ingelheim today...

Lilly Releases Report on Corporate Responsibility Efforts

Company communicates progress on numerous indicators of economic, environmental, and social performance Eli Lilly and Company (NYSE: LLY) has released its 2012-13 Corporate Responsibility Report [http://www.lilly.com/Documents/Lilly_2012_2013...

Data Presented at 49th EASD Annual Meeting Show Treatment with Lilly's Investigational Dulaglutide Resulted in Improved Patient-Reported Health Outcomes

Improvements in several indicators of diabetes management, including perceptions about hyperglycaemia and weight, observed for investigational GLP-1...

Eli Lilly and Company and Boehringer Ingelheim announce regulatory submission for new insulin glargine biosimilar product

- European Medicines Agency accepted companies' marketing authorisation application Eli Lilly and Company (NYSE: LLY) and Boehringer Ingelheim today announced that the companies'...

Lilly Reassumes Sole Worldwide Development and Commercialization Rights for Novel Basal Insulin Analog

- Announces it will begin remainder of pre-planned clinical trials for LY2605541 Eli Lilly and Company (NYSE: LLY) and Boehringer Ingelheim International GmbH announced today they will adjust the...

ลิลลี่ เผยรายงานความคืบหน้าของการดำเนินการตามแนวทางความรับผิดชอบขององค์กร

บริษัทเปิดเผยถึงความคืบหน้าของปัจจัยบ่งชี้ทางเศรษฐกิจ สภาพแวดล้อม และการดำเนินการที่เกี่ยวกับสังคมหลายรายการ อิไล ลิลลี่ แอนด์ คอมพานี (Eli Lilly and Company) (NYSE: LLY) ได้เปิด...

CMC Biologics Announces Agreement With Daiichi Sankyo Company to Develop and Manufacture Antibodies

CMC Biologics today announced the execution of an agreement with Daiichi Sankyo Co., Ltd. ('Daiichi Sankyo') to provide process development support and manufacture of several clinical-stage antibodies...

สรุปข่าวเอเชียเน็ทประจำวันพฤหัสบดีที่ 17 กรกฎาคม 2551

ข้อตกลง โตเกียวและนิวเดลี: หลังจากที่มีการคาดการณ์กันมากในส่วนของสื่อมวลชนและตลาดหุ้น ไดอิจิ ซังเคียว จำกัด (Daiichi Sankyo Company, Limited) และ แรนแบ็กซี่ ลาบอราทอรีส์ จำกัด (Ranbaxy Laboratories Limited) ได้ตอกย้ำถึงข้อตกลงระหว่างกัน ...

AsiaNet Daily Summary - Press Releases for Thursday, July 17, 2008

BINDING DEAL... TOKYO and NEW DELHI: Following intense speculation in sections of the media and the stock market, Daiichi Sankyo Company, Limited and Ranbaxy Laboratories Limited reiterate that the agreement between Daiichi Sankyo,...

แรนแบ็กซี่ เตรียมดึง ไดอิจิ ซังเคียว เข้าถือหุ้นใหญ่ในบริษัท หวังขึ้นแท่นบริษัทเวชภัณฑ์ยักษ์ใหญ่ของโลก

บริษัท ไดอิจิ ซังเคียว จำกัด (Daiichi Sankyo Company, Limited) (TSE: 4568.JP) บริษัทเวชภัณฑ์รายใหญ่ที่สุดแห่งหนึ่งของญี่ปุ่น และ แรนแบ็กซี่ ลาบอราทอรีส์ จำกัด (Ranbaxy Laboratories Limited) (NSE/BSE...

Ranbaxy to Bring in Daiichi Sankyo as Majority Partner; Strategic Combination Creates Innovator and Generic Pharma Powerhouse

Daiichi Sankyo Company, Limited (TSE: 4568.JP) ("Daiichi Sankyo"), one of the largest pharmaceutical companies in Japan, and Ranbaxy Laboratories Limited (NSE/BSE: Ranbaxy...