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Interim Data from the heart-1 Phase 1b Clinical Trial of VERVE-101 in Patients with HeFH
Interim Data from the heart-1 Phase 1b Clinical Trial of VERVE-101 in Patients with HeFH

Interim Data from the heart-1 Phase 1b Clinical Trial of VERVE-101 in Patients with HeFH to be Presented at the American Heart Association (AHA) Scientific Sessions 2023 on November 12 at 3:30 p.m. ET; Company to Host Investor Event and Webcast on November 12 at 6:30 p.m. ET BOSTON, Nov. 07, 2023... Continue Reading

Date posted11/7/2023


Recor Medical and Otsuka Medical Devices Announce First FDA-Approved Renal Denervation System
Recor Medical and Otsuka Medical Devices Announce First FDA-Approved Renal Denervation System

Palo Alto, Calif. – November 7, 2023 – Recor Medical, Inc. (“Recor”) and its parent company, Otsuka Medical Devices Co., Ltd. (“Otsuka Medical Devices”) today announced the U.S. Food and Drug Administration (FDA) has approved Recor’s Paradise™... Continue Reading

Date posted11/7/2023


ASPC partners with Endless Health to support testing attendees’ cholesterol levels at family
ASPC partners with Endless Health to support testing attendees’ cholesterol levels at family

Dallas, TX. — The American Society for Preventive Cardiology (ASPC) together with Endless Health will be at the American Academy of Family Physicians’ (AAFP) annual conference – Family Medicine Experience (FMX) – in Chicago, IL October 27-29, 2023 – offering attendees... Continue Reading

Date posted10/23/2023


Novartis will appeal to U.S. Court of Appeals to uphold validity of Entresto® combination patent;
Novartis will appeal to U.S. Court of Appeals to uphold validity of Entresto® combination patent;

Basel, July 07, 2023 — Novartis today announced that the U.S. District Court for the District of Delaware issued a negative decision regarding the validity of a patent covering Entresto and combinations of sacubitril and valsartan, which expires in 2025 with its pediatric exclusivity.... Continue Reading

Date posted07/13/2023


US FDA approves expanded indication for Novartis Leqvio® (inclisiran) to include treatment of adults
US FDA approves expanded indication for Novartis Leqvio® (inclisiran) to include treatment of adults

EAST HANOVER, N.J., July 10, 2023 / PRNewswire / — Novartis announced today that the US Food and Drug Administration (FDA) has approved a label update for Leqvio® (inclisiran) to enable earlier use in patients with elevated LDL-C who have an increased risk of heart disease, as an adjunct... Continue Reading

Date posted07/13/2023


LEXICON ANNOUNCES FDA APPROVAL OF INPEFA™ (SOTAGLIFLOZIN) FOR TREATMENT OF HEART FAILURE
LEXICON ANNOUNCES FDA APPROVAL OF INPEFA™ (SOTAGLIFLOZIN) FOR TREATMENT OF HEART FAILURE

The Woodlands, Texas, May 26, 2023 – Lexicon Pharmaceuticals, Inc. (Nasdaq: LXRX) today announced that the U.S. Food and Drug Administration (FDA) has approved INPEFA™ (sotagliflozin), a once-daily oral tablet to reduce the risk of cardiovascular death, hospitalization for heart... Continue Reading

Date posted05/26/2023


ASPC and NLA publish joint clinical perspective on the importance of low-density lipoprotein
ASPC and NLA publish joint clinical perspective on the importance of low-density lipoprotein

Despite the established role of low-density lipoprotein cholesterol (LDL-C) as a major risk factor for cardiovascular disease (CVD), and the persistence of CVD as the leading cause of morbidity and mortality in the United States, national quality assurance metrics no longer include LDL-C... Continue Reading

Date posted02/28/2023