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Under Biden's Budget, These 2 Little-Known Biotechs Could Help End the Opioid Crisis


Jun 2, 2021 at 1:00PM
Among all of the overwhelming and depressing statistics associated with the coronavirus pandemic, here s one number that has sometimes been overlooked: 81,003 people in the U.S. died from drug overdoses in the 12-month period that ended in June 2020. That was a 20% year-over-year increase to a record high, due largely to a sharp surge in overdose deaths after COVID-19 struck. The combination of the added stressors of the pandemic and addicts inability to access support and treatment proved devastating to many. 
That s just one reason President Biden s recent budget proposal calls for $10.7 billion to fight the country s opioid addiction crisis. His proposal focuses on at-risk communities, and increases funding for everything from prevention to recovery programs. If the president gets his way, ....

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Heron Therapeutics to Present at the 2021 Jefferies Virtual Investor Conference


Heron Therapeutics to Present at the 2021 Jefferies Virtual Investor Conference
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SAN DIEGO, May 25, 2021 /PRNewswire/  Heron Therapeutics, Inc. (Nasdaq: HRTX), a commercial-stage biotechnology company focused on improving the lives of patients by developing best-in-class treatments to address some of the most important unmet patient needs, today announced that Barry Quart, Pharm.D., Chairman and Chief Executive Officer of Heron Therapeutics, will participate in a fireside chat at the 2021 Jefferies Virtual Healthcare Conference on Tuesday, June 1, 2021 at 11:00 am PT/2:00 pm ET.
A live webcast of the presentation will be available on the Company s website at www.herontx.com in the Investor Resources section. A replay of the presentation will be archived on the site for 60 days. ....

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Heron Therapeutics Announces U.S. FDA Approval of ZYNRELEF™ (HTX-011) for the Management of Postoperative Pain for up to 72 Hours


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SAN DIEGO, May 13, 2021 /PRNewswire/  Heron Therapeutics, Inc. (Nasdaq: HRTX), a commercial-stage biotechnology company focused on improving the lives of patients by developing best-in-class treatments to address some of the most important unmet patient needs, today announced that the U.S. Food and Drug Administration (FDA) has approved ZYNRELEF (bupivacaine and meloxicam) extended-release solution for use in adults for soft tissue or periarticular instillation to produce postsurgical analgesia for up to 72 hours after bunionectomy, open inguinal herniorrhaphy and total knee arthroplasty. ZYNRELEF, the first and only extended-release dual-acting local anesthetic (DALA), delivers a fixed-dose combination of the local anesthetic bupivacaine and a low dose of the nonsteroidal anti-inflammatory drug (NSAID) meloxicam. The synergy between bupivacaine and meloxicam in ZYNRELEF has resulted in patients experiencing significantly less pain, ....

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