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Search results for: drug prices

Possible Impact of Biosimilar Infliximab on U.S. Market in Prescriptions, Pricing

Kimberly Retzlaff  |  September 8, 2016

The use of biosimilars for rheuma­tology in the U.S. became a reality when the U.S. Food and Drug Administration (FDA) approved Inflectra (infliximab-dyyb), a biosimilar to Remicade (infliximab), in April. What this may mean is increased competition among drug companies with regard to pricing and, therefore, potentially lower costs for U.S. patients, according to Seoyoung…

Filed under:Biologics/DMARDsDrug Updates Tagged with:Biosimilarsdrug updateinfliximabprescriptionpricingrheumatologistrheumatology

The ACR Continues Fight to Block Medicare Part B Demo Project: Rule Expected in Fall 2016

Kathy Holliman  |  August 4, 2016

The ACR will seek Congressional action if the Medicare Part B demonstration project proposed by the Centers for Medicare & Medicaid Services (CMS) is not significantly altered by the agency. Today, Medicare Part B generally pays physicians and hospital outpatient departments the average sales price of a drug, plus a 6% add-on, minus reductions required…

Filed under:Legislation & AdvocacyProfessional Topics Tagged with:Centers for Medicare & Medicaid Services (CMS)Legislative Action CenterMedicare Part B

Biosimilars Debate Heats up over Cost Savings, Safety Concerns

Biosimilars Debate Heats up over Cost Savings, Safety Concerns

Susan Bernstein  |  April 15, 2016

After years of speculation about potential cost savings and debates on safety, biosimilars are about to step onto the stage of rheumatic disease treatment. On Feb. 9, the Arthritis Advisory Committee of the U.S. Food and Drug Administration (FDA) met in Washington, D.C., and recommended the approval of CT-P13, a proposed biosimilar to infliximab (Remicade),…

Filed under:Biologics/DMARDsDrug UpdatesLegislation & Advocacy Tagged with:BiologicsBiosimilarscost savingdebatedrugFDApatient careRheumatic DiseaserheumatologySafetyTreatment

The Biosimilars Debate Heats Up: Potential cost savings weighed against patient health & safety

Susan Bernstein  |  March 1, 2016

After years of speculation about potential cost savings and debates on safety, biosimilars are about to step onto the stage of rheumatic disease treatment. On Feb. 9, the Arthritis Advisory Committee of the U.S. Food and Drug Administration (FDA) met in Washington, D.C., and recommended the approval of CT-P13, a proposed biosimilar to infliximab (Remicade),…

Filed under:Biologics/DMARDsDrug Updates Tagged with:American College of Rheumatology (ACR)BiosimilarscostsFDAFood and Drug Administrationinfliximab

Market Turmoil Drives Small Biotechs to Big Pharma

Carl O'Donnell  |  February 19, 2016

(Reuters)—Numerous small biotechnology companies have been all but shut out of the capital markets, leaving many with no choice but to consider a sale to larger peers. The Nasdaq Biotech Index is down nearly 30% since September, when Democratic presidential candidate Hillary Clinton criticized drug companies’ “price gouging” on Twitter and sparked concerns about a…

Filed under:Uncategorized Tagged with:Biotechcostsdrugpharmaceutical company

Newly Released Documents Show Profit-Seeking Behind Price Hikes at Turing, Valeant

Sarah N. Lynch & Caroline Humer  |  February 3, 2016

WASHINGTON/NEW YORK (Reuters)—A decision by Turing Pharmaceuticals to raise the price of a lifesaving drug by 5,000% drove up some patient co-pays to as high as $16,000, according to excerpts of documents that congressional committee members released on Tuesday. The excerpts, which are highlighted in memos released by Democrats on the powerful U.S. House of…

Filed under:Drug Updates Tagged with:costsdaraprimdrug developmentDrugsTuring PharmaceuticalsValeant Pharmaceuticals

Looking Back on Rheumatology in 2015, Leaping Forward to the Year Ahead

Simon M. Helfgott, MD  |  December 16, 2015

My dear friends, we come to praise Caesar. As we march toward 2016, we ought to acknowledge the great Roman emperor’s role in creating a proper calendar. At the start of Caesar’s reign, the calendar year lasted 355 days, 10¼ days fewer than the time it took the earth to fully orbit the sun.1 Although…

Filed under:Legislation & AdvocacyOpinionPractice SupportProfessional TopicsRheuminationsSpeak Out Rheum Tagged with:Legislation & AdvocacyPractice ManagementProfessional TopicsRheuminations

Anthem to Buy Cigna to Create Biggest U.S. Health Insurer

Ankur Banerjee  |  July 24, 2015

(Reuters)—Anthem Inc. said on Friday it would buy Cigna Corp. in a deal valued at $54.2 billion, creating the largest U.S. health insurer by membership. The deal—the biggest ever in the health insurance industry—comes three weeks after Aetna Inc agreed to buy Humana Inc for $37 billion and is part of an industry-wide consolidation following…

Filed under:Drug Updates Tagged with:Anthem Inc.Cigna Corp.Health Insurance

After Default, Fight Breaks Out Over Greek Medicine Supplies

Ben Hirschler  |  July 6, 2015

LONDON (Reuters)—Wholesalers trading medicines across European borders have criticized a suggestion by manufacturers that Greek exports should be restricted to prevent shortages of life-saving drugs in the country. Such trade, which allows traders to buy products in low-cost markets and sell them where prices are higher, is allowed under EU free trade rules. But drugmakers…

Filed under:Drug Updates

Greece’s Medicine Supply May Be in Jeopardy

Ben Hirschler  |  June 29, 2015

BASEL, Switzerland (Reuters)—Drugmakers said on Monday they would continue to ship medicines to Greece in coming weeks, despite mounting unpaid bills, but warned supplies could be in jeopardy if Europe did not take emergency action. “In the worst-case scenario of ‘Grexit’, we believe the integrity of the medicines supply chain may be in jeopardy, which…

Filed under:Drug Updates Tagged with:Drug shortageEuropean UnionGreece

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