Policy & Regulation: Page 11


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    Samara Heisz via Getty Images
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    Eli Lilly took price cuts into its own hands. Will other pharmas follow suit?

    The pharma giant took the high road and cut prices before the feds made them. How will that affect the industry?

    By March 7, 2023
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    FDA ups generics and biosimilar approvals for a shot at lower drug costs

    As the Biden administration searched for drug-cost reducing measures, the FDA incentivized generic and biosimilar development in 2022. 

    By Karissa Waddick • March 6, 2023
  • rare disease ribbon Explore the Trendline
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    Trendline

    Rare diseases

    As drug developers find promise in the rare diseases, deals and treatments are on the rise

    By PharmaVoice staff
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    Multimillion-dollar therapies are changing how payers foot the bill

    With more gene therapies headed to market, novel payment methods are emerging from regulators and academia. 

    By Feb. 28, 2023
  • Who is Vivek Ramaswamy — the biotech entrepreneur turned presidential candidate?

    The former CEO of Roivant, who became the face of the “anti-woke” business movement, is now running for the 2024 Republican presidential nomination. Here’s what he stands for. 

    By Karissa Waddick • Feb. 27, 2023
  • Faby Malik Cytokinetics
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    Permission granted by Dr. Faby Malik, Cytokinetics
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    Q&A // Biotech Spotlight

    Cytokinetics looks to muscle into the cardiovascular market

    With a scientific platform based on muscle biology, the late-stage biotech is addressing cardiovascular and neuromuscular diseases.

    By Feb. 24, 2023
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    Why FDA’s approach to orphan drug exclusivity is ripe for more legal challenges

    Despite a court ruling, the FDA is sticking to its narrow orphan drug exclusivity approach. But confusion remains over the policy’s future. 

    By Karissa Waddick • Feb. 23, 2023
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    Win McNamee / Staff via Getty Images
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    Marking one year as FDA commissioner, Califf lays out vision for agency’s future

    Califf outlined hopes to address advisory committees, drug pricing, digital health and more.

    By Karissa Waddick • Feb. 16, 2023
  • Kinnari Patel Rocket Pharmaceuticals
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    Permission granted by Kinnari Patel Rocket Pharmaceuticals
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    Q&A

    Rocket Pharmaceuticals is ready for liftoff in the rare disease space

    With two rare disease products on the launch pad for FDA submission in 2023 and a growing pipeline, Rocket is fueled for its next era of growth.

    By Feb. 10, 2023
  • FDA commissioner testifying to Congress
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    Kevin Dietsch via Getty Images
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    3 ways the FDA’s restructuring plan could impact pharma

    FDA’s food program is in for a major overhaul — here’s why pharma should pay attention. 

    By Karissa Waddick • Feb. 9, 2023
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    Permission granted by Alexion
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    Profile

    United by inequity: The healthcare disparities plaguing rare disease patients and Black Americans

    Guided by her personal experiences, Tamar Thompson is aiming to improve rare disease care through her advocacy work at Alexion, AstraZeneca Rare Disease.

    By Alexandra Pecci • Feb. 7, 2023
  • Roche Pharmaceutical Group's office building in Shanghai, China
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    iStock via Getty Images
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    Making Moves

    Roche, Chiesi and the FDA change major leadership roles as they strive for growth in 2023

    From Roche’s new pharma chief to the departure of the FDA’s gene therapy head, these moves are bound to shake up the industry.

    By Karissa Waddick • Feb. 6, 2023
  • The Federal Trade Commission headquarters is pictured in Washington, D.C. The agency's proposed noncompete ban may face legal challenges on several grounds.
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    RiverNorthPhotography via Getty Images
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    Antitrust watchdogs have pharma in their sights, and the landscape is getting thornier

    The FTC and DOJ are heightening antitrust enforcement, and pharma deals are a prime target.

    By Karissa Waddick • Feb. 2, 2023
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    Vaxxinity eyes global COVID-19 vaccine market with ‘next-gen’ booster

    The biotech aims to complete rolling submissions with regulators in the U.K. and Australia in the first half of 2023.

    By Alexandra Pecci • Jan. 31, 2023
  • A prescription bottle with white pills and a wooden gavel sit atop a $100 bill showing Benjamin Franklin's face.
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    Bill Oxford via Getty Images
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    Drug price negotiations: 5 key dates to watch

    As the CMS readies its new program for lowering drug costs, these are the moments that will matter most to pharma companies.

    By Kelly Bilodeau • Jan. 23, 2023
  • The headquarters of the FDA, which has recently issued a recall for Teleflex air filters used in hospital respirators.
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    Sarah Silbiger/Getty Images via Getty Images
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    FDA’s 2022 drug approvals fall short of recent norms

    The U.S. agency’s lower number of novel drug approvals followed several controversies surrounding a 2021 Alzheimer’s approval.

    By Alexandra Pecci • Jan. 19, 2023
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    Carsten Koall via Getty Images
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    After ‘limping along,’ Novavax sees a path forward

    With a new CEO and a long-term booster strategy, the company believes there’s plenty of room to grow in the COVID-19 vaccine space.

    By Jan. 18, 2023
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    Cemile Bingol via Getty Images
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    Lilly, Biogen, Eisai brace for Alzheimer’s boom or bust in 2023

    As controversies abound and new drugs rise on the regulatory horizon, this year will be big for Alzheimer’s.

    By Jan. 5, 2023
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    Opinion

    The 2023 PharmaVoice Crystal Ball: Peering into the future of life sciences

    A preview of the top trends on the minds of industry and market leaders for the new year.

    By Jan. 3, 2023
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    Illustration: Alberto Miranda for Industry Dive

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    Tracker

    The 2023 PharmaVoice Year in Preview

    Here’s a look at how industry leaders are navigating the key issues of 2023.

    Dec. 12, 2022
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    Courtesy of Sarepta
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    Q&A

    For Duchenne-focused Sarepta, gene therapy is the natural next step

    The company with three marketed RNA drugs for Duchenne muscular dystrophy is taking the logical leap into gene therapies with a candidate under review at the FDA.

    By Dec. 8, 2022
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    Permission granted by CSL
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    Q&A

    A historic approval could transform CSL from being ‘the biggest company no one has ever heard of’

    The company’s head of R&D on its profile-raising FDA approval of a gene therapy that’s now the world’s most expensive drug. 

    By Dec. 6, 2022
  • The front entrance of the Food And Drug Administration headquarters building.
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    Sarah Silbiger via Getty Images
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    An FDA proposal could make OTC switches easier. Here’s what the industry has to say

    How the FDA’s proposal to create a new OTC approval pathway could impact the pharma industry.

    By Karissa Waddick • Dec. 5, 2022
  • A sign for the Food And Drug Administration is seen outside of the headquarters on July 20, 2020, in White Oak, Maryland.
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    Sarah Silbiger via Getty Images
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    5 final FDA action dates to watch this year

    A potential flurry of regulatory activity could be on the horizon yet this year — and several key drug approvals are at stake.

    By Dec. 1, 2022
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    10 of our most popular articles in 2022

    Methadone, rock ‘n’ roll, clinical trial overhauls — here’s a look at our most-read stories of the year.

    By Nov. 30, 2022
  • A view of a sign that reads, "Kendall square: central square, Harvard square, cinema" is framed by a pill outline.
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    Photo illustration: Shaun Lucas and Karissa Waddick/Industry Dive; Getty Images 

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    The next era of Greater Boston’s biotech boom

    How Boston became the biotech capital of the U.S., and is now preparing for the next era of life sciences growth.  

    By Karissa Waddick , , Nov. 22, 2022