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America’s biopharmaceutical companies are working around the clock to combat a common enemy: COVID-19. As the fight to research and develop innovative treatments and vaccines advances, I’m pleased to share our new TV ad, highlighting how we are working together to help end the global pandemic. Beginning today, the ad will appear on national cable and broadcast channels as well as online.

 

 

In the ad, three scientists detail how the biopharmaceutical industry is making progress to develop treatment and vaccine candidates against COVID-19 by collaborating in ways we’ve never done before.

 

We’ve made incredible progress in a matter of weeks, as we now have several vaccine candidates along with potential therapeutics that have shown positive results. Today, there are over 1,200 clinical trials for treatments and vaccines for COVID-19. Already, there are 13 vaccines in active clinical trials with over 120 in preclinical testing; these trials are occurring across 45 states and the District of Columbia.

 

In creating this ad, we’re proud to highlight several inspiring scientists that represent the more than 140,000 researchers across the country who are looking for vaccines, treatments and cures for coronavirus and other diseases. The three scientists in this ad also reflect the strong role women play in the life sciences industry, where women account for nearly half of the workforce up from just a third in 1990.

To learn more about biopharmaceutical efforts to combat coronavirus, visit PhRMA.org/Coronavirus.

Lori M. Reilly, Esq.

Lori M. Reilly is chief operating officer at PhRMA, providing executive level management, leadership and strategic direction for the organization. In this role, Reilly oversees PhRMA’s advocacy activities, including its federal, state and international government affairs and alliance development work. Reilly provides strategic leadership and works across PhRMA to develop and advocate for practical policy solutions that will lower costs for patients.

Reilly, named by the Washingtonian as one of the 250 most influential people in D.C., has a long record of working with members of Congress on a bipartisan basis and collaborating with stakeholders across the health care industry. Reilly is a frequent presenter on industry-related issues, including testifying before Congress on multiple occasions.

Reilly has over two decades of experience at PhRMA; prior to her current role, Reilly was the executive vice president of policy, research and membership at PhRMA, leading the development and implementation of legislative, regulatory and political strategies to advance policies that encourage patient access and medical innovation. She has also served as counsel at the U.S. House of Representatives Committee on Commerce and was Counsel to a member of the House Ways and Means Committee.

Reilly received a B.A. in political science from the University of Nebraska-Lincoln where she graduated with honors, and a J.D. from the University of Nebraska College of Law. She currently resides in Alexandria, Virginia with her husband and their four children.

Lori Reilly

https://x.com/lreilly71

https://www.linkedin.com/in/lorireillyphrma/

Chief Operating Officer

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Alzheimer's & Brain Awareness Month: A conversation with Eli Lilly and Company

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The use of real-world data in drug development

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Novel treatments and vaccines approved for U.S. patients in 2023 reach five-year high

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When it comes to the future of innovation, the ball is in policymakers’ court

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The White House continues to attack American innovation

December 15, 2023

Taking stock of obesity and its costly effects

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Congratulations to our 2023 Working for Cures Employee Champions

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Misuse of march-in could stifle innovation

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WHO Pandemic Agreement offers opportunities and risks for American innovators

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The IRA’s pill penalty threatens the future of oncology R&D

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Don't close the door on rare disease research

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Word of the Month: The Bayh-Dole Act

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WTAS on reasonable pricing and public-private partnerships

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Support for continued progress is critical for pediatric drug development

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New resource underscores the importance of small molecule medicines

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Policies need to address the growing threat of antimicrobial resistance

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World IP Day 2023: Celebrating women leaders in innovation

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CMS guidance on IRA price setting process doubles down on bad policy

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ICYMI: PhRMA President and CEO Stephen J. Ubl discusses patient affordability

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PhRMA provides comments and testimony to USITC investigation on COVID-19 medicines and the TRIPS Agreement

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PhRMA submits comments to OSTP on enhancing clinical trial diversity

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U.S. must address IP and market access barriers abroad to protect American innovation

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Novel medicines approved in 2022 offer increased treatment options for patients

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ICYMI: PhRMA kicks off the year at the 2023 J.P. Morgan Health Care Conference

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WTAS: Inflation Reduction Act already impacting R&D decisions

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Word of the Month: What is TRIPS?

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Expanding TRIPS waiver would jeopardize biopharmaceutical research and development

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TRIPS waiver expansion risks public health

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Congratulations to our 2022 Working for Cures Employee Champions

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New government price setting policy threatens post-approval research

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Expanding the WTO intellectual property waiver will hurt American jobs

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ICYMI: PhRMA COO Lori Reilly Esq. speaks with Jacob Van Naarden about the future of cancer research

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Protecting treatment advances for breast cancer

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Word of the Month: Long COVID

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New Report: Nearly 800 medicines in development to treat chronic conditions

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Partnerships are driving global COVID-19 treatment access

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The dangers of expanding the TRIPS waiver

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ICYMI: New research builds upon growing body of evidence on value of COVID-19 treatments and vaccines

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This week’s reading list: All the reasons the Senate-passed drug pricing bill is bad policy

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Myth vs. Fact: The Senate’s latest price setting proposal

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An open letter to Congress: Stand with patients and future cures

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ICYMI: A patient, physician, biotech investor and industry leaders warn about the dangers of government price setting bill

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PhRMA member companies’ R&D investments reach record high of $102.3 billion in 2021

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ICYMI: PhRMA’s Ubl pens op-ed on IP waiver for COVID-19 technologies

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Increase in drug-resistant superbugs during COVID-19 highlights need for policy reforms to address antimicrobial resistance

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Word of the Month: Biomarkers and surrogate endpoints

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ICYMI: Antimicrobial resistance spotlighted as growing public health threat

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CMS coverage decision restricts access to treatments for Alzheimer’s disease

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Biopharmaceutical researchers to discuss the value of R&D with Congress

June 9, 2022

Recognizing LGBTQ+ Pride in biopharmaceutical science

June 9, 2022

Intellectual Property waiver on COVID-19 innovation is unnecessary and harmful

May 23, 2022

Report: More than 500 medicines in development to treat disorders of the blood

May 18, 2022

ICYMI: PhRMA CEO Stephen J. Ubl spotlights lessons learned during COVID-19

May 13, 2022

Ensuring timely reauthorization of PDUFA and BsUFA

May 11, 2022

ICYMI: PhRMA COO Lori Reilly spotlights efforts to improve health care in 2022 and beyond

May 9, 2022

Spotlighting a growing mental health challenge

May 9, 2022

A conversation with Barry Greene, CEO of Sage Therapeutics

May 4, 2022

ICYMI: New resource catalogs biopharmaceutical industry lessons learned from COVID-19

April 28, 2022

Stephanie Dyson of BMS on reducing health disparities

April 27, 2022

The biopharmaceutical industry leads in helping women achieve new heights, according to IAM’s diversity 100

April 20, 2022

Report: More than 600 medicines in development for diseases affecting women

March 31, 2022

The accelerated approval pathway: Helping patients with serious or life-threatening diseases

March 17, 2022

Biopharmaceutical industry drives economic growth in all 50 states

March 14, 2022

Biopharmaceutical research and development has ushered in a decade of innovation in rare disease

February 28, 2022

4 things to know about biopharmaceutical efforts to fight cancer

February 24, 2022

New Data: COVID-19 vaccine global production capacity projected to exceed 20 billion doses this year

February 24, 2022

What you need to know about newly authorized COVID-19 antiviral treatments

February 22, 2022

Guest post: Joining forces to combat the COVID-19 mental health crisis

February 17, 2022

Guest Blog: COVID-19 vaccines are the key to keeping kids healthy

February 16, 2022

PhRMA submits comments urging CMS to withdraw coverage proposal

February 11, 2022

The importance of timely PDUFA and BsUFA reauthorization

February 3, 2022

Research and development continues long after a medicine is initially approved

February 1, 2022

Protecting U.S. innovation abroad to support economic and pandemic recovery

February 1, 2022

ICYMI: New approvals by the FDA in 2021 offer greater treatment options for patients

January 26, 2022

ICYMI: New report demonstrates growing global impact of antimicrobial resistance

January 24, 2022

New data show continued decline in death rates for cancer patients related to treatment advances

January 20, 2022

New Report: Nearly 800 new medicines in development to treat rare diseases

December 16, 2021

Recap: Our inaugural graduate summit and career expo

December 8, 2021

New report details the promise of the biopharmaceutical pipeline

December 7, 2021

3 things to know about the importance of post-approval research and development

December 6, 2021

Navigating the patient experience in the time of COVID-19

December 6, 2021

World AIDS Day: Remembering those we’ve lost and exploring the continued fight against HIV/AIDS

December 1, 2021

Global COVID-19 vaccination matters now and for the future

November 29, 2021

Guest post: Congress should not put future innovation at risk

November 29, 2021

Preventing the next public health emergency: New evidence demonstrates need to address antimicrobial resistance

November 18, 2021

Understanding breakthrough COVID-19 infections

November 11, 2021

New report highlights importance of IP-intensive manufacturing industries to the U.S. economy

November 1, 2021

PhRMA submission to 2022 National Trade Estimate Report underscores need for pro-innovation U.S. trade policy to combat COVID-19

October 29, 2021

Guest post: Continued research and development is critical for ALS patients and families

October 25, 2021

New report shows more than 260 medicines in development to fight neurodegenerative diseases

October 12, 2021

The important role of antivirals in the fight against COVID-19

October 6, 2021

Understanding Long COVID-19

September 29, 2021

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