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Health Advisory Council Newsletter | Fall 2020

Member updates

America’s Health Insurance Plans (AHIP)

Association for Accessible Medicines (AAM)

BeMedWise at NeedyMeds

Brian Isetts, University of Minnesota College of Pharmacy

Council for Affordable Health Coverage (CAHC)

Deterra System

Eli Lilly and Company

Food and Drug Administration (FDA) Office of Women’s Health

Healthcare Distribution Alliance (HDA)

National Association of Nurse Practitioners in Women’s Health (NPWH)

Pharmaceutical Research and Manufacturers of America (PhRMA)

America’s Health Insurance Plans (AHIP)

As our nation works to overcome the COVID-19 crisis, health insurance providers continue to take decisive action to ensure that Americans have access to the prevention, testing, and treatment they need. In addition to COVID-19, health insurance providers are on the frontlines in the *response to ongoing wildfires and hurricane activity across the country. Their efforts reflect the ongoing commitment to ensure the safety and health of all Americans.

Health insurance providers are also taking steps to increase vaccination rates for adults and children amid the pandemic. AHIP created a flu vaccine toolkit including an *infographic detailing the value of the vaccine, which can reduce the risk of a flu-related intensive-care admission by 82% among adults. Additionally, the Modern Medicaid Alliance, of which AHIP is a founding member, promoted partners’ vaccine resources in honor of National Immunization Awareness Month. AHIP and our coalitions will continue to highlight the importance of seasonal and routine vaccinations.

The Modern Medicaid Alliance updated its Medicaid Dashboard, a one-stop clearinghouse for Medicaid enrollment and polling data at the national and state levels. According to recent polling housed on the Dashboard, 86 percent of adults want a strong, sustainable Medicaid program, and over two-thirds of adults in key swing states (AZ, FL, MI, PA, WI) oppose cutting funding for Medicaid. The Alliance continues to use the Dashboard and other tools to advocate for increased funding for Medicaid amid the COVID-19 crisis, including a partner sign-on letter to Congressional leadership, polling research, and an infographic outlining the consequences of Congressional inaction to increase states’ federal medical assistance percentage (FMAP).

To learn more about health insurance providers actions to support Americans amid the COVID-19 crisis, AHIP, or the Modern Medicaid Alliance, contact Nicole Eynard at neynard@ahip.org

Association for Accessible Medicines (AAM)

The Association for Accessible Medicines (AAM) recently released the *2020 Access & Savings Report detailing the economic benefit of generic and biosimilar drugs to America’s patients. According to the report, the U.S. health care system saved $313 billion in 2019 from generics and biosimilar drugs, including $96 billion in Medicare savings and $48.5 billion in savings to Medicaid. At a time when access to reliable, affordable, and high-quality prescription medication is more important than ever, generics fill 90 percent of prescriptions in the United States for only 20 percent of the cost. The findings reinforce the outsized importance of the generic industry in delivering lifesaving and health-managing medicines to patients. The title of this year’s report, Securing Our Access & Savings, reflects widespread stakeholder concerns about the availability of essential medicine during the pandemic, and the resilience of the industry in managing the global supply chain to deliver drugs without significant disruption.

Additionally, in August, AAM’s Board of Directors announced the appointment of Dan Leonard to be the association’s President and Chief Executive Officer starting in September. He most recently served as President and Chief Executive Officer of the National Pharmaceutical Council (NPC), and succeeds Chester “Chip” Davis, Jr. who left AAM in February 2020.

BeMedWise at NeedyMeds

This October, the BeMedWise Program at NeedyMeds celebrates 35 years of “Talk About Your Medicines” Month (TAYMM). Talk About Your Medicines, a well-recognized health observance month has grown and expanded over three decades to stimulate conversations between patients, caregivers, and their healthcare providers about all the types of medicines they may take, with a focus on what to know about a medication in terms of expected health outcomes, possible side effects, benefits, and potential risks. The 2020 TAYMM theme is Medication Adherence – On Track with Your Meds and Your Health. Please click here to view the Press Release and the Oct. 1 kick-off TAYMM webinar. The TAYMM messages are evergreen and Talk About Your Medicines.org features downloadable handouts, social media, and a comprehensive educational resource library featuring the many initiatives of the BeMedWise Council Supporters and Partners.

On September 10, BeMedWise held a virtual stakeholder meeting for the BeMedWise Council Supporters. During the meeting, participants listened to NeedyMeds President Rich Sagall, MD, Carla Dellaporta, Director of User Engagement, NeedyMeds, and Deborah Davidson, BeMedWise Director of Special Projects provide a preview of this year’s Talk About Your Medicines Month activities and highlighted partnership opportunities. On October 1, Deborah participated in a panel discussion: Reaching Older Adults with Safety Messaging as part of the Johnson and Johnson Consumer Inc., PartnerLink virtual meeting. On October 29, NeedyMeds will host the National Consumers League webinar: “FakeRx: Counterfeit Drugs in the Era of COVID-19” as part of NCL’s FakeRx initiative.

To learn more about how you can get involved in BeMedWise, including opportunities to collaborate on educational program development, webinars and TAYMM, contact Deborah.Davidson@needymeds.org. 

Brian Isetts, University of Minnesota College of Pharmacy

Brian Isetts served as an expert panelist for a national Webinar on September 22nd titled, Looming Challenges of COVID-19 Immunization: Preparing the Immunization Infrastructure, hosted by the Network for Excellence in Health Innovation. Watch their vaccine Summit series *here.

Council for Affordable Health Coverage (CAHC)

During the current COVID-19 pandemic, the Council for Affordable Health Coverage (CAHC) continues to fight for policies that ensure health coverage remains affordable. Our 2020 priorities and activities are outlined below:

  • Value/Outcomes-Based Arrangements: The Council for Affordable Health Coverage (CAHC) has continued pushing to expand access to Value-Based Arrangements (VBAs) in federal and private health programs, most recently through our new campaign: A Campaign for Transformative Therapies (CTT), which is advocating for legislation that will enable VBAs for gene therapies.
  • COBRA subsidies: In response to the pandemic, CAHC supports premium assistance for the continuation of private coverage as a way to help those who lose their jobs or who are furloughed. While there has been legislation introduced, we believe it needs work and have partnered with American Benefits Coalition and ERIC to ensure the problems are resolved and the bill is passed.
  • Surprise Billing: Surprise medical billing is a continued focus as uncertainties about coverage of COVID testing and treatment remain, and patients may be navigating new insurance networks. CAHC continues to work with Congressional committees and stakeholders to come to an agreement and pass legislation banning surprise billing.
  • HealthCosts: CAHC’s parent company recently completed a report on the state of the health care system and health cost drivers in the state of North Dakota. The report, done in collaboration with the North Dakota Insurance Commissioner’s office, is a window into what’s increasing the cost of health care in the state over the past several years.
  • CAHC in the News: CAHC President Joel White has been quoted in a slew of articles in the New York Times, on issues ranging from the upcoming *Supreme Court confirmation battle to the *President’s executive orders.

Deterra System

Deterra System would like to share the details of our partnership with SAFE Project, a national nonprofit working to end the addiction epidemic, and the fall Gone for Good® at-home medication disposal campaign which launched earlier this month.

This past spring, we launched our first ever Gone for Good campaign and gave away 10,000 Deterra® Drug Deactivation Pouches nationwide, nearly double our goal. And now we are ready to do it again and you can help! Throughout October, anyone can sign up to get a FREE Deterra Pouch shipped to their home by visiting DeterraSystem.com/SAFE. Please encourage your friends, family, organizations, neighbors, etc. to request a Pouch and use these marketing resources to spread the word!

  • Social, email, newsletter assets
  • SAFE project press release
  • Admiral Winnefeld PSA

We welcome the Health Advisory Council to help get the word out! See below for the newsletter copy and above for the Social, Email, Newsletter Assets.

***

NEWSLETTER COPY:

[headline] Ensure Unused Medications are Gone for Good

[subhead] SAFE Project has partnered with Deterra to provide free at-home drug disposal

October 1 – 31, SAFE Project and the creators of the Deterra® Drug Deactivation System are teaming up to bring at-home drug disposal to households across the US – for free. With access to take back sites limited during COVID-19, people can go online and request a Large Deterra Pouch to deactivate unused prescription or over-the-counter medications permanently and safely from the comfort of their home.

Help us stop the cycle of drug abuse, misuse, and diversion: request your Deterra Pouch at DeterraSystem.com/SAFE and spread the word on social media using #GoneForGoodUS.

Eli Lilly and Company

Lilly has launched “Insulin Affordability: Learn. Act. Share.” to encourage those who use Lilly insulin to:

  • Learn about our affordability options
  • Act by visiting insulinaffordability.com or calling the Lilly Diabetes Solution Center
  • Share this important information with others who may benefit from our solutions.

Lilly’s suite of solutions includes the Lilly Insulin Value Program, which reduces the out-of-pocket cost for most Lilly insulins to $35 per monthly prescription. People without insurance, as well as those with commercial insurance, are eligible for the savings.

Beginning in January 2021, people enrolled in participating Medicare Part D insurance plans will be able to access their Lilly insulin for $35 per monthly prescription as part of the Medicare Part D Senior Savings Model. It is important that seniors enroll in a participating Medicare Part D plan that covers their insulin this fall during open enrollment. That is why Lilly has created a resource at insulinaffordability.com, where users can enter their zip code and view which Medicare plans are participating and covering Lilly insulins.

Additionally, representatives at the Lilly Diabetes Solution Center can help identify which affordability options best meet the specific needs of individual callers, including information about how to access donated Lilly insulin for those who qualify.

“It’s important that people are aware of our insulin affordability options – and take action – to benefit from them. With this campaign, we hope to ensure people living with diabetes know their options and are empowered to access them through the Lilly Diabetes Solution Center,” said Andy Vicari, Lilly’s U.S. insulins brand leader.

To learn more, visit insulinaffordability.com or call the Lilly Diabetes Solution Center Monday – Friday from 8am – 8pm EST at (833) 808-1234 to speak with a live representative. Representatives can help people in just a few minutes, and translations are available in numerous languages.

Food and Drug Administration (FDA) Office of Women’s Health

The FDA Office of Women’s Health (OWH) is hosting a public meeting to discuss potential sex (biological) and gender (psychosocial) differences in use and responses to cannabidiol (CBD) and other cannabinoids. Researchers, educators, clinicians, and patients may benefit from attending this multidisciplinary scientific conference on CBD and other cannabinoids. All are encouraged to register for the conference here.

Additionally, during Women’s health week, OWH launched a new blog titled Knowledge and News on Women, abbreviated as KNOW. This first blog topic focused on women prioritizing physical, and mental health, while navigating the challenges presented by the COVID-19 pandemic. During Fibroid Awareness Month in July, the OWH blog helped shed light on uterine fibroids and highlighted FDA’s recent approval of the first medical treatment option – an oral medication – specifically for reducing heavy menstrual bleeding caused by uterine fibroids, a condition that may women often suffer with silently. The blog also featured testimonials from key stakeholders dedicated to raising awareness of uterine fibroids given their personal experiences.

Links to the OWH blog are in the navigation tab on our homepage and can also be accessed directly. The FDA OWH Associate Commissioner, Dr. Kaveeta Vasisht, was also featured on FDA’s Insight podcast this week, sharing the latest on OWH’s women’s health activities. The full interview is available *here.

Healthcare Distribution Alliance (HDA)

The Healthcare Distribution Alliance (HDA) and its members continue to support COVID-19 response efforts. Recently, HDA released a series of *principles for vaccine distribution that reaffirm the pharmaceutical distribution industry’s commitment to ensuring — in partnership with federal and state governments — the safe and efficient distribution of COVID-19 vaccines once they are approved by the Food and Drug Administration. The principles highlight utilizing the industry’s network and expertise, securing the vaccine supply, working with federal and state governments, and practicing transparency and communication.

Additionally, HDA is sponsoring an event with The Hill on October 27th from 1-2 p.m. that examines the supply chain’s response to COVID-19 and discusses how it is preparing for the next phase of this global pandemic. For more information about the event or HDA’s activities please contact Farah Simonett at fsimonett@hda.org.

National Association of Nurse Practitioners in Women’s Health (NPWH)

NPWH White Paper: The Essential Role of Women’s Health Nurse Practitioners

The NPWH White Paper: The Essential Role of Women’s Health Nurse Practitioners provides details and clarification on the unique aspects of WHNP education, competencies, certification, roles on the healthcare team, and some specialized areas of practice for which WHNPs are distinctly prepared. The audience for this white paper includes a variety of stakeholders in women’s health that include, but are not limited to prospective and current WHNP students, practicing WHNPs, other members of the healthcare team, schools of nursing and NP faculty, employers, and consumers of women’s healthcare services.

NPWH affirms the essential role of WHNPs as members of the women’s healthcare team. In this white paper, we describe strategies to address challenges and to ensure a robust future for the role of the WHNP. We hope you will take the time to read the white paper and join us in active support of the WHNP role. *Please share the white paper (PDF) during conversations with nurse colleagues and student nurses who have a passion for women’s health. Tell them about the personal and professional rewards you have experienced as a WHNP.

NPWH Position Statement: *The Doctor of Nursing Practice for Women’s Health Nurse Practitioners.

The National Association of Nurse Practitioners in Women’s Health (NPWH) supports a pragmatic approach to the continuing evolution of the Doctor of Nursing Practice (DNP) degree as entry-level for women’s health nurse practitioners (WHNPs). During the transition, study of the impact of DNP education on quality, access, and cost of healthcare should be ongoing. Policies must be in place to ensure that currently practicing WHNPs are not disenfranchised from practice in any way. Furthermore, NPWH advocates for concerted strategies to maintain an adequate number of highly qualified WHNPs to meet the healthcare needs of individuals and communities.

Pharmaceutical Research and Manufacturers of America (PhRMA)

At PhRMA, we continue to have meaningful conversations about diversity & inclusion with internal voices on our PhRMA.org/Equity site and with external thought leaders, like Dr. Freda Lewis-Hall in The Washington Post. We are also pushing back against policies that threaten diversity & inclusion and work towards enhancing the country’s STEM education programs, creating a diverse talent pipeline with the next generation of scientists, engineers and technology professionals. Our industry will continue to fight inequality and look forward to seeing what the next several months hold for us as biopharmaceutical companies continue this work. Our industry will continue to fight for equity. Follow our progress at PhRMA.org/Equity.

*Links are no longer active as the original sources have removed the content, sometimes due to federal website changes or restructurings.

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PBPA Commends HHS Funding to Support Maternal and Infant Health

The Preterm Birth Prevention Alliance (PBPA), a coalition of maternal and women’s health advocates dedicated to improving preterm birth outcomes in the United States and addressing its disproportionate impact on women of color, applauds the U.S. Department of Health and Human Services (HHS) for awarding nearly $350 million to states across the country to improve support for safe pregnancies and healthy babies.

“For far too long, U.S. maternal health care has lagged behind that of other developed countries, particularly for women of color,” noted Sally Greenberg, Executive Director of the National Consumers League. “This additional funding will enable local health departments and nonprofits to better address the health care needs of the most vulnerable mothers and their babies.”

The funding, awarded by HHS’ Health Resources and Services Administration (HRSA), will support home visiting services, increase access to doulas, address infant mortality and maternal illness, and improve data reporting on maternal mortality.

“Maternal health care in the U.S. has consistently failed women of color,” Greenberg continued.  “We applaud HHS for this additional funding that will help to improve the maternal health for all mothers and babies, especially women of color and those most at-risk.”

The funding announcement follows the release of a report by the U.S. Commission on Civil Rights which found that Native American women are more than two times more likely to die from pregnancy-related complications than white women in the U.S. This disparity was further exacerbated for Black women in the U.S., who are three to four times more likely to die from pregnancy-related complications than white women.

“In addition to expanding programs to support maternal health, we must increase representation from racially and ethnically diverse groups in research and clinical trials, particularly those studying treatment options to prevent maternal morbidity and mortality,” said Greenberg.  “The need for the additional HHS funding and the report from the Commission on Civil Rights clearly illustrate how critical representative research and real world evidence are to ensuring all mothers and their babies have the same opportunity for the best possible health outcomes.”

Diverse research for a diverse America: The value of equitable, real-world research

August 12, 2021/in Blog, Health, Prevention Blog Post

By Sally Greenberg, NCL Executive Director

While the COVID-19 pandemic has led to hardship for all Americans, it is clear that people of color have been disproportionately burdened. Across the health care continuum, addressing this disparity has become part of the broader conversation about the history of systemic racism and the underlying social determinants of health that negatively affect the mental, physical, and economic health of individuals and entire communities.

The pandemic has underscored persistent health disparities, and there is growing recognition that representation in research and clinical trials can have a profound impact on health outcomes. A lack of representation from racially and ethnically diverse groups in research and clinical trials have typically led to gaps in data, missing the opportunity to assess the full impact of various treatments and drugs across a range of populations. The collection and use of real-world research and data to inform the potential use, risks, and benefits of medical products and treatments can ultimately lead to better health outcomes, particularly for those who have been underrepresented in the past.

Existing efforts to improve inclusion

Efforts to expand diversity and representation in medical research are underway in Congress. Policymakers are encouraging the incorporation of Real World Evidence (RWE) in drug development through the recent Cures 2.0 draft legislation released by Reps. Diana Degette (D-CO-1) and Fred Upton (D-MI-6). While the status quo limits us from effectively reaching underserved populations, the proposed legislation would allow studies that include RWE for some drugs after they have been approved. At the heart of this issue is a growing appreciation that the same therapy can affect different populations in different ways, which is why Cures 2.0 supports collecting data that more accurately reflects the unique experiences and needs of patients across diverse populations.

Recognizing the potential for RWE in maternal health

The lack of representative research in the field of maternal health is undeniable, and its implications are staggering. The dismal state of maternal care in the United States reflects how our health care system has failed women of color, including by not adequately studying treatment options to prevent maternal morbidity and mortality. The need for RWE is clear when you consider the persistent disparities in health outcomes that plague minority communities.

Preterm birth and its disproportionate impact on women of color is a stark illustration of the need to make progress on representative research in maternal health. Preterm birth is the second-largest contributor to infant death in America today. Despite the tremendous physical, emotional, and financial toll that preterm birth continues to take on our country — disproportionately so on women and families of color — not enough therapeutic tools currently exist to prevent it.

Today, “17P,” the only FDA-approved treatment to help reduce the likelihood of spontaneous, recurrent preterm birth in the United States is at-risk of being withdrawn from the market in all its forms, including the branded product and five generic versions. Unfortunately there is conflicting evidence from two different clinical trials, one representative of a diverse U.S. population and another studied in a largely white population in Europe. It’s not a straightforward comparison. If 17P is withdrawn, the women most affected by preterm birth, predominantly women of color, would be left without an FDA-approved treatment option.

The FDA is considering the path forward, including additional data collection through leveraging RWE from past patient use. The success of the first (approval) trial for 17P in the impacted communities signals the importance of RWE. Continued access to 17P is, at its core, a matter of health equity. Black women must not yet again be left vulnerable to a system that historically has overlooked them.

PRETERM BIRTH PREVENTION ALLIANCE APPLAUDS FDA’S GRANTING OF HEARING FOR THE ONLY FDA-APPROVED THERAPIES TO REDUCE RECURRENT PRETERM BIRTH

WASHINGTON, DC, August 26, 2021 –

Preterm Birth Prevention Alliance a coalition of maternal and women’s health advocates dedicated to improving preterm birth outcomes in the United States and addressing its disproportionate impact on women of color, commends the U.S. Food and Drug Administration (FDA) for granting a public hearing to discuss 17P, the only FDA-approved class of branded and generic treatments to reduce preterm birth in indicated patients.

We appreciate the FDA’s willingness to hear directly from individuals facing prematurity and the providers who treat them about their experiences with 17P,” said National Consumer League’s Executive Director Sally Greenberg. “It is an important step towards better understanding variations in efficacy across diverse populations and ensuring all women have an equal chance at the best possible outcomes.”

Last week, the FDA agreed to grant Covis Pharma, the manufacturer of the branded 17P product Makena its request for a public hearing to discuss 17P. Hydroxyprogesterone caproate—or “17P”—has been approved since 2011 and is the only FDA-approved class of treatments to help prevent spontaneous, recurrent preterm birth in the United States. In 2020, the FDA proposed withdrawing 17P in all its forms, including the branded product and its five generic versions, based on conflicting efficacy data from two studies composed of vastly different populations, one predominantly inclusive of women in the U.S. most vulnerable to preterm birth and one not.

“Mothers and birthing people deserve access to the best possible treatments to prevent preterm birth. We cannot achieve birth equity if we study pregnant women as a monolith,” said Blythe Thomas, Initiative Director of 1,000 Days. “It is only by systematically researching the real-world, post-market impact of 17P on individuals from a variety of racial and ethnic backgrounds, while maintaining access for all affected, that we can reduce disparities in maternal and infant health.”

While the hearing date has not yet been set, the Alliance looks forward to sharing the perspectives of affected individuals and their physicians with the agency once the hearing is scheduled and will continue to advocate for at-risk moms and babies of all races and ethnicities.

###

ABOUT THE PRETERM BIRTH PREVENTION ALLIANCE

The Preterm Birth Prevention Alliance (PBPA) is a coalition of maternal and women’s health advocates who share a common concern about the state of preterm birth in the United States and the proposed market withdrawal of 17P, the only FDA-approved class of treatments to help prevent spontaneous, recurrent preterm birth. Formed in 2021 by the National Consumers League, the 15 partners in the PBPA seek to improve preterm birth outcomes in the United States by maintaining access to safe, FDA-approved treatment options and advocating for more diverse medical research that adequately represents the experiences of women and newborns of color. Women of color need a seat at the table. To learn more, visit www.pretermbirthalliance.org

LEADING PATIENT ADVOCATES LAUNCH PRETERM BIRTH PREVENTION ALLIANCE TO PROTECT CRITICAL ACCESS TO THE SOLE FDA-APPROVED CLASS OF THERAPIES TO REDUCE RECURRENT PRETERM BIRTH

WASHINGTON, DC, April 20, 2021 – Today, the National Consumers League (NCL), along with a coalition of patient advocacy organizations dedicated to advancing the health of mothers and infants, announced the launch of the >Preterm Birth Prevention Alliance.

Members of the Alliance are joining forces in an effort to preserve patient access to the only Food & Drug Administration-approved class of treatments for pregnant women who have previously had an unexpected, or spontaneous, preterm birth. Together, Alliance members seek to ensure that the Food & Drug Administration (FDA) hears concerns from the full range of stakeholders about the potential risks and impact of withdrawal for at-risk pregnant women and their providers.

For the fifth year in a row, the U.S. preterm birth rate has increased (to 10.2 percent of births), and preterm birth and its complications were the second largest contributor to infant death across the country. Preterm birth also represents a significant racial health disparity, with Black women in America experiencing premature delivery at a rate 50 percent higher than other racial groups throughout the country.

However, in 2020, the FDA >proposed withdrawing hydroxyprogesterone caproate, commonly called “17P” or “17-OHPC”, the only FDA-approved class of branded and generic treatments to help prevent the risk of preterm birth in women with a history of spontaneous preterm birth. The FDA is currently determining whether to hold a hearing on the status of 17P, based on conflicting efficacy data from two studies composed of vastly different patient populations, one inclusive of women in the U.S. most vulnerable to preterm birth and one not.

“We’re fighting for a more inclusive healthcare system that gives everyone an equal chance to have the best outcomes possible,” said Sally Greenberg, executive director of the National Consumers League. “We don’t believe that removing 17P from the market without gaining a better understanding of who could benefit the most from its use is in the best interests of patients, nor their healthcare providers, particularly as there are no other approved treatment options available.”

To date, 14 organizations have joined NCL to advocate for the health interests of at-risk pregnant women and infants, including: 1,000 Days; 2020 Mom; American Association of Birth Centers; Black Mamas Matter Alliance; Black Women’s Health Imperative; Expecting Health; Healthy Mothers, Healthy Babies Montana; HealthyWomen; Miracle Babies; National Birth Equity Collaborative; National Black Midwives Alliance; National Partnership for Women & Families; Sidelines High-Risk National Support Network; and SisterReach.

“As a trained obstetrician and gynecologist, I know firsthand the impact of preterm birth on Black women and birthing people. I also know that racism – not race – is the driving factor leading the disproportionate impact of preterm birth on Black women and birthing people thereby exacerbating systemic inequities in maternal and infant health. To achieve birth equity, which is the assurance of the conditions of optimal births for all people with a willingness to address racial and social inequities in a sustained effort, we must work to protect and uphold a standard of care for spontaneous, recurrent preterm births and ensure it remains accessible and affordable for all who stand in need,” added Dr. Joia Crear Perry, founder and president of the National Birth Equity Collaborative.

The Preterm Birth Prevention Alliance is calling for the FDA to grant a public hearing to fully consider all of the data, additional research methods, and stakeholder perspectives before deciding whether to withdraw approval of this critical class of therapies. The health of America’s moms and babies warrants the utmost care and consideration.

###

ABOUT THE PRETERM BIRTH PREVENTION ALLIANCE

The Preterm Birth Prevention Alliance is a coalition of maternal and women’s health advocates who share a common concern about the state of preterm birth in the United States and the proposed market withdrawal of 17P, the only FDA-approved class of treatments to help prevent spontaneous, recurrent preterm birth. Formed in 2021 by the National Consumers League, we seek to improve preterm birth outcomes in the United States by maintaining access to safe, FDA-approved treatment options and advocating for more diverse medical research that adequately represents the experiences of women and newborns of color. Women of color need a seat at the table. To learn more, visit www.pretermbirthalliance.org.

Initial support for the Preterm Birth Prevention Alliance is provided by Covis Pharma.

MEDIA CONTACT:

Carol McKay, carolm@nclnet.org

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