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Press Releases

Featured Content

“Congress just put America last”— NCL slams Senate for undermining clean air, consumer rights

May 22, 2025
May 22, 2025: Washington, DC – Today, the United States Senate passed three Congressional Review Act (CRA) resolutions that restrict states’ rights to establish robust tailpipe emission standards.  Having passed the House of Representatives, these resolutions will now go to the President’s desk for signature.  
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https://nclnet.org/wp-content/uploads/2025/02/Social-Media-Images-20.png 788 940 Lisa McDonald https://nclnet.org/wp-content/uploads/2020/08/NCL-logo.png Lisa McDonald2025-05-22 20:07:202025-05-22 20:07:20“Congress just put America last”— NCL slams Senate for undermining clean air, consumer rights

NCL urges FDA and consumers to take action as GLP-1 shortage ends, but “infodemic” continues

May 21, 2025
May 21, 2025: Washington, DC — Despite the end of the GLP-1 shortage and May 22 FDA-issued deadline for companies to stop mass compounding of the products, the National Consumers League (NCL) is concerned that the epidemic of GLP-1 misinformation will continue to confuse consumers with fake products that can put their health at risk. Both the U.S. Food and Drug Administration (FDA) and consumers have roles to play in responding to the “infodemic.”
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https://nclnet.org/wp-content/uploads/2025/04/The-Weight-Truth-Banner-17.png 1036 2048 Lisa McDonald https://nclnet.org/wp-content/uploads/2020/08/NCL-logo.png Lisa McDonald2025-05-21 04:30:592025-05-21 15:19:34NCL urges FDA and consumers to take action as GLP-1 shortage ends, but “infodemic” continues

DOT’s abandonment of Southwest litigation will leave passengers worse off 

May 19, 2025
May 19, 2025: Washington, DC -- Last week, the U.S. Department of Transportation (DOT) quietly dropped its historic lawsuit against Southwest Airlines, which had originally been filed over the carrier’s unrealistic scheduling. The litigation would have been the first time an airline attempted to defend its chronic delays in court.   
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PreviousNext

CFPB layoffs significantly raise consumers’ risk of fraud 

April 17, 2025
April 17, 2025: Washington, DC – The National Consumers League (NCL) is calling on the Trump Administration to immediately stop the sweeping layoffs announced at the Consumer Financial Protection Bureau (CFPB). Reports that the Administration plans to lay off 1,500 positions across the CFPB's enforcement and supervision divisions will drastically reduce the agency's ability to fulfill its core mission of protecting consumers.    
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https://nclnet.org/wp-content/uploads/2025/04/Social-Media-Images-13.png 788 940 Lisa McDonald https://nclnet.org/wp-content/uploads/2020/08/NCL-logo.png Lisa McDonald2025-04-17 20:40:092025-05-07 23:43:41CFPB layoffs significantly raise consumers’ risk of fraud 

NCL warns: DOGE’s FTC infiltration puts consumer privacy at risk

April 14, 2025
April 14, 2025: Washington, DC – The National Consumers League (NCL) is outraged by the recent actions of Elon Musk's "Department of Government Efficiency" (DOGE), which has reportedly infiltrated the Federal Trade Commission (FTC). These actions pose a direct and immediate threat to consumers and parents nationwide. By interfering with the FTC's ability to protect the public—especially children's data—from harmful privacy violations, fraud, and anti-competitive practices, DOGE has crossed the line.  
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https://nclnet.org/wp-content/uploads/2025/04/Social-Media-Images-12.png 788 940 Lisa McDonald https://nclnet.org/wp-content/uploads/2020/08/NCL-logo.png Lisa McDonald2025-04-14 16:10:052025-05-07 23:45:08NCL warns: DOGE’s FTC infiltration puts consumer privacy at risk

New anti-child labor campaign targets major U.S. meat companies for illegal child labor in slaughterhouses

April 10, 2025
April 10, 2025: Washington, DC – Green America and the Child Labor Coalition launched a new campaign aimed at eradicating child labor and labor violations in the food production industry, with a focus on the four top U.S. meat processing companies. The campaign will focus on child labor and labor violations at Perdue Farms, JBS, Tyson and Cargill, including launching a consumer petition and engaging a network of allied grassroots groups on the ground across the country. 
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https://nclnet.org/wp-content/uploads/2025/04/iStock-1282616175-meat2-scaled.jpg 1708 2560 Lisa McDonald https://nclnet.org/wp-content/uploads/2020/08/NCL-logo.png Lisa McDonald2025-04-10 16:57:252025-05-07 23:46:46New anti-child labor campaign targets major U.S. meat companies for illegal child labor in slaughterhouses

U.S. House vote exposes more families to fraud  

April 9, 2025
April 9, 2025: Washington, DC – The National Consumers League (NCL) is outraged by today's partisan vote by the U.S. House of Representatives to repeal the Consumer Financial Protection Bureau's (CFPB) Larger Participants Rule. The vote approving S.J. Res 28 solidifies a gaping regulatory loophole that will allow Big Tech payment apps like PayPal, Venmo, and CashApp to evade accountability for their use by criminals to defraud millions of Americans.  
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Consumers deserve slave-free chocolate: new scorecard holds brands accountable     

April 8, 2025
April 8, 2025: Washington, DC – The National Consumers League (NCL) and its organization, the Child Labor Coalition (CLC), are proud to participate in the launch of the Annual Chocolate Scorecard, an initiative coordinated by Be Slavery Free, an Australian coalition campaigning against modern slavery. This campaign aims to raise awareness about child labor in chocolate production, promote ethical sourcing, and empower consumers to choose chocolate that aligns with their values.     
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https://nclnet.org/wp-content/uploads/2025/04/Chocolatescorecard_logo_Brown_Vertical.png 1947 1579 Lisa McDonald https://nclnet.org/wp-content/uploads/2020/08/NCL-logo.png Lisa McDonald2025-04-08 20:08:472025-05-07 23:47:22Consumers deserve slave-free chocolate: new scorecard holds brands accountable     

NCL hails bipartisan committee vote on TICKET act

April 8, 2025
April 8, 2025: Washington, DC - The National Consumers League today applauded the House Energy and Commerce committee for its overwhelming and bipartisan vote to approve the TICKET Act (H.R. 1402). The TICKET Act would, for the first time in history, ensure accountability and fairness in live event ticketing across the United States. The bill, which passed the U.S. House last Congress 388-24, was recently reported unanimously out of the Senate Commerce Committee. The bill has previously received support from nearly every stakeholder in the live event ecosystem, including consumer organizations, free-market advocates, venues, artists, primary and secondary ticketing platforms, and more than 37,000 individual fans.
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https://nclnet.org/wp-content/uploads/2025/04/Social-Media-Images-3.png 788 940 Lisa McDonald https://nclnet.org/wp-content/uploads/2020/08/NCL-logo.png Lisa McDonald2025-04-08 18:45:052025-05-07 23:47:32NCL hails bipartisan committee vote on TICKET act

NCL slams introduction of resolutions weakening tailpipe emission standards

April 4, 2025
April 4, 2025, Washington, DC – Congressional Republicans today introduced three Congressional Review Act (CRA) resolutions that restricts states’ rights to establish robust tailpipe emission standards. 
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https://nclnet.org/wp-content/uploads/2025/04/Social-Media-Images-10.png 788 940 Lisa McDonald https://nclnet.org/wp-content/uploads/2020/08/NCL-logo.png Lisa McDonald2025-04-04 13:59:242025-04-04 14:03:50NCL slams introduction of resolutions weakening tailpipe emission standards

NCL welcomes President Trump’s Executive Order and calls for congressional action on consumer protections in live-event ticketing

March 31, 2025
March 31, 2025: Washington, DC – The National Consumers League (NCL) is commending President Donald J. Trump for signing an Executive Order aimed at protecting fans from exploitative ticket scalping and implementing common sense reforms in the live entertainment ticketing industry. This decisive action underscores the urgent need for Congress to pass the bipartisan Transparency in Charges for Key Events Ticketing (TICKET) Act (S.281/H.R. 1402).
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Big banks win, consumers lose: NCL condemns effort to kill CFPB overdraft rule   

March 28, 2025
March 28, 2025: Washington, DC – The National Consumers League (NCL) strongly opposes efforts to rescind the Consumer Financial Protection Bureau's (CFPB) new overdraft fee rule through the Congressional Review Act (CRA). This rule is a critical step in closing an outdated loophole that has allowed major banks to rake in billions from excessive overdraft fees—often at the expense of hardworking families living paycheck to paycheck.   
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Mass layoffs at HHS: A blow to healthcare access and public health

March 27, 2025
March 27, 2025: Washington, DC – The National Consumers League (NCL) is deeply concerned by the Trump administration's decision to lay off an additional 10,000 employees at the Department of Health and Human Services (HHS) following the already eliminated 10,000 jobs via previous rounds of cuts. In total, the restructuring and force reduction plans will result in a downsizing from 82,000 to 62,000 full-time employees nationwide.
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Subject Matter Experts

Consumer issues (general), workers’ rights issues: Sally Greenberg

Privacy, telecommunications, fraud, travel and entertainment industries, data security: John Breyault

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Health care policy: Sally Greenberg

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Consumer literacy and teens’ spending habits, education: Lisa Hertzberg

Sally Greenberg

Sally Greenberg joined the National Consumers League as Executive Director on October 1, 2007. The League’s focus is on five key priority areas: fraud, child labor, LifeSmarts, health care, especially the safe use of medications and medication adherence, and food safety and nutrition.

Latest Press Releases

NCL urges FDA and consumers to take action as GLP-1 shortage ends, but “infodemic” continues

May 21, 2025/in Featured Home - Food & Nutrition, Featured Home - Your Health, Press release Press Releases, Statements /by Lisa McDonald

May 21, 2025: Washington, DC — Despite the end of the GLP-1 shortage and May 22 FDA-issued deadline for companies to stop mass compounding of the products, the National Consumers League (NCL) is concerned that the epidemic of GLP-1 misinformation will continue to confuse consumers with fake products that can put their health at risk. Both the U.S. Food and Drug Administration (FDA) and consumers have roles to play in responding to the “infodemic.”

Read more
https://nclnet.org/wp-content/uploads/2025/04/The-Weight-Truth-Banner-17.png 1036 2048 Lisa McDonald https://nclnet.org/wp-content/uploads/2020/08/NCL-logo.png Lisa McDonald2025-05-21 04:30:592025-05-21 15:19:34NCL urges FDA and consumers to take action as GLP-1 shortage ends, but “infodemic” continues

DOT’s abandonment of Southwest litigation will leave passengers worse off 

May 19, 2025/in Featured Home - Consumer Protection, Press release Press Releases, Statements /by Lisa McDonald

May 19, 2025: Washington, DC — Last week, the U.S. Department of Transportation (DOT) quietly dropped its historic lawsuit against Southwest Airlines, which had originally been filed over the carrier’s unrealistic scheduling. The litigation would have been the first time an airline attempted to defend its chronic delays in court.   

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NCL Denounces Illegal Attempt to Fire CPSC Commissioners

May 9, 2025/in Featured Home - Consumer Protection, Press release Press Releases, Statements /by allisonc

May 9, 2025: Washington, DC – Washington, DC – The National Consumers League calls on the Trump administration to rescind the illegal attempt to fire Democratic Commissioners on the Consumer Product Safety Commission (CPSC). “This unprecedented assault on our nation’s regulator of household product safety is in direct contravention of the spirit and letter of the law, runs afoul of decades of Supreme Court precedent, and threatens to cripple the CPSC’s ability to carry out its lifesaving mission,” said Daniel Greene, the Senior Director of Consumer Protection & Product Safety at the National Consumers League.

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158 Advocates Send Letter Opposing Plan to Eliminate the CPSC

May 8, 2025/in Featured Home - Consumer Protection, Press release Press Releases, Statements /by Lisa McDonald

May 8, 2025: Washington, DC – Today, the National Consumers League, Consumer Federation of America, Consumer Reports, and 156 other product safety advocates sent a letter to Russell Vought, the Director of the Office of Management and Budget, expressing their strong opposition to any attempt to eliminate, defund, or weaken the Consumer Product Safety Commission (CPSC).

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National Survey Shows a Vast Majority of Americans Want Comprehensive Reform of the 340B Drug Pricing Program

May 8, 2025/in Featured Home - Your Health, Press release Press Releases /by allisonc

May 8, 2025: Washington, DC – Today, the National Consumers League (NCL) released results from a new Morning Consult national poll of more than 10,000 American adults, revealing overwhelming concern about the burden of medical debt and strong public demand for comprehensive reforms of the 340B Drug Pricing Program. Nearly four in five surveyed adults (78%) support establishing requirements to ensure that qualifying patients directly benefit from 340B drug discounts through reduced out-of-pocket prescription drug costs. More than three in four surveyed adults (77%) believe hospitals should be required to pass 340B savings directly onto patients.

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https://nclnet.org/wp-content/uploads/2025/05/Social-Media-Images-70.png 788 940 allisonc https://nclnet.org/wp-content/uploads/2020/08/NCL-logo.png allisonc2025-05-08 13:36:592025-05-08 13:46:14National Survey Shows a Vast Majority of Americans Want Comprehensive Reform of the 340B Drug Pricing Program
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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.

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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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