Jill Biden lands new job following four years as first lady
Jill Biden landed a new job following her four years in the White House: leading a California-based think tank's initiative aimed at improving women's health.
'From endometriosis to healthy aging, the White House Initiative on Women's Health Research made important investments in research and development, while making clear it will take collaboration across industries to bring these innovations to scale,' Biden said, according to a Milken Institute press release published April 29. 'I am honored to join the Milken Institute as we unite leaders around a shared mission: for women everywhere to benefit from the lifesaving, world-changing research we know is possible.'
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The Milken Institute describes itself as a nonpartisan economic think tank based out of Santa Monica that focuses on 'financial, physical, mental, and environmental health' to 'bring together the best ideas and resourcing to develop blueprints for tackling some of our most critical global issues.' Biden will serve as the chair of the think tank's new Women's Health Network.
Biden, who is a teacher and holds a doctorate in education, focused as first lady on the Biden Cancer Moonshot plan to end cancer, the Joining Forces initiative to support veteran families and caregivers, and launching the White House Initiative on Women's Health Research.
4 Jill Biden is set to lead a California-based think tank's initiative aimed at improving women's health following her time in the White House.
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Biden joined the Milken Institute's 28th annual Global Conference in Beverly Hills, California, Monday. Other notable guests who addressed the conference included Trump administration Treasury Secretary Scott Bessent, former British Prime Minister Tony Blair and Trump administration Centers for Medicare & Medicaid Services Administrator Mehmet Oz, the Los Angeles Daily News reported.
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Biden's new role serving as chair of the Milken Institute's initiative will focus on 'galvanizing participation, collaboration, and shared action in the Women's Health Network to improve women's health and wellbeing,' according to the think tank's press release announcing the former first lady's new role.
Former President Joe Biden signed a presidential memorandum in 2023 that launched the White House Initiative on Women's Health Research. Jill Biden led the White House initiative, which worked to beef up funding for and research into women's health.
4 According to a press release, Biden's new role will focus on 'galvanizing participation, collaboration, and shared action in the Women's Health Network to improve women's health and wellbeing.'
JHVEPhoto – stock.adobe.com
The Biden White House argued at the time that 'TOO MANY medical studies have focused on men and left women out' and that too many of 'the medicine dosages, treatments, medical school text books, are based on men and their bodies – and that information doesn't always apply to women.'
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Jill Biden said during Milken's conference Monday that her husband had been eager to 'infuse' the 'federal government with money' when they launched the White House women's health initiative in 2023.
'So one of the things we did was we got to work right away,' Jill Biden said during the Milken Institute conference Monday. 'Joe said, 'You know, let's infuse – really, the federal government with money.' In one year, we put in $1 billion to advance women's research.'
4 President Joe Biden and first lady Jill Biden listen as Maria Shrive speaks during a Women's History Month reception, an event part of the Biden administration's Women's Health Research initiative.
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'And we worked a lot through the (National Institutes of Health) and the way that they did research, and we made sure that they disaggregated the data and that they separated the research on women and men differently, and we worked with (the Department of Defense) DOD – they put a lot of money into women's research – and then we put a lot of money in to de-risk the investment. So there were a lot of things that, really, private equity wasn't willing to take on because it was too risky, and we thought, let's push this forward, and let's try to find answers more quickly.'
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Fox News Digital reached out to the Milken Institute Tuesday for additional comment on the former first lady's new role, but did not immediately receive a reply.
Jill Biden worked as a professor at Northern Virginia Community College from 2009 to December 2024, when she announced she wrapped up her final semester as her husband prepared for his Oval Office exit.
4 'We made sure that they disaggregated the data and that they separated the research on women and men differently,' the former first lady said.
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Jill Biden's new role comes as political books recapping the Biden administration hit bookshelves nationwide, with several reporting that concerns over the president's mental acuity and age had gripped the administration across its four years.
The book '2024: How Trump Retook the White House and the Democrats Lost America,' for example, is set to be released in July and authored by three reporters from the Wall Street Journal, The New York Times and Washington Post, and reportedly details how Biden's team chose not to have the president take a cognitive test in February 2024 due to concerns that taking the test itself would raise more questions about his age.
Another book, Chris Whipple's 'Uncharted: How Trump Beat Biden, Harris, and the Odds in the Wildest Campaign in History,' reported that White House staffers allegedly kept Biden from socializing with others, including close allies and friends, out of fear the 46th president 'might say the wrong thing or might feed the mental acuity narrative.'
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With up to three years of follow-up, a single dose of lonvo-z led to a 98% mean reduction in monthly HAE attack rate in all 10 patients All 10 patients were attack-free and treatment-free for a median of 23 months through the latest follow-up, demonstrating the potential of lonvo-z to become the first one-time therapy for most HAE patients Lonvo-z was well tolerated and continues to demonstrate a favorable safety profile The global Phase 3 HAELO trial of lonvo-z has concluded screening ahead of schedule with more than half screened from U.S. sites; Intellia to provide an update on enrollment in the future CAMBRIDGE, Mass., June 15, 2025 (GLOBE NEWSWIRE) — Intellia Therapeutics, Inc. 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At the time of the February 12 data cutoff, patients were attack-free and treatment-free for a median of nearly two years. With up to three years of follow-up, a single dose of lonvo-z led to a mean reduction in monthly HAE attack rate of 98% over the study period, compared to pre-treatment baseline. For all 10 patients, deep, dose-dependent and durable reductions in plasma kallikrein protein continued to be observed through the latest assessment. Safety Across all three dose levels, lonvo-z has been well tolerated and continues to demonstrate a favorable safety profile consistent with earlier data presented at EAACI in 2024. The most frequent adverse events during the study period were infusion-related reactions (IRRs). IRRs were mostly Grade 1 and resolved with all patients receiving the full dose. With up to 3 years of follow-up, no treatment-emergent serious adverse events were observed, and no treatment-related adverse events were observed during the period following 28 days after dosing. Clinical Development Plans Intellia's global Phase 3, randomized, double-blind, placebo-controlled HAELO trial is ongoing to assess the safety and efficacy of lonvo-z at the 50 mg dosage. The Company announced today the HAELO trial has successfully completed screening ahead of schedule, with over half of the patients being screened in the United States. The study is no longer recruiting and Intellia will provide an update on enrollment in the future. New and longer-term data from the Phase 2 portion of the ongoing Phase 1/2 study is planned to be presented in the second half of 2025. Intellia expects to submit a biologics license application (BLA) in 2026 to support the Company's plans for a U.S. launch in 2027. For more information on HAELO (NCT06634420), please visit About the Lonvoguran Ziclumeran (lonvo-z, also known as NTLA-2002) Clinical Program Intellia's ongoing Phase 1/2 study is evaluating the safety and efficacy of lonvo-z in adults with Type I or Type II hereditary angioedema (HAE). The Phase 1 portion of the study is an international, open-label study designed to identify the dose level of lonvo-z selected for further evaluation in the Phase 2 portion of the study. Enrollment in both portions of the Phase 1/2 study is complete. Intellia dosed the first patient in the global Phase 3, randomized, double-blind, placebo-controlled HAELO trial in January of 2025. Visit (NCT05120830) for more details. About Lonvo-z Based on Nobel Prize-winning CRISPR/Cas9 technology, lonvo-z has the potential to become the first one-time treatment for hereditary angioedema (HAE). Lonvo-z is an investigational in vivo CRISPR-based gene editing therapy designed to prevent HAE attacks by inactivating the kallikrein B1 ( KLKB1 ) gene, which encodes for prekallikrein, the kallikrein precursor protein. Interim Phase 1/2 clinical data showed dramatic reductions in attack rate, as well as consistent, deep and durable reductions in kallikrein levels. Lonvo-z has received five notable regulatory designations, including Orphan Drug and RMAT Designation by the U.S. Food and Drug Administration (FDA), the Innovation Passport by the U.K. Medicines and Healthcare products Regulatory Agency (MHRA), Priority Medicines (PRIME) Designation by the European Medicines Agency, as well as Orphan Drug Designation (ODD) by the European Commission. About Intellia Therapeutics Intellia Therapeutics, Inc. (NASDAQ:NTLA) is a leading clinical-stage gene editing company focused on revolutionizing medicine with CRISPR-based therapies. Since its inception, Intellia has focused on leveraging gene editing technology to develop novel, first-in-class medicines that address important unmet medical needs and advance the treatment paradigm for patients. Intellia's deep scientific, technical and clinical development experience, along with its people, is helping set the standard for a new class of medicine. To harness the full potential of gene editing, Intellia continues to expand the capabilities of its CRISPR-based platform with novel editing and delivery technologies. Learn more at and follow us @intelliatx. Forward-Looking Statements This press release contains 'forward-looking statements' of Intellia Therapeutics, Inc. ('Intellia' or the 'Company') within the meaning of the Private Securities Litigation Reform Act of 1995. These forward-looking statements include, but are not limited to, express or implied statements regarding Intellia's beliefs and expectations concerning: the safety, efficacy, success and advancement of its clinical programs for lonvoguran ziclumeran or 'lonvo-z' (also known as NTLA-2002) for hereditary angioedema ('HAE'), including the ability to successfully complete its global Phase 3 HAELO study; its expectation to present additional data regarding lonvo-z, including reporting outcomes of the Phase 3 HAELO study in the first half of 2026 and presenting new and longer-term data from the Phase 2 portion of the ongoing Phase 1/2 study of lonvo-z in the second half of 2025; and its expectation to be able to support a biologics license application for lonvo-z for the treatment of HAE by 2026 for a U.S. launch in 2027. Any forward-looking statements in this press release are based on management's current expectations and beliefs of future events and are subject to a number of risks and uncertainties that could cause actual results to differ materially and adversely from those set forth in or implied by such forward-looking statements. These risks and uncertainties include, but are not limited to: risks related to Intellia's ability to protect and maintain its intellectual property position; risks related to Intellia's relationship with third parties, including its contract manufacturers, licensors and licensees; risks related to the ability of its licensors to protect and maintain their intellectual property position; risks related to Intellia's ability to protect and maintain its intellectual property position; risks related to valid third party intellectual property; risks related to Intellia's relationship with third parties, including its licensors and licensees; risks related to the ability of its licensors to protect and maintain their intellectual property position; uncertainties related to regulatory agencies' evaluation of regulatory filings and other information related to our product candidates, including lonvo-z; uncertainties related to the authorization, initiation and conduct of studies and other development requirements for our product candidates, including uncertainties related to regulatory approvals to conduct clinical trials, including our ability to complete the Phase 3 HAELO study for HAE; the risk that any one or more of Intellia's product candidates, including lonvo-z, will not be successfully developed and commercialized; and the risk that the results of preclinical studies or clinical studies will not be predictive of future results in connection with future studies for the same product candidate or Intellia's other product candidates. For a discussion of these and other risks and uncertainties, and other important factors, any of which could cause Intellia's actual results to differ from those contained in the forward-looking statements, see the section entitled 'Risk Factors' in Intellia's most recent annual report of Form 10-K and quarterly report on Form 10-Q, as well as discussions of potential risks, uncertainties, and other important factors in Intellia's other filings with the Securities and Exchange Commission. All information in this press release is as of the date of the release, and Intellia undertakes no duty to update this information unless required by law. Intellia Contacts: Investors:Brittany ChavesSenior Manager, Investor Relations [email protected]
