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X-WR-CALNAME:Hemophilia Alliance
X-ORIGINAL-URL:https://hemoalliance.org
X-WR-CALDESC:Events for Hemophilia Alliance
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DTSTART;TZID=America/New_York:20241211T130000
DTEND;TZID=America/New_York:20241211T140000
DTSTAMP:20260403T172506
CREATED:20241126T181513Z
LAST-MODIFIED:20241126T182239Z
UID:69641-1733922000-1733925600@hemoalliance.org
SUMMARY:🟥 Member Webinar : Hemophilia Alliance Hosts - A webinar from CSL Behring - Learn about HEMGENIX from the patient perspective
DESCRIPTION:Date: Wednesday\, December 11\, 2024\nTime: 1:00pm – 2:00pm ET \n \n  \n  \n  \n  \n \nTOPIC: \nLearn about HEMGENIX from the patient perspective \nOBJECTIVE: \nMichael will share his personal experience after receiving HEMGENIX \nRECOMMENDED AUDIENCE: \nHTC providers\, social workers\, administration and support staff \nSPEAKER: \nMichael – Common Factors Advocate Hemophilia B \n \nMy Life at a Glance – At the age of four\, I was diagnosed with hemophilia B factor IX deficiency. My parents told me that this disorder would limit me and that I would most likely have to progress through life with caution. So\, at a very young age\, I was forced to make an adult decision. I had to either learn how to manage \n my hemophilia or accept the possible limitations that were awaiting a severe hemophiliac. When I was a kid\, I made sure to not let hemophilia get in the way by staying on top of managing it. It was hard to accept help from anyone because I wanted to do it on my own. It was my superpower\, not theirs. \nMy previous local support group was amazing. They organized scholarships and had activities that were safe for hemophilia patients. It was a close-knit community. I even volunteered there! After finding the right treatment for me\, I have noticed myself living a more stress-free lifestyle; I no longer have to infuse a minimum of twice a month to maintain my factor levels. \nMy Message to the Community – Hemophilia is our superpower. It’s time to don that cape and advocate for yourself.
URL:https://hemoalliance.org/alliance-events/a-webinar-from-csl-behring-learn-about-hemgenix-from-the-patient-perspective/
CATEGORIES:Members Only
ATTACH;FMTTYPE=image/jpeg:https://hemoalliance.org/wp-content/uploads/2023/12/CSL-Behring.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20241217T150000
DTEND;TZID=America/New_York:20241217T160000
DTSTAMP:20260403T172506
CREATED:20241126T182846Z
LAST-MODIFIED:20241126T182846Z
UID:69645-1734447600-1734451200@hemoalliance.org
SUMMARY:🟥 Member Webinar : Hemophilia Alliance Hosts - A webinar from Pfizer on HYMPAVZI: An anti-tissue factor pathway inhibitor
DESCRIPTION:Date: Tuesday\, December 17\, 2024\nTime: 3:00pm – 4:00pm ET \n \n  \n  \n  \n  \n \nTOPIC: \nHYMPAVZI: An anti-tissue factor pathway inhibitor \nOBJECTIVE: \nTo educate attendees on the novel mechanism of action of HYMPAVZI\, the Ph3 clinical trial results and indicated dosage and administration. \nINTENDED AUDIENCE: \nHCP \nSPEAKER: \nDr. Jennifer Schumacher\, PhD\, Senior Medical Director\, Hemophilia \n \nJennifer Schumacher Sr. Medical Director has over 21 years of Medical Affairs and Biotech Industry experience. Currently\, a senior medical director in hemophilia\, Jennifer is the US medical lead for marstacimab. During her tenure at Pfizer\, she has held several positions beginning in US Medical Affairs in Oncology and transitioning to medical director in Rare Disease where she has lead the global medical team for transthyretin amyloid (ATTR) cardiomyopathy and served as publications lead. Jennifer joined the US hemophilia medical team in 2023. \nJennifer received her PhD in Pharmacology from the University of Minnesota\, Minneapolis\, USA and a B.S. in Biotechnology and Chemistry from St. Cloud State University\, St. Cloud\, USA. \nJennifer is based in Minneapolis\, Minnesota and enjoys spending time with her husband and two children. She loves reading\, cooking and the great outdoors\, snowmobiling in the winter and spending time with family and friends at their cabin in the summer.
URL:https://hemoalliance.org/alliance-events/a-webinar-from-pfizer-on-hympavzi-an-anti-tissue-factor-pathway-inhibitor/
CATEGORIES:Members Only
ATTACH;FMTTYPE=image/jpeg:https://hemoalliance.org/wp-content/uploads/2024/01/Pfizer.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20241218T130000
DTEND;TZID=America/New_York:20241218T140000
DTSTAMP:20260403T172506
CREATED:20241101T163407Z
LAST-MODIFIED:20241101T163925Z
UID:69340-1734526800-1734530400@hemoalliance.org
SUMMARY:🟥 Member Webinar : Hemophilia Alliance Hosts - A Webinar from Novo Nordisk - Unmet Needs in Current Hemophilia Care: From Burdens to Breakthroughs
DESCRIPTION:Date: Wednesday\, December 18\, 2024\nTime: 1:00pm – 2:00pm ET \n \n  \n  \n  \n  \n \nTitle: \nUnmet Needs in Current Hemophilia Care: From Burdens to Breakthroughs \nDescription and Session Objectives: \nTo provide a clinical overview of the cost and treatment burden across all hemophilia types\, the experience with current therapy\, and unmet needs that may be addressed with novel therapies. \nTarget Audience: \nAll HTC Staff \nSpeakers: \nParin Chikani PharmD\, MBA \nRyan Rodriguez PharmD\, MS\, BCPS \n \nParin Chikani\, lives in the Chicagoland area and earned his Doctorate of Pharmacy degree from the University of Illinois at Chicago\, College of Pharmacy and his MBA from Kellstadt Graduate School of Business. Before joining Novo Nordisk\, Parin had been in the Pharmacy/Managed Care setting for over 15 years where he held many different roles and leadership positions within Pharmacy and Medical areas of the business. At Novo Nordisk\, one of his roles and responsibilities is to ensure payors and clinicians are up-to-date on evidence based clinical and scientific information in the areas of Rare Diseases to help assist them with patient care. \n \nRyan Rodriguez is a Medical Liaison for rare blood disorders at Novo Nordisk covering the Midwest. His responsibilities include learning from and sharing medical information with clinicians who treat patients with hemophilia and other bleeding disorders\, aligning with his passion for evidence-based patient care. Prior to joining Novo Nordisk\, Ryan earned his PharmD degree from the University of Florida\, and then served as Clinical Associate Professor at the University of Illinois Chicago College of Pharmacy\, where he also earned his Master’s degree in epidemiology. Throughout his career\, Ryan has been involved in medical communications\, evidence generation and publication\, and formulary management for various public and private entities.
URL:https://hemoalliance.org/alliance-events/a-webinar-from-novo-nordisk-unmet-needs-in-current-hemophilia-care-from-burdens-to-breakthroughs/
CATEGORIES:Members Only,Webinar
ATTACH;FMTTYPE=image/png:https://hemoalliance.org/wp-content/uploads/2023/09/Standard-Manufacturing-Partners-Novo_width_191px.png
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20250122
DTEND;VALUE=DATE:20250125
DTSTAMP:20260403T172506
CREATED:20240618T181011Z
LAST-MODIFIED:20241105T171358Z
UID:65968-1737504000-1737763199@hemoalliance.org
SUMMARY:🟥 Member Event : 2025 Pharmacists CE Conference
DESCRIPTION:Date: January 22 – 24\, 2025\nLocation: The Westin San Diego Gaslamp Quarter\, San Diego\, CA 92101 \n \nHemophilia Alliance is proud to announce the 4th Annual Pharmacists CE Conference. The conference is designed specifically for Hemophilia Alliance Member HTC pharmacists with direct responsibility for 340B HTC dispensations. \nThere will be 40 spaces available for the in-person conference. Attendees will be randomly chosen from the pool of applicants. For those who cannot attend in person\, a virtual option will be available. \nApplicants will be notified by November 22nd of their invitation to attend the conference. If you are invited to attend the conference\, please verify that you will be able to attend the conference in its entirety before accepting. We will begin working on flight arrangements as soon as November 25th\, 2024. \nAttendees will require a commitment of arrival on Wednesday\, January 22nd by 6:30pm\, with the meeting ending at 3:30 pm on Friday\, January 24th. Hemophilia Alliance will underwrite each participant’s air travel\, transfers to and from the hotel\, hotel accommodations and group meals. \nThe application period is now open through November 15th\, 2024 \n\n \nPlease contact Mark Plencner with any questions regarding this registration at mark@hemoalliance.org or 701-318-2910.
URL:https://hemoalliance.org/alliance-events/2025-pharmacist-ce-conference/
CATEGORIES:Members Only
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20250219T130000
DTEND;TZID=America/New_York:20250219T140000
DTSTAMP:20260403T172506
CREATED:20250204T192346Z
LAST-MODIFIED:20250204T192346Z
UID:70040-1739970000-1739973600@hemoalliance.org
SUMMARY:🟥 Member Webinar : Hemophilia Alliance Hosts - A webinar from BioMarin on ROCTAVIAN: Improving Patient Outcomes - Latest Data & Support Initiatives
DESCRIPTION:Date: Wednesday\, February 19\, 2025\nTime: 1:00pm – 2:00pm ET \n  \n \n  \n  \n \nTITLE: \nROCTAVIAN: Improving Patient Outcomes – Latest Data & Support Initiatives \nOBJECTIVE: \nJoin us for a webinar on ROCTAVIAN (valoctocogene roxaparvovec)\, the groundbreaking gene therapy for severe hemophilia A. This webinar will delve into the latest clinical data updates\, showcasing the long-term efficacy and safety of ROCTAVIAN. We’ll also hear a firsthand experience from one of the patients who has received ROCTAVIAN\, offering valuable insights into the real-world impact of this therapy. Finally\, we will explore the comprehensive support programs available to patients\, ensuring access to information\, resources\, and assistance throughout the treatment journey. \nINTENDED AUDIENCE: \nProviders\, HTC staff\, business administrators and decision makers \nSPEAKERS: \n\nPatrick Fogarty\, Executive Medical Director\, US Medical Lead\, Hemophilia\, GMAF\nNick Campbell\, Senior Director\, Patient Support Programs
URL:https://hemoalliance.org/alliance-events/a-webinar-from-biomarin-on-roctavian-improving-patient-outcomes-latest-data-support-initiatives/
CATEGORIES:Members Only,Webinar
ATTACH;FMTTYPE=image/png:https://hemoalliance.org/wp-content/uploads/2022/02/Standard-Manufacturing-Partners-Biomarin_height_191px.png
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20250226T180000
DTEND;TZID=America/New_York:20250228T140000
DTSTAMP:20260403T172506
CREATED:20240618T181218Z
LAST-MODIFIED:20250205T135322Z
UID:65969-1740592800-1740751200@hemoalliance.org
SUMMARY:🟥 Member Event : 2025 Linda Gammage Social Workers CE Conference
DESCRIPTION:Date: February 26 – 28\, 2025\nLocation: Austin\, TX \n \nPlease contact Jeff Amond with any questions regarding this registration at amond@hemoalliance.org or 608-206-3132.
URL:https://hemoalliance.org/alliance-events/2025-linda-gammage-social-worker-ce-conference/
CATEGORIES:Members Only
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20250309T183000
DTEND;TZID=America/New_York:20250311T153000
DTSTAMP:20260403T172506
CREATED:20240816T142513Z
LAST-MODIFIED:20241211T224011Z
UID:68221-1741545000-1741707000@hemoalliance.org
SUMMARY:🟥 Member Event : 2025 Spring Members Meeting
DESCRIPTION:Date: March 9 – 11\, 2025\nLocation: Salt Lake City\, Utah \n \nPlease contact Theresa Parker with any questions regarding this registration at theresa@hemoalliance.org or 727-688-2568.
URL:https://hemoalliance.org/alliance-events/member-event-2025-spring-members-meeting/
CATEGORIES:Members Only
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20250319T120000
DTEND;TZID=America/New_York:20250319T130000
DTSTAMP:20260403T172506
CREATED:20250305T232342Z
LAST-MODIFIED:20250306T153859Z
UID:70280-1742385600-1742389200@hemoalliance.org
SUMMARY:🟥 Member Webinar : Hemophilia Alliance Presents - Updates from Washington: Administration and Congressional Actions
DESCRIPTION:Date: Wednesday\, March 19th\, 2025\nTime: 12:00pm – 1:00pm ET \n \nWEBINAR TOPIC: \nUpdates from Washington: Administration and Congressional Actions \nOBJECTIVE: \n\nThe current status of government funding for fiscal year 2025.\nThe potential impact of the new Administration’s early actions\, including Executive Orders\, reduction in agency staffing\, changes to the regulatory process and how this may impact federal agencies\, programs\, and policies important to HTCs.\nExpected Congressional actions on a Budget Reconciliation bill(s) to extend tax cuts and find savings in Medicaid and Medicare and the future of 340B Reforms.\n\nTARGET AUDIENCE: \nAll HTC staff or HTC Leadership\, Administration and Policy Teams \nSPEAKERS: \n\nDean Hindenlang\, PhD\, Hemophilia Alliance Vice Chair\nEllen Riker and Miriam Goldstein\, Hemophilia Alliance Federal Policy Advisors\, Artemis Policy Group\n\n  \n\n  \nDean M. Hindenlang has served the nonprofit and government sectors for almost 30 years\, focusing on strategic planning\, administrative oversight and governance\, and coalition-building through an equity-based lens. As Director of Public Policy and Strategic Initiatives with Cascade Hemophilia Consortium\, his work focuses on coalition-building while helping ensure that individuals needing assistance are advocated for in community and government-based capacities. He is a proven leader in assisting members of marginalized and underserved communities. \nMr. Hindenlang holds a Ph.D. in Public Policy and Administration\, completing his doctoral dissertation on equity in community-based programming. He has a Master of Public Administration\, a Master of Science in Marketing and Communication\, a Master of Healthcare Administration\, and a bachelor’s degree in English. Additionally\, he serves as an adjunct professor\, doctoral faculty methodologist\, and subject matter expert at Franklin University. He also offers undergraduate instruction on social justice and cultural awareness at Southern New Hampshire University. \nAs the Director of Public Policy and Strategic Initiatives\, Dean serves Cascade HC by engaging local and state authorities\, as well as elected officials\, on matters of public policy actions\, projects\, and patient education and advocacy. \n\n  \n \n Ellen Riker is a Principal with the Artemis Policy Group\, an association management and lobbying firm she established with Johanna Gray and Elizabeth Karan in April 2020 in Washington\, DC. Ellen advises several national patient organizations and medical societies on federal government affairs and health policy and has worked with the Hemophilia Alliance since 2010. As a federal policy advisor and lobbyist\, Ellen has managed federal strategies for corporate and non-profit organizations\, specializing in public and private insurance reimbursement and coverage policies\, biomedical and health services research\, and public health programs. \nEllen has worked with the many agencies of the Department of Health and Human Services and has been involved in the development of legislation coming out of the House and Senate committees with jurisdiction over Medicare\, Medicaid\, and public health service programs. Ellen served on the professional staff of the House Energy and Commerce Committee from 1983 – 1988\, with particular focus on health policy. Ellen received her master’s degree in health administration from Xavier University and a B.A. with honors from the University of Cincinnati. \n\n  \nMiriam Goldstein joined the Artemis Policy Group as a Senior Policy Advisor in August 2024 after more than seven years at Hemophilia Federation of America. Miriam focuses on federal and state policies impacting patient access to coverage\, access to care\, and affordability. Over the course of her legislative and regulatory work\, Miriam has developed expertise in the Affordable Care Act and insurance reform\, Medicaid eligibility and program requirements; and other keystones of the health policy landscape. \nBefore her time at HFA\, Miriam worked as an attorney in private practice and with the US Securities and Exchange Commission. Miriam earned her J.D. degree from the University of Pennsylvania and her B.A. in history from Yale. She is admitted to practice law in D.C. Miriam lives in Arlington\, Virginia\, and in her free time can often be found cycling on local bike trails with her husband Dave.
URL:https://hemoalliance.org/alliance-events/hemophilia-alliance-presents-update-from-washington-administration-and-congressional-actions/
CATEGORIES:Members Only,Webinar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20250320T140000
DTEND;TZID=America/New_York:20250320T150000
DTSTAMP:20260403T172506
CREATED:20250305T194737Z
LAST-MODIFIED:20250306T154410Z
UID:70275-1742479200-1742482800@hemoalliance.org
SUMMARY:🟥 Member Webinar : Hemophilia Alliance Hosts - A webinar from Takeda on FVIII Portfolio
DESCRIPTION:Date: Thursday\, March 20th\, 2025\nTime: 2:00pm – 3:00pm ET \n \n  \n  \n  \n \nTITLE: \nTakeda FVIII Portfolio \nOBJECTIVE: \nPlease join Takeda leadership to review Takeda FVIII Products & Resources Available. \nINTENDED AUDIENCE: \nAll HTC staff \nSPEAKER: \nAnthea Cherednichenko\, VP US Hematology Franchise Head \nAnthea leads the sales and marketing teams for Takeda’s Hematology portfolio. Anthea previously served as the General Manager for Takeda Austria. Prior to that role\, she was in Global and European leadership roles in Hematology based out of Switzerland. Originally from Australia\, Anthea spent her early career years in medical device and health IT marketing roles in both Australia and Asia\, before joining Baxter (later acquired by Takeda) in 2013. Anthea holds a Master of Public Health from the University of Sidney and Master of Business Administration from Victoria University.
URL:https://hemoalliance.org/alliance-events/a-webinar-from-takeda-on-fviii-portfolio/
CATEGORIES:Members Only,Webinar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20250403T140000
DTEND;TZID=America/New_York:20250403T150000
DTSTAMP:20260403T172506
CREATED:20250306T155911Z
LAST-MODIFIED:20250306T155911Z
UID:70300-1743688800-1743692400@hemoalliance.org
SUMMARY:🟥 Member Webinar : Hemophilia Alliance Hosts - A webinar from Novo Nordisk on Alhemo (concizumab-mtci): A new option for patients living with hemophilia A or B with inhibitors
DESCRIPTION:Date: Thursday\, April 3rd\, 2025\nTime: 2:00pm – 3:00pm ET \n \n  \n  \n  \n  \n \nWEBINAR TOPIC: \nAlhemo (concizumab-mtci): A new option for patients living with hemophilia A or B with inhibitors \nOBJECTIVE: \nTo provide a prescribing information overview of the recently FDA approved medication\, Alhemo (concizumab-mtci)\, for patients living with hemophilia A or B with inhibitors. \nINTENDED AUDIENCE: \nAll HTC staff \nSPEAKER: \nCraig Schmidt\, PharmD\, Medical Accounts Associate Director – Novo Nordisk Medical Affairs\n \nBefore joining Novo Nordisk\, Craig had been in the Community Pharmacy and Managed Care settings for 13 years and held various roles and leadership positions. Of note\, Craig was the Pharmacy Director of a Regional Health Plan that served over a million Medicaid\, Medicare\, and Commercially insured patients within the New York Metro area. \nCraig currently serves as a Medical Accounts Director for Novo Nordisk\, a global healthcare company with 100 years of innovation and leadership in diabetes\, obesity\, and rare disease care. Craig is responsible for providing scientific support to payers\, specialty pharmacies\, and other stakeholders that advance the care for patients living with rare diseases. \nCraig earned his Doctor of Pharmacy from St. John’s University\, and is currently based out of Queens\, NY. \n 
URL:https://hemoalliance.org/alliance-events/a-webinar-from-novo-nordisk-on-alhemo-concizumab-mtci-a-new-option-for-patients-living-with-hemophilia-a-or-b-with-inhibitors/
CATEGORIES:Members Only,Webinar
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20250417
DTEND;VALUE=DATE:20250418
DTSTAMP:20260403T172506
CREATED:20240904T140325Z
LAST-MODIFIED:20250424T135814Z
UID:68585-1744848000-1744934399@hemoalliance.org
SUMMARY:🟦 Non-Member Event : 2025 World Hemophilia Day
DESCRIPTION:Date: April 17th\, 2025 \nClick here for info.
URL:https://hemoalliance.org/alliance-events/2025-world-hemophilia-day/
CATEGORIES:Non Members
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20250423
DTEND;VALUE=DATE:20250426
DTSTAMP:20260403T172506
CREATED:20250424T134219Z
LAST-MODIFIED:20250424T134444Z
UID:70733-1745366400-1745625599@hemoalliance.org
SUMMARY:🟦 Non-Member Event : WFH 2025 Comprehensive Care Summit
DESCRIPTION:Date: April 23rd – 25th \nLocation: Dubai
URL:https://hemoalliance.org/alliance-events/non-member-event-world-federation-hemophilia/
CATEGORIES:Non Members
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20250427T183000
DTEND;TZID=America/New_York:20250429T153000
DTSTAMP:20260403T172506
CREATED:20240906T150841Z
LAST-MODIFIED:20250206T154325Z
UID:68664-1745778600-1745940600@hemoalliance.org
SUMMARY:🟥 Member Event : 2025 Nurses CE Conference
DESCRIPTION:Date: April 27 – 29\, 2025\nLocation: Orlando\, FL \n\nPlease contact Theresa Parker with any questions regarding this registration at theresa@hemoalliance.org or 727-688-2568.
URL:https://hemoalliance.org/alliance-events/2025-nurses-ce-conference/
CATEGORIES:Members Only
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20250429T183000
DTEND;TZID=America/New_York:20250501T153000
DTSTAMP:20260403T172506
CREATED:20240906T192120Z
LAST-MODIFIED:20250416T225146Z
UID:68668-1745951400-1746113400@hemoalliance.org
SUMMARY:🟥 Member Event : 2025 New HTC Staff Meeting
DESCRIPTION:Date: April 29 – May 1\, 2025\nLocation: Orlando\, FL \n\nPlease contact Theresa Parker with any questions regarding this registration at theresa@hemoalliance.org or 727-688-2568.
URL:https://hemoalliance.org/alliance-events/2025-new-htc-staff-meeting/
CATEGORIES:Members Only
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20250506T140000
DTEND;TZID=America/New_York:20250506T150000
DTSTAMP:20260403T172506
CREATED:20250418T140148Z
LAST-MODIFIED:20250421T115523Z
UID:70627-1746540000-1746543600@hemoalliance.org
SUMMARY:🟥 Member Webinar : Hemophilia Alliance Hosts - A webinar from Pfizer on Complications and challenges associated with hemophilia and a rebalancing approach with HYMPAVZI™ (marstacimab-hncq)
DESCRIPTION:Date: Tuesday\, May 6th\, 2025\nTime: 2:00pm – 3:00pm ET \n \n  \n  \n  \n  \n \nWEBINAR TOPIC: \nComplications and challenges associated with hemophilia and a rebalancing approach with HYMPAVZI™ (marstacimab-hncq) \nOBJECTIVES: \n\nEducate attendees on complications and challenges associated with hemophilia\, the novel mechanism of action of HYMPAVZI\, the BASIS Ph3 clinical trial results and dosage and administration of HYMPAVZI\nDiscuss hypothetical patients who may benefit from HYMPAVZI along with a Q&A session.\n\nSPEAKER: \n \nDr. Robert Sidonio\, Jr.\, MD\, MSc \n\n\n\n\n\n\n\nMedical Director of Hemophilia\, Medical Director of the Clinical Research Office Aflac Cancer & Blood Disorders Center Children’s Healthcare of Atlanta\nAssociate Professor of Pediatrics\, Emory University School of Medicine
URL:https://hemoalliance.org/alliance-events/a-webinar-from-pfizer-on-complications-and-challenges-associated-with-hemophilia-and-a-rebalancing-approach-with-hympavzi-marstacimab-hncq/
CATEGORIES:Members Only,Webinar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20250507T130000
DTEND;TZID=America/New_York:20250507T140000
DTSTAMP:20260403T172506
CREATED:20250429T011328Z
LAST-MODIFIED:20250429T012225Z
UID:70761-1746622800-1746626400@hemoalliance.org
SUMMARY:🟥 Member Webinar : Hemophilia Alliance Hosts - A webinar from Sanofi - Exploring data and expert perspectives on Qfitlia™ (fitusiran)
DESCRIPTION:Date: Wednesday\, May 7th\, 2025\nTime: 1:00pm – 2:00pm ET \n \n  \n  \n  \n \nWEBINAR TOPIC: \nExploring data and expert perspectives on Qfitlia™ (fitusiran) \nOBJECTIVE: \nDuring this program\, we will explore data and expert perspectives on Qfitlia™ (fitusiran)\, a newly approved prophylactic treatment for patients with hemophilia A and B\, with or without inhibitors. \nSPEAKER: \nVanessa Salinas\, MD – Center for Inherited Blood Disorders Orange\, CA \nDr. Vanessa Salinas is board certified in pediatric hematology-oncology and in general pediatrics. She completed her pediatric hematology-oncology fellowship at CHLA and completed a Coagulation and Bleeding Disorders fellowship at CHLA. She specializes in all areas of hematology with special focus in hemophilia and rare bleeding disorders\, and red cell disorders\, including sickle cell disease and thalassemia. \nDr. Salinas is interested in helping our hemophilia community and empowering our patients and families\, through education and participation. She works closely with the Hemophilia Foundation of Southern California and was awarded as the Medical Professional of the Year in 2019. Dr. Salinas participates in clinical research studies as principal investigator as well as co-investigator. Dr. Salinas advocates for children’s education\, and she enjoys nature and outdoor sports.
URL:https://hemoalliance.org/alliance-events/a-webinar-from-sanofi-exploring-data-and-expert-perspectives-on-qfitlia-fitusiran/
CATEGORIES:Members Only,Webinar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20250513T130000
DTEND;TZID=America/New_York:20250513T140000
DTSTAMP:20260403T172506
CREATED:20250418T141315Z
LAST-MODIFIED:20250509T143152Z
UID:70714-1747141200-1747144800@hemoalliance.org
SUMMARY:🟥 Member Webinar : Hemophilia Alliance Hosts - A webinar from BioMarin - A Collaborative Journey - ROCTAVIAN Patient & Provider Perspectives
DESCRIPTION:Date: Tuesday\, May 13th\, 2025\nTime: 1:00pm – 2:00pm ET \n  \n \n  \n  \n \nWEBINAR TOPIC: \nA Collaborative Journey – ROCTAVIAN Patient & Provider Perspectives \nOBJECTIVE: \nJoin us for an insightful webinar exploring the real-world experiences of patients and providers with ROCTAVIAN. Hear firsthand accounts of the treatment journey\, from initial consultations and administration to outcomes and quality of life changes. Discover how collaborative partnerships between patients and healthcare professionals are shaping the future of Hemophilia A patients. Learn about practical considerations\, clinical insights\, and the empowering potential of ROCTAVIAN. \nAUDIENCE: \nProviders and decision makers \nSPEAKERS: \n\nAndrea Buxton\, APNP\, Family Nurse Practitioner\nA patient with severe hemophilia A who has been treated with ROCTAVIAN\n\nAndrea began working as a Nurse Coordinator at the Hemophilia Outreach Center (HOC) in 2014\, and in January 2023\, she began serving as HOC’s first Family Nurse Practitioner. Since starting at HOC\, she has led several initiatives including the administration of gene therapy (both Hemgenix and Roctavian). She currently sits on the Region V-West Regional Council and Regional Gene Therapy Working Group and has served as the ATHN Community of Practice Regional Chair. Prior to her time at HOC\, she worked as an ICU nurse and hospital supervisor at St. Mary’s Hospital in Green Bay\, WI.
URL:https://hemoalliance.org/alliance-events/a-webinar-from-biomarin-a-collaborative-journey-roctavian-patient-provider-perspectives/
CATEGORIES:Members Only,Webinar
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20250514
DTEND;VALUE=DATE:20250517
DTSTAMP:20260403T172506
CREATED:20240816T142802Z
LAST-MODIFIED:20250123T220249Z
UID:68229-1747180800-1747439999@hemoalliance.org
SUMMARY:🟥 Member Event : 2025 Physical Therapists CE Conference
DESCRIPTION:Date: May 14 – 16\, 2025\nLocation: Phoenix\, AZ \n \nPlease contact Theresa Parker with any questions regarding this registration at theresa@hemoalliance.org or 727-688-2568.
URL:https://hemoalliance.org/alliance-events/member-event-2025-physical-therapists-ce-conference/
CATEGORIES:Members Only
ATTACH;FMTTYPE=image/jpeg:https://hemoalliance.org/wp-content/uploads/2024/07/previous-meetings-012.jpg
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20250519
DTEND;VALUE=DATE:20250522
DTSTAMP:20260403T172506
CREATED:20250424T134725Z
LAST-MODIFIED:20250424T134740Z
UID:70739-1747612800-1747871999@hemoalliance.org
SUMMARY:🟦 Non-Member Event : PARTNERS - Basic Partners Program for Social Workers
DESCRIPTION:Date: May 19th – 21st \nLocation: Indianapolis\, IN
URL:https://hemoalliance.org/alliance-events/non-member-event-partners-basic-partners-program-for-social-workers/
CATEGORIES:Non Members
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20250621
DTEND;VALUE=DATE:20250626
DTSTAMP:20260403T172506
CREATED:20250424T135031Z
LAST-MODIFIED:20250424T135044Z
UID:70742-1750464000-1750895999@hemoalliance.org
SUMMARY:🟦 Non-Member Event : ISTH Congress
DESCRIPTION:Date: June 21st – 25th \nLocation: Washington\, DC
URL:https://hemoalliance.org/alliance-events/non-member-event-isth-congress/
CATEGORIES:Non Members
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20250626T130000
DTEND;TZID=America/New_York:20250626T133000
DTSTAMP:20260403T172506
CREATED:20250610T183147Z
LAST-MODIFIED:20250610T183147Z
UID:70991-1750942800-1750944600@hemoalliance.org
SUMMARY:🟥 Member Webinar : Hemophilia Alliance Presents - Washington Update Webinar
DESCRIPTION:Date: Thursday\, June 26th\, 2025\nTime: 1:00pm – 2:00pm ET \n \n  \n  \n \nWEBINAR TITLE: \nWashington Update \nSESSION OBJECTIVE: \nCome to hear the latest on actions in Washington that could impact your HTC and your patients – from 340B reform and federal funding for hemophilia programs\, to Congress’ “One Big Beautiful Bill” and how it could lead to people with bleeding disorders losing their Medicaid or ACA health coverage. We’ll answer your questions and give you tools to advocate for your center and patients. \nINTENDED AUDIENCE: \nAll HTC staff \nSPEAKERS: \n\nJohanna Gray and Miriam Goldstein\, Hemophilia Alliance Federal Policy Advisors\, Artemis Policy Group\nDean Hindenlang\, PhD\, Hemophilia Alliance Vice Chair\n\n  \n \nJohanna Gray serves the Hemophilia Alliance as a federal policy advocacy consultant. She has more than a decade of experience in health policy and government relations\, working with clients to develop and implement successful advocacy strategies involving Congress and federal public health agencies. Johanna’s clients include patient advocacy groups\, physician specialty societies\, and associations of specialized treatment centers. \nJohanna’s expertise in health policy ranges from the broadly applicable private insurance market reforms included in the Affordable Care Act (ACA) to the specifics of Medicare reimbursement for particular physician services. During the ACA negotiations\, Johanna led a coalition of seventy patient advocacy groups and other supporters\, which successfully advocated for the elimination of lifetime limits on private health insurance in the law. \nHaving began her career as an intern for then-Senator Barack Obama\, Johanna held several policy analysis and advocacy positions before joining CRD. Johanna received a Master of Public Administration and Certificate in Health Services Management and Policy from the Maxwell School at Syracuse University and a B.A. in Public Policy Studies with honors from the University of Chicago. \n \nMiriam Goldstein joined the Artemis Policy Group as a Senior Policy Advisor in August 2024 after more than seven years at Hemophilia Federation of America. Miriam focuses on federal and state policies impacting patient access to coverage\, access to care\, and affordability. Over the course of her legislative and regulatory work\, Miriam has developed expertise in the Affordable Care Act and insurance reform\, Medicaid eligibility and program requirements; and other keystones of the health policy landscape. \nBefore her time at HFA\, Miriam worked as an attorney in private practice and with the US Securities and Exchange Commission. Miriam earned her J.D. degree from the University of Pennsylvania and her B.A. in history from Yale. She is admitted to practice law in D.C. Miriam lives in Arlington\, Virginia\, and in her free time can often be found cycling on local bike trails with her husband Dave. \n \nDean M. Hindenlang has served the nonprofit and government sectors for almost 30 years\, focusing on strategic planning\, administrative oversight and governance\, and coalition-building through an equity-based lens. As Director of Public Policy and Strategic Initiatives with Cascade Hemophilia Consortium\, his work focuses on coalition-building while helping ensure that individuals needing assistance are advocated for in community and government-based capacities. He is a proven leader in assisting members of marginalized and underserved communities. \nMr. Hindenlang holds a Ph.D. in Public Policy and Administration\, completing his doctoral dissertation on equity in community-based programming. He has a Master of Public Administration\, a Master of Science in Marketing and Communication\, a Master of Healthcare Administration\, and a bachelor’s degree in English. Additionally\, he serves as an adjunct professor\, doctoral faculty methodologist\, and subject matter expert at Franklin University. He also offers undergraduate instruction on social justice and cultural awareness at Southern New Hampshire University. \nAs the Director of Public Policy and Strategic Initiatives\, Dean serves Cascade HC by engaging local and state authorities\, as well as elected officials\, on matters of public policy actions\, projects\, and patient education and advocacy.
URL:https://hemoalliance.org/alliance-events/june-2025-washington-update-webinar/
CATEGORIES:Members Only
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20250716
DTEND;VALUE=DATE:20250718
DTSTAMP:20260403T172506
CREATED:20250424T135306Z
LAST-MODIFIED:20250424T140053Z
UID:70745-1752624000-1752796799@hemoalliance.org
SUMMARY:🟦 Non-Member Event : PARTNERS - Basic Partners Program for Non Clinical and Administrative
DESCRIPTION:Date: July 16th – 17th \nLocation: Indianapolis\, IN
URL:https://hemoalliance.org/alliance-events/non-member-event-partners-basic-partners-program-for-non-clinical-and-administrative/
CATEGORIES:Non Members
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20250722T130000
DTEND;TZID=America/New_York:20250722T140000
DTSTAMP:20260403T172506
CREATED:20250707T164147Z
LAST-MODIFIED:20250708T150629Z
UID:71108-1753189200-1753192800@hemoalliance.org
SUMMARY:🟥 Member Webinar : Hemophilia Alliance Hosts - A webinar from Octapharma - Review The Clinical Benefits of wilate®\, Highlighting The Benefits vs Current vWD Therapies
DESCRIPTION:Date: Tuesday\, July 22nd\, 2025\nTime: 1:00pm – 2:00pm ET \n  \n \n  \n  \n  \n \nWEBINAR TOPIC: \nReview the clinical benefits of wilate®\, highlighting the benefits vs current vWD therapies. \nOBJECTIVES: \n\nUnderstand the attributes of wilate® for vWD: 1:1 ratio which mimics the physiologic activity of vWF and FVIII and the synchronous decay curves\, which facilitates factor activity monitoring.\nUnderstand the absence of vWF or FVIII accumulation when using wilate® during surgery and prophylaxis.\nReview the only product approved for children older than 6 years and adults with any type of vWD and under any clinical circumstance.\n\nAUDIENCE: \nAll HTC Staff \nSPEAKER: \nClaudio Sandoval\, Senior Director of Scientific & Medical Affairs at Octapharma \nClaudio Sandoval is the Senior Director of Scientific & Medical Affairs at Octapharma. Before his current role he was a pediatric hematologist-oncologist for 30 years caring for children with bleeding disorders\, cancer\, sickle cell disease\, and other maladies. Claudio graduated from New York Medical College and trained at Schneider Children’s Hospital in New Hyde Park\, NY and St. Jude Children’s Research Hospital in Memphis\, TN.
URL:https://hemoalliance.org/alliance-events/a-webinar-from-octapharma-review-the-clinical-benefits-of-wilate-highlighting-the-benefits-vs-current-vwd-therapies/
CATEGORIES:Members Only,Webinar
ATTACH;FMTTYPE=image/png:https://hemoalliance.org/wp-content/uploads/2024/06/Octapharma-logo-blue.png
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20250812T130000
DTEND;TZID=America/New_York:20250812T140000
DTSTAMP:20260403T172506
CREATED:20250804T120753Z
LAST-MODIFIED:20250804T120753Z
UID:71288-1755003600-1755007200@hemoalliance.org
SUMMARY:🟥 Member Webinar : Hemophilia Alliance Presents - Big Bill\, Big Insurance Impact Webinar
DESCRIPTION:Date: Tuesday\, August 12th\, 2025\nTime: 1:00pm – 2:00pm ET \n \n  \n  \n \nWEBINAR TITLE: \nBig Bill\, Big Insurance Impact – What do HTCs need to know now about coming health insurance changes and how to prepare? \nSESSION OBJECTIVE: \nThe One Big Beautiful Bill Act and other Washington policies are reshaping the insurance landscape for HTCs and their patients with Medicaid and ACA coverage\, starting as soon as later this month! Please join The Hemophilia Alliance for this essential new webinar series\, kicking off with a comprehensive overview of the coming policy changes. We will also provide strategies for HTCs to start to prepare and advocate to help patients maintain vital coverage. Future sessions will tackle specific policy and HTC operational challenges in detail. \nINTENDED AUDIENCE: \nAll HTC staff \nSPEAKERS: \nJohanna Gray\, Hemophilia Alliance Federal Policy Advisors\, Artemis Policy Group \n \nJohanna Gray serves the Hemophilia Alliance as a federal policy advocacy consultant. She has more than a decade of experience in health policy and government relations\, working with clients to develop and implement successful advocacy strategies involving Congress and federal public health agencies. Johanna’s clients include patient advocacy groups\, physician specialty societies\, and associations of specialized treatment centers. \nJohanna’s expertise in health policy ranges from the broadly applicable private insurance market reforms included in the Affordable Care Act (ACA) to the specifics of Medicare reimbursement for particular physician services. During the ACA negotiations\, Johanna led a coalition of seventy patient advocacy groups and other supporters\, which successfully advocated for the elimination of lifetime limits on private health insurance in the law. \nHaving began her career as an intern for then-Senator Barack Obama\, Johanna held several policy analysis and advocacy positions before joining CRD. Johanna received a Master of Public Administration and Certificate in Health Services Management and Policy from the Maxwell School at Syracuse University and a B.A. in Public Policy Studies with honors from the University of Chicago.
URL:https://hemoalliance.org/alliance-events/member-webinar-hemophilia-alliance-presents-big-bill-big-insurance-impact-webinar/
CATEGORIES:Members Only,Webinar
END:VEVENT
BEGIN:VEVENT
DTSTART;VALUE=DATE:20250821
DTEND;VALUE=DATE:20250824
DTSTAMP:20260403T172506
CREATED:20250424T135500Z
LAST-MODIFIED:20250424T135518Z
UID:70748-1755734400-1755993599@hemoalliance.org
SUMMARY:🟦 Non-Member Event : NBDF BDC
DESCRIPTION:Date: August 21st – 23rd \nLocation: Denver\, CO
URL:https://hemoalliance.org/alliance-events/non-member-event-nbdf-bdc/
CATEGORIES:Non Members
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20250827T140000
DTEND;TZID=America/New_York:20250827T150000
DTSTAMP:20260403T172506
CREATED:20250811T132405Z
LAST-MODIFIED:20250811T134758Z
UID:71300-1756303200-1756306800@hemoalliance.org
SUMMARY:🟥 Member Webinar : Hemophilia Alliance Hosts - A Webinar From Pfizer On Subcutaneous HYMPAVZI (marstacimab-hncq): Learn More From a Real-World Patient Experience
DESCRIPTION:Date: Wednesday\, August 27th\, 2025\nTime: 2:00pm – 3:00pm ET \n  \n \n  \n  \n  \n  \n \nWEBINAR TITLE: \nJuggling Fall Routines Can Be Complicated. Help your patients keep their hemophilia treatment simple with subcutaneous HYMPAVZI (marstacimab-hncq): Learn More From a Real-World Patient Experience. \nOBJECTIVES: \nTo educate attendees on challenges\, shared decision making in hemophilia and introduce HYMPAVZI pen\, dosage\, administration\, and real-world patient experience with HYMPAVZI. \nAUDIENCE: \nAll HTC Staff\, Physicians\, Nurses\, Pharmacists\, etc. \nSPEAKER: \nSteven Pipe\, MD. \nDr. Steven Pipe is a Professor and the Laurence A. Boxer Research Professor of Pediatrics and Professor of Pathology at the University of Michigan\, Ann Arbor\, Michigan\, USA. He is the medical director of the Pediatric Hemophilia and Coagulation Disorders Program and medical director of the Special Coagulation Laboratory. His clinical interests include bleeding and thrombotic disorders and congenital vascular anomalies. Dr Pipe also directs a basic research lab investigating coagulation factor VIII and the molecular mechanisms of hemophilia A. He has been actively involved in clinical trials with novel therapeutics for hemophilia including gene therapy. He was the 2015 recipient of the Leadership in Research Award from the National Hemophilia Foundation. He has served on the Board of Directors for the Hemostasis and Thrombosis Research Society\, as Chair of the Board of Directors for the American Thrombosis and Hemostasis Network and most recently as Chair of the Medical and Scientific Advisory Council to the National Hemophilia Foundation.
URL:https://hemoalliance.org/alliance-events/a-webinar-from-pfizer-on-subcutaneous-hympavzi-marstacimab-hncq-learn-more-from-a-real-world-patient-experience/
CATEGORIES:Members Only,Webinar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20250904T130000
DTEND;TZID=America/New_York:20250904T140000
DTSTAMP:20260403T172506
CREATED:20250820T205915Z
LAST-MODIFIED:20250820T210018Z
UID:71357-1756990800-1756994400@hemoalliance.org
SUMMARY:🟥 Member Webinar : Hemophilia Alliance Hosts - A Webinar From BioMarin On Advancing Care with ROCTAVIAN® (valoctocogene roxaparvovec-rvox): Clinical Evidence\, Patient Perspective & Contract Opportunities
DESCRIPTION:Date: Thursday\, September 4th\, 2025\nTime: 1:00pm – 2:00pm ET \n  \n \n  \n  \n \nWEBINAR TITLE: \nAdvancing Care with ROCTAVIAN® (valoctocogene roxaparvovec-rvox): Clinical Evidence\, Patient Perspective & Contract Opportunities. \nOBJECTIVES: \n\nExplore updates to HEM Alliance member contract terms and the associated provider economics.\nReview the latest clinical data updates\, describing the long-term efficacy and safety of ROCTAVIAN.\nHear a firsthand experience from a patient who has received ROCTAVIAN\, offering valuable insights into the real-world impact of this therapy.\n\nAUDIENCE: \nAll HTC Staff. \nSPEAKERS: \n\nDawn St Amand\, Associate Director\, BioMarin Medical Science Liaison Hemophilia\nSophie Synder\, Director\, BioMarin US Value and Access\nAndrew W.\, ROCTAVIAN Patient Experience
URL:https://hemoalliance.org/alliance-events/a-webinar-from-biomarin-on-advancing-care-with-roctavian-valoctocogene-roxaparvovec-rvox-clinical-evidence-patient-perspective-contra/
CATEGORIES:Members Only,Webinar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20250910T130000
DTEND;TZID=America/New_York:20250910T140000
DTSTAMP:20260403T172506
CREATED:20250827T014952Z
LAST-MODIFIED:20250827T020613Z
UID:71370-1757509200-1757512800@hemoalliance.org
SUMMARY:🟥 Member Webinar : Hemophilia Alliance Hosts - A Webinar From BD SUMHAC - Mental Health and Substance Use in the Bleeding Disorders Community
DESCRIPTION:Date: Wednesday\, September 10th\, 2025\nTime: 1:00pm – 2:00pm ET \n \n  \n  \n  \n  \n \nWEBINAR TITLE: \nMental Health and Substance Use in the Bleeding Disorders Community. \nDESCRIPTION: \nThe bleeding disorders community does not have the same access to inpatient and residential mental health and substance use treatment that the general population does. This webinar will talk about the barriers to access the BD community faces and the strategies and resources available to support HTC providers in addressing their patients’ mental health and substance use needs. It will also encourage HTC providers to ask their patients about mental health and substance use concerns early and often and advocate on their behalf when necessary.  \nOBJECTIVES: \n\nTo describe the mental health and substance use needs of the bleeding disorders community.\nTo outline the barriers to inpatient and residential mental health and substance use treatment the bleeding disorders community .\nTo provide data demonstrating that HTC provider advocacy on behalf of patients can overcome barriers to access.\nTo share tools and resources to support your patients’ behavioral health journey and assist in getting people with bleeding disorders access to mental health and substance use care. \n\nAUDIENCE: \nAll HTC Providers. \nSPEAKERS: \nKate Bazinsky\, MPH. \nKate Reinhalter Bazinsky has spent over two decades working in health policy and advocacy at the federal\, state\, and local levels. When her son was diagnosed with severe hemophilia A\, she became a passionate advocate for the bleeding disorders community. She co-founded and now serves as the Chair of the Bleeding Disorders Substance Use & Mental Health Access Coalition (BD SUMHAC). BD SUMHAC is a national\, multi-stakeholder coalition committed to ensuring equitable access to appropriate substance use and mental health treatment facilities for all individuals with bleeding disorders\, with a focus on inpatient and residential facilities. Kate has a Master of Public Health from Johns Hopkins University\, She lives in Wellesley\, MA with her husband and two children. \n \nLucy Ramirez\, LCSW. \nLucy Ramirez is a licensed clinical social worker for the Rush Hemophilia and Thrombophilia Treatment Center at the Rush University Medical Center in Chicago\, Illinois. In her current position\, Ms. Ramirez’s practice primarily involves counseling and educating individuals with bleeding disorders\, their caregivers and family members. She has served as facilitator and guest speaker for patient educational events sponsored by the National Bleeding Disorders Foundation\, the Bleeding Disorder Alliance of Illinois\, the VWD Connect Foundation and the Coalition for Hemophilia B. She serves as the current vice chair of the National Bleeding Disorders Foundation’s Social Work Working Group.
URL:https://hemoalliance.org/alliance-events/a-webinar-from-bd-sumhac-mental-health-and-substance-use-in-the-bleeding-disorders-community/
CATEGORIES:Members Only,Webinar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20250917T140000
DTEND;TZID=America/New_York:20250917T150000
DTSTAMP:20260403T172506
CREATED:20250908T140351Z
LAST-MODIFIED:20250912T145220Z
UID:71498-1758117600-1758121200@hemoalliance.org
SUMMARY:🟥 Member Webinar : Hemophilia Alliance Hosts - A Webinar From Sanofi - Qfitlia Overview - Clinical\, Access\, and Distribution Dynamics
DESCRIPTION:Date: Wednesday\, September 17th\, 2025\nTime: 2:00pm – 3:00pm ET \n \n  \n  \n  \n \nWEBINAR TOPIC: \nQfitlia Overview: Clinical\, Access\, and Distribution Dynamics. \nOBJECTIVE: \nDr. Lynn Malec will review key elements of the Qfitlia efficacy and safety profile and Adam Gurry\, Sanofi Director of Access Strategy\, will provide insights on the Qfitlia access and distribution strategy. \nAUDIENCE: \nAll HTC Providers and Staff. \nSPEAKERS: \n\nLynn Malec\, MD. received her undergraduate and medical school degrees from the University of Wisconsin\, and went on to complete a residency in Internal Medicine and Pediatrics followed by a Pediatric Hematology/Oncology fellowship at the University of Pittsburgh/Children’s Hospital of Pittsburgh. Currently\, Dr. Malec is an Associate Investigator at the Versiti Blood Research Institute and Assistant Professor of Medicine and Pediatrics at the Medical College of Wisconsin. Dr. Malec serves as the Medical Director of the Comprehensive Center for Bleeding Disorders at Versiti. She is actively engaged in the care and research involving both adults and children with hemophilia and other bleeding and clotting disorders; her specific area of clinical research is focused on inhibitors in hemophilia and the impact of new factor products.\nAdam Gurry\, Director of Access Strategy at Sanofi has 19 years of experience on the commercial side of the business holding various roles of increasing responsibility. The past 5 years Adam has been focused on the Rare Blood therapeutic area responsible for the development of payer facing marketing materials and recently led the development of Qfitlia’s access strategy.
URL:https://hemoalliance.org/alliance-events/a-webinar-from-sanofi-qfitlia-overview-clinical-access-and-distribution-dynamics/
CATEGORIES:Members Only,Webinar
END:VEVENT
BEGIN:VEVENT
DTSTART;TZID=America/New_York:20251001T130000
DTEND;TZID=America/New_York:20251001T140000
DTSTAMP:20260403T172506
CREATED:20250912T142319Z
LAST-MODIFIED:20250912T143403Z
UID:71518-1759323600-1759327200@hemoalliance.org
SUMMARY:🟥 Member Webinar : Hemophilia Alliance Hosts - A Webinar From Takeda - On-demand and Surgical Use of ADVATE® [Antihemophilic Factor (Recombinant)]
DESCRIPTION:Date: Wednesday\, October 1st\, 2025\nTime: 1:00pm – 2:00pm ET \n \n  \n  \n  \n \nWEBINAR TOPIC: \nOn-demand and Surgical Use of ADVATE® [Antihemophilic Factor (Recombinant)] \nOBJECTIVE: \nThis session will explore critical aspects of hemophilia A management\, focusing on the unique role of ADVATE in on-demand and perioperative settings. \nAUDIENCE: \nAll HTC Staff. \nSPEAKER: \nJessica Grandoni\, Pharm.D.\, BCPS\, was the Hemostatic Antithrombotic Stewardship Lead Pharmacist (HAT)\, and clinical pharmacy specialist\, at Brigham and Women’s Hospital in Boston\, Massachusetts. She is now a clinical pharmacy specialist at the Dana Farber Cancer Institute’s Anticoagulation Management Service. \nJessica has been involved in several committees and initiatives related to her practice interests of anticoagulation therapy and reversal\, heparin induced thrombocytopenia\, mechanical circulatory support\, drug formulary management and associated guidelines. She is involved in research\, education\, and publications with pharmacy\, hematology\, cardiology\, and the mechanical circulatory support division. She has published one of the top downloaded articles with the American Journal of Hematology and has presented at national and international conferences. Jessica earned her Doctor of Pharmacy degree from Massachusetts College of Pharmacy and Health Sciences University in Boston and completed an ASHP-accredited Post Graduate Year 1 residency at Beth Israel Deaconess Medical Center. She also completed an ASHP-accredited Post Graduate Year 2 cardiology residency at The University of California Davis Medical Center with a focus in anticoagulation and reversal.
URL:https://hemoalliance.org/alliance-events/a-webinar-from-takeda-on-demand-and-surgical-use-of-advate-antihemophilic-factor-recombinant/
CATEGORIES:Members Only,Webinar
END:VEVENT
END:VCALENDAR