Spotlight Sessions are thought leadership opportunities at AMCP national meetings offered in 15-minute, 30-minute, and 60-minute
The RWE Arena and Spotlight Stage are located in Hall B in the Music City Center and include programming on Tuesday, April 14 from 11am-5:15pm and on Wednesday, April 15 from 9:30am-2:30pm.
Additional program details and faculty information can be found on the AMCP 2026 mobile app, available at the end of March.
Tuesday, April 14 | 11-11:30am | The Spotlight Stage
Precision Medicine Isn’t Precise Without Testing
Behind every targeted therapy is a testing journey that too often falls apart. This spotlight explores where patients fall through the cracks—and how AMCP’s Precision Medicine Initiative is bringing stakeholders together to close the gaps and get precision medicine right. From inconsistent terminology to misaligned coverage decisions, precision medicine can get lost in translation. Learn how AMCP is simplifying the conversation and creating practical tools to support clearer, more consistent biomarker testing access.
Brought to you by AMCP
Tuesday, April 14 | 11-11:30am | RWE Arena
Real-World Identification of Obesity: Development and Internal Validation of a Claims-Based Machine Learning Algorithm
This study addresses a practical managed care evidence gap: obesity is substantially under-identified in claims when relying on diagnosis codes alone. Using a large linked real-world dataset of commercial and Medicare Advantage claims enriched with EHR BMI, labs, and area-level SDOH, the investigators developed a machine-learning algorithm to identify obesity more accurately. The key message is that the model showed clear improvement over diagnosis codes alone, with materially higher sensitivity and strong overall discrimination, while maintaining reasonable specificity and PPV. This makes the work highly relevant for payer analytics, outcomes research, population health management, and targeting obesity-related interventions when BMI is not directly available in claims.
Featuring:
Hiangkiat (Jason) Tan, BSPharm, MS
Senior Research Scientist
Carelon Research
Brought to you by AMCP Research Institute
Tuesday, April 14 | 11:45am-12:30pm | The Spotlight Stage
Optimizing the Treatment of Chronic Hand Eczema in Managed Care
Join Us for a Critical Update on Chronic Hand Eczema Management
This session will provide an overview of Chronic Hand Eczema (CHE) and considerations for its management within managed care settings.
The presentation will include a discussion of recent research efforts, including CHECK-US and RWEAL-US, as well as evolving perspectives on treatment approaches and unmet needs in CHE.
Attendees will also hear from a panel of experts representing health economics, clinical practice, and managed care, who will share insights on current challenges, treatment pathways, and considerations for care delivery.
This session is intended for stakeholders involved in formulary decision-making, specialty pharmacy management, and care pathway development, and will offer an opportunity to engage with emerging data and expert perspectives in CHE management.
Featuring:
Diana Brixner, RPh, PhD, FAMCP
Professor Emeritus, University of Utah
Principal, Millcreek Outcomes Group
Suzan Tsang, PharmD
Director, Medical Outcomes
LEO Pharma
Aseel Bin Sawad, PharmD, MSc, MCR, MS, PhD, DBA
AD, Health Care Systems & HEOR
LEO Pharma
Jeff Dunn, PharmD, MBA
Chief Clinical Officer,
Cooperative Benefits Group
Sponsored by: LEO Pharma
Tuesday, April 14 | 12:30-12:45pm | RWE Arena
Static to Strategic: Leveraging Innovative eModels to Navigate Complex Payer Negotiations
Join Keshia Maughn, Senior Principal at STATinMED, & Damian M. May, Managing Director, Chrysoli Consulting for a fast-paced, highly interactive 15-minute session designed to reflect the real-world constraints of payer engagement conversations.
This session moves beyond the traditional presentation format and delivers a live demonstration of innovative eModel technology—showing how compliant, interactive budget impact tools can transform complex real-world evidence into clear, compelling narratives that support payer negotiations.Keshia & Damian will demonstrate how modern eModels can enable teams to deliver strategic, decision-ready insights in minutes helping stakeholders visualize cost drivers, scenario outcomes, and value tradeoffs in a way that is both transparent and impactful.
The demonstration will be followed by a brief, high-impact discussion with industry experts, offering candid perspectives on the challenges and opportunities of using interactive evidence tools to support field engagement and payer decision-making.
Attendees will gain practical insight into how interactive budget impact eModels can reduce information overload, strengthen value communication, and elevate payer discussions from static reporting to strategic dialogue. This session is ideal for market access, HEOR, RWE, and evidence strategy professionals looking to modernize how they communicate value and improve outcomes in high-stakes formulary conversations.
Featuring:
Keshia Maughn, MPH
Senior Principal of Strategic Advisory Services
STATinMED
Damian M. May, PharmD, MBA
Managing Director & Executive Principal Consultant
Chrysoli Consulting
Sponsored by: STATinMED
Tuesday, April 14 | 12:45-1:15pm | The Spotlight Stage
How Misaligned Incentives and Organizational Agendas Derail Healthcare
Featuring:
John Guarino
Chairman Emeritus, Market Access
Klick Health
Sponsored by: Klick
Tuesday, April 14 | 1-1:30pm | RWE Arena
Optimizing Managed Care with Real-World Data: Insights into Safety, Efficacy, and Access
Real-world data has become a cornerstone of modern healthcare innovation, with its true value emerging when transformed into real-world evidence. These actionable insights help shape decision-making across the life sciences ecosystem. This session explores the journey from data to evidence, showcasing how diverse RWD sources are driving advancements in drug development, disease understanding, and health care delivery.
Featuring:
Audrey Djibo, MS, PhD
Lead Director - Epidemiology & Science
CVS Healthspire Life Science Solutions
Natasha Oyedele, MPH, PhD
Lead Epidemiologist
CVS Healthspire Life Sciences Solutions
Joaquim Fernandes, MS
Executive Director – Research and Analytics
CVS Healthspire Life Sciences Solutions
Brought to you by AMCP Research Institute
Tuesday, April 14 | 1:30-2pm | The Spotlight Stage
Not all Obesity is the Same - Perspectives for Managed Care
The melanocortin 4 receptor (MC4R) pathway is critical for satiety and energy balance regulation. Impairment in the MC4R pathway can be caused by genetic variants or hypothalamic injury and is associated with a number of rare forms of obesity. These neuroendocrine diseases are characterized by weight gain, reduced energy expenditure, and hyperphagia and carry significant, long-term burdens for patients and their caregivers. This presentation will review several diseases caused by MC4R pathway impairment as well as approved therapy.
Faculty:
JB Collins, Medical Science Liaison
Sponsored by: Rhythm Pharmaceuticals
Tuesday, April 14 | 1:45-2pm | RWE Arena
Advancing Payer Communication with Real-World Evidence: A Fresh Look at FDA’s HCEI Guidance
FDA’s HCEI guidance is the primary guidance for industry on communicating healthcare economic information to payors, formulary committees, and other similar entities in the United States. This presentation will provide a high-level overview of the guidance and explore how the growing role of RWE may create new opportunities—and new questions—for payer communication, including where it may prompt renewed discussion of foundational concepts such as economic consequence.
Audience takeaway:
Attendees will leave with a clearer understanding of FDA’s HCEI guidance and a broader perspective on how RWE may create new opportunities and new questions in payer communication.
Featuring:
Vishvas Garg
Senior Director, Global Innovative Evidence and RWD
AbbVie
Sponsored by: AbbVie
Tuesday, April 14 | 2-2:15pm | The Spotlight Stage
Identifying Resistance Before Progression: Real‑World Evidence on ESR1 Mutations in ER+/HER2- aBC
Emergence of estrogen receptor 1 mutations (ESR1m) is a recognized driver of resistance to aromatase inhibitors in ER+/HER2‑ advanced breast cancer, yet how this resistance unfolds and is managed in real‑world practice is less well characterized. This presentation will explore real‑world outcomes among patients undergoing first‑line therapy who were tested for ESR1 mutations in U.S. community oncology settings. In addition to covering real-world outcomes of ESR1 mutations that emerge prior to disease progression, we will review how clinicians respond in routine practice, and what these patterns may suggest about opportunities for more personalized and proactive treatment decision‑making.
Brought to you by AMCP and AstraZeneca
Tuesday, April 14 | 2:15-2:30pm | RWE Arena
From Data to Decisions: Translating Real World Data into Actionable Insights for Better Healthcare Decision Making
This session will demonstrate how connected data across pharmacy, medical, and clinical settings enables precise patient targeting to power research and generate actionable insights. Through real examples, attendees will see how these insights are translated into healthcare decisions that impact outcomes, access, and cost-of-care decisions.
Featuring:
Chakita Williams, PhD.
Head of Business Development and Research Partnerships
CVS Healthspire™ Life Sciences Research
Sponsored by: CVS Healthspire
Tuesday, April 14 | 2:45-3pm | The Spotlight Stage
Enhancing Skin Confidence and Quality in the GLP-1 User Journey with a Topical Hyaluronic Acid Regimen
While GLP-1 therapies target metabolic health, many patients report self-perceived skin changes such as intense dryness, loss of plumpness, and loss of elasticity. The impact of a high-performance Hyaluronic Acid and Vitamin B5 regimen was assessed on the skin quality of 112 patients prescribed GLP-1 medications for weight loss. Following the 4-week regimen, 94% of subjects reported that the products effectively addressed their specific skin concerns since starting their medication. These results demonstrate a dermocosmetic regimen can provide a meaningful support system, effectively addressing the skin transitions and quality-of-life needs of patients on GLP-1 therapy.
Featuring:
Stephanie Laga, PhD
Scientific Liaison, Research & Innovation
L’Oréal
Sponsored by: L’Oreal
Tuesday, April 14 | 2:45-3:15pm | RWE Arena
Understanding recent self-reported biosimilar use among individuals with IBD
This presentation will provide preliminary data from an ongoing qualitative research study being conducted by Carelon Research and BBCIC. We will describe how self-reported biosimilar use captured in surveys and interviews aligns with biosimilar documentation in medical claims among individuals with IBD. Reasons for misalignment between the two sources and implications for future survey research on biosimilars will be discussed.
Featuring:
Sarah Daugherty, PhD, MPH
Principal Scientist
Carelon Research
Brought to you by BBCIC
Tuesday, April 14 | 3:15-3:45pm | The Spotlight Stage
The Wake-up Call: AMCP National Insights to Regional Action for Idiopathic Hypersomnia
A physician living with Idiopathic Hypersomnia (IH) opens this session by sharing a clinical and personal perspective on the challenges of the disease. Their narrative anchors national AMCP Market Insights findings on diagnostic barriers and coverage criteria, showing how these challenges manifest for both providers and patients. The session then details how a regional payer-provider collaborative translated these insights into action, focusing on early recognition in primary care, specialist referral pathways, and the nuances of provider attestation.
Brought to you by AMCP
Tuesday, April 14 | 3:30-4:30pm | RWE Arena
Research Podium Session – Leveraging Real-World Data to Advance Managed Care Pharmacy Practice
Each year, hundreds of authors submit research abstracts to AMCP’s Annual Meeting. Accepted abstracts are presented as posters in the Expo Hall and published in a special issue of the Journal of Managed Care + Specialty Pharmacy. Four top abstracts are awarded platinum ribbons and presented at the Research Podium Session.
The platinum abstract award presentations are:
1. GLP-1RA vs. SGLT-2i: preventing kidney function deterioration among patients with type 2 diabetes and chronic kidney disease
2. Characteristics associated with nonadherence from data collected as part of an automated refill reminder program
3. Impact of the Illinois biomarker testing law on utilization in advanced non-small cell lung cancer (aNSCLC) and metastatic colorectal cancer (mCRC) patients
4. Out-of-Pocket (OOP) Cost Burden for Prescription Drugs: Trends and Disparities in Commercial Insurance Design
Moderator:
Laura E. Happe, PharmD, MPH, FAMCP, Editor-in-Chief, Journal of Managed Care + Specialty Pharmacy
Featuring:
Liang-Yuan (Claire) Lin
PhD Candidate, Department of Pharmacy Administration
University of Mississippi
James Chamberlain, PharmD, MS
Health Economics & Outcomes Manager
MedImpact
Stella Ko, PharmD, MS
Health Economist
Genentech
Ulrich Neumann, MBA, MSc, MA
Director, Center for Healthcare Policy Research
Johnson & Johnson
Brought to you by AMCP Research Institute
Wednesday, April 15 | 9:30-9:45am | The Spotlight Stage
Eye on the Future: Exploring the Latest Payer Trends in Cell and Gene Therapies and Anti-Obesity Medications
Join us for a session exploring the evolving US payer landscape for cell and gene therapies (CGTs) and anti-obesity medications (AOMs). This discussion will focus on how payers are addressing access and formulary management within managed care organizations, providing actionable insights for stakeholders across the healthcare ecosystem.
Attendees will gain exclusive insights from two recent Cencora studies featuring perspectives from decision-makers at health plans, pharmacy benefit managers (PBMs), and integrated delivery networks (IDNs). These studies shed light on the current and future state of coverage, utilization management, and payer expectations for these innovative therapies.
Key topics will include:
• Current payer coverage trends for CGTs and AOMs, including formulary placement strategies
• Utilization management tools being applied to manage access and costs
• The types of data and evidence payers prioritize when evaluating new therapies
• Payer perspectives on the future outlook for CGTs and AOMs, including anticipated challenges and opportunities
By the end of this session, participants—particularly those from biopharmaceutical manufacturers and managed care organizations—will leave with a deeper understanding of the latest payer trends and practical insights to navigate the evolving access and formulary landscape for these transformative therapies.
Featuring:
Shaila Yoshida
Assistant Director, Value and Access Strategy
Cencora
Sponsored by: Cencora
Wednesday, April 15 | 10-10:30am | The Spotlight Stage
Did you know? The Behind‑the‑Scenes Forces Shaping Our Work
Ever wonder who decides what an ICD‑10 code is — or how in the world do patients get access to therapies before they’re approved in a country? In this “Did You Know?” session, we’ll unpack two behind-the-scenes topics that have a real impact on evidence, policy, access, and day-to-day business decisions.
First, we’ll explore how ICD‑10 codes evolve over time and why those updates can have a meaningful ripple effect across coverage, evidence, and day-to-day decision-making. Then we’ll shift to global early access programs highlighting global access pathways that exist, in the US, EU and other global markets, for both compassionate use and named patient sales. Understanding these pathways, patient populations that can be accessed, and the nuanced regulatory language in these markets, can provide an opportunity to connect patients in need to innovative therapies, otherwise unavailable in many global markets.
We’ll keep it practical, interactive, and focused on what these processes mean for real-world work.
Brought to you by AMCP
Wednesday, April 15 | 10:30-11am | RWE Arena
Delivering Relevant and Reliable Real-World Evidence to Support Medicare Drug Price Negotiations
As the U.S. Centers for Medicare and Medicaid Services (CMS) implements the Medicare Drug Price Negotiation Program under the Inflation Reduction Act (IRA), a key challenge is ensuring that price determinations are informed, in a transparent manner, by high-quality, relevant evidence on how selected drugs perform in the Medicare population. While CMS has made meaningful strides in articulating how it will assess clinical benefit and comparative effectiveness, greater clarity is needed—particularly regarding the use and interpretation of real-world evidence (RWE) as part of the negotiation process. How CMS should assess RWE during price negotiations and actively shape upstream evidence generation through clearer expectations and guidance? This session will provide professional and up-to-date perspectives on relevant work published to date and how CMS can offer manufacturers and other stakeholders effective signals and pathways to reduce uncertainty around evidence expectations.
Featuring:
Rachele Hendricks-Sturrup, DHSc, MSc, MA
Research Director
Duke-Robert J. Margolis Institute for Health Policy
Brought to you by AMCP Research Institute
Wednesday, April 15 | 10:45-11:30am | The Spotlight Stage
Impact of ADA 2026 Guidelines on Patient Care and Metabolic Health: Operational Strategies for Managed Care Professionals
Learning Objectives:
- Define the scope and drivers of the metabolic health crisis in the United States and its implications for patients and the healthcare system.
- Summarize key updates from the 2026 American Diabetes Association Standards of Care in Diabetes and their impact on clinical practice.
- Explore managed care strategies that support improved metabolic health outcomes across populations.
Brought to you by AMCP and sponsored by Dexcom
Wednesday, April 15 | 11-11:30am | RWE Arena
Designing Real World Evidence Studies: The Regulatory Landscape
Real World Evidence (RWE) is rapidly reshaping decisions across the FDA, payers, and healthcare, but how can you actually design RWE studies that meet regulatory requirements, mitigate bias, and present high-quality findings? Unpacking the evolving U.S. regulatory landscape must begin by reviewing the history of the FDA and RWE and the resulting guidance ranging from FDAMA §114 to HIPAA to FDA Study Design. Current guidance specifies how to build RWE protocols, reduce risk and ensure de-identification for patients, and establish that evidence is "fit-for-purpose" for the question at hand. In addition, transparency, harmonization of data elements, adjustment for common biases, and methods to prevent potential misapplication of findings are covered. This presentation will mix ethical considerations with sound research design with the past, present, and potential future of RWE regulation in the United States.
Featuring:
Kevin Kallmes
Chief Executive Officer and Co-Founder
Nested Knowledge, Inc.
Brought to you by AMCP Research Institute
Wednesday, April 15 | 11:45am-12:15pm | The Spotlight Stage
Introducing a New Standard for Payer Drug Evaluation: The Payer Value Index (PVI) in Collaboration with AMCP
The AMCP Format standardized how manufacturers communicate evidence to payers and is now widely adopted across the industry. Today, AMCP and the Payer Value Index (PVI) are introducing a new approach for how payers and healthcare decision-makers evaluate drug value—through an independent, transparent, and payer-centric methodology.
In this session, we will demonstrate how PVI works and how it supports structured evidence and value assessment across clinical, economic, and patient-centered dimensions. We will also show how PVI analyses are integrated into payer-centric AMCP eModels to enable plan-specific economic evaluation. We will introduce the AMCP PVI Payer council who will work to provide guidance on the methodology, payer needs and work with payer feedback.
Payers are invited to participate in the AMCP PVI Evidence & Value Innovation Program, an open initiative providing access to PVI assessments and AMCP eModels across 100+ therapies. Participants will have the opportunity to evaluate, apply, and provide feedback on this approach—helping shape the future of evidence and value assessment in managed care.
Featuring:
Allen Lising
Strategic Advisor
Digital Health Outcomes
Jeff Dunn, PharmD, MBA
Chief Clinical Officer,
Cooperative Benefits Group
Brought to you by Digital Health Outcomes
Wednesday, April 15 | 12-1:15pm | Invitation-Only
The Evolving Treatment Landscape of Hemophilia: Key Stakeholder Perspectives
Panel discussion on the current treatment landscape of hemophilia to understand the remaining unmet needs and challenges from a broad range of perspectives. The session will include an overview of hemophilia management, a discussion on the cost considerations and challenges in access to care, and an opportunity for collaboration and networking across industry stakeholders.
Sponsored by: Novo Nordisk
Wednesday, April 15 | 12:30-12:50pm | RWE Arena
The Real-World Impact of REMS and Black Box Warnings on Drug Monitoring
This research study explores the real-world impact of Risk Evaluation and Mitigation Strategies (REMS) and Black Box Warnings (BBW) on laboratory drug safety monitoring in a schizophrenia case study. This retrospective cohort study was conducted in the Healthcare Integrated Research Database (HIRD) and compares the rates of Absolute Neutrophil Count (ANC) monitoring in schizophrenia patients taking clozapine or olanzapine prior to and after removal of the Clozapine REMS program. 2,508 (86.1%) of 2,914 and 59 (77.6%) of 76 clozapine users had evidence of ANC monitoring before and after the clozapine REMS program was removed, respectively. 14,029 (52.4%) of 26794 and 359 (48.6%) of 739 olanzapine users had evidence of ANC monitoring before and after the clozapine REMS program was removed, respectively. ANC monitoring was more common in schizophrenia patients newly initiating clozapine compared to olanzapine before and after the removal of the clozapine REMS program. The proportion of patients receiving ANC monitoring decreased in both cohorts after the clozapine REMS program was removed.
Featuring:
Daniel Dudman, PharmD
Senior Researcher
Carelon Research
Brought to you by AMCP Research Institute
Wednesday, April 15 | 12:30-1pm | The Spotlight Stage
When testing falls short: The downstream clinical and economic impact of limited NGS in mCRC
Molecular testing strategies range from sequential single-gene approaches to next-generation sequencing (NGS) panels that allow broader and more efficient identification of actionable genomic alterations, transforming the management of metastatic colorectal cancer. We developed a cost-consequence framework to evaluate diagnostic testing costs, including biopsy-related procedures, as well as treatment-related costs and outcomes of large-panel NGS, small-panel NGS, and sequential single-gene testing (SGT). Large-panel NGS was associated with higher costs than small-panel NGS and lower costs than sequential SGT. In terms of clinical outcomes, Large-panel NGS was associated with higher life years gained compared with small-panel NGS and outcomes that were broadly comparable to sequential SGT.
Sponsored by: Merck
Wednesday, April 15 | 12:50-1:10pm | RWE Arena
Impact of Discordant Capecitabine and 5-Fluorouracil Label Warnings on Real-World DPYD Gene Testing
This research explores the potential impact of the discordant severity between capecitabine and 5-fluorouracil drug label warnings over time (i.e., since 2022) on the prevalence of DPYD gene testing before initiating treatment with either antineoplastic agent. A time-segmented, cross-sectional study of new users of capecitabine or 5-fluorouracil identified was conducted in the Healthcare Research Integrated Database (HIRD), a US administrative claims database.
The prevalence of pre-emptive DPYD gene testing in the 12-month baseline period before new use of either antineoplastic agent was estimated and compared between three distinct time periods: The first period ran from Dec 15, 2022 (one day after the FDA first approved an updated drug label warning for capecitabine but not 5-fluorouracil) to Mar 21, 2024 (when the FDA updated the 5-fluorouracil drug label warning to align with capecitabine); marking a strong vs weak non-boxed drug label warning comparison. The second period was a control period when both drugs had strong but non-boxed drug label warning i.e., from Mar 22, 2024, to Oct 3, 2025. The third period ran from Oct 4, 2025 (one day after the FDA updated the capecitabine, but not 5-fluorouracil, to a black box warning) to Oct 31, 2025. In each time segment, over 95% of observed new users initiated 5-fluorouracil. In the first period, the prevalence of DPYD gene testing was higher (2.1%) among capecitabine new users (i.e., strong drug label warning), compared to 5-fluorouracil new users (0.2%) with a weak drug label warning. In the second period where both groups had strong non-boxed drug label warnings, the prevalence of DPYD testing remained higher among new capecitabine users (5.2%) than new 5-fluorouracil users (0.5%). In the third period marked by capecitabine-only back box warning, 8.2% of new capecitabine users received DPYD gene testing, compared to 0.6% of new 5-fluorouracil users. These suggest a benefit, albeit limited, of strong warnings (e.g. black box warnings). Other approaches should be coupled with the recent update of 5-fluorouracil to its own black box warning, to optimize uptake of pre-emptive laboratory monitoring of DPYD.
Featuring:
Dami Onasanya, MD, MPH
Senior Researcher/Principal Investigator
Carelon Research
Brought to you by AMCP Research Institute
