Hepatology Center of Excellence
Orsini’s Hepatology Center of Excellence launched in 2024 with our first program for primary biliary cholangitis (PBC). Our dedicated Therapy Care Teams work with the physician’s office and insurance on a patient’s behalf so that our patients and their family have more time to focus on their treatment and quality of life. We are here to listen, provide counseling on treatment, including side-effect management, and assist with sourcing third-party financial assistance.
Benefits
Receive personalized support from a dedicated Therapy Care Team, including a primary pharmacy contact, clinical education, side-effects management, and scheduled refill calls.
Experience compassionate care that prioritizes patients and their families. Our team supports patients of all ages, from infants to the elderly, extending care to the entire care team.
Secure treatment coverage with assistance navigating payer and plan requirements. Our team proactively works with prescribers to obtain prior authorization and support appeals.
Ensure medication and essential medical supplies arrive when and where patients need them through coordination across prescribers, patients, and care teams to arrange free overnight shipping.
Minimize financial exposure through financial assistance programs. We successfully identify and assist in enrolling patients into manufacturer co-pay and foundation support programs.
Gain continuous access to a pharmacist, 24/7/365, ensuring ongoing care and clinical support for patients and prescribers to achieve better outcomes.
Support
Explore the rare hepatology conditions Orsini supports below or see All Hepatology Therapies available through Orsini.
A co-infection in individuals who have hepatitis B, HDV is the most severe form of viral hepatitis and affects approximately 40,000 people in the U.S. Those living with HDV often experience faster progression to liver fibrosis, cirrhosis and hepatic decompensation, and they have a higher risk of liver cancer and death.
| Full Name | Hepcludex® (bulevirtide‑gmod) |
| Drug | bulevirtide |
| Manufacturer | Gilead Sciences, Inc. |
| Route of Administration | Subcutaneous |
| Site of Care | Home |
| Approved Indication | The treatment of chronic hepatitis delta (HDV) infection in adults without cirrhosis or with compensated cirrhosis |
| Disease | Chronic hepatitis delta (HDV) infection |
| Therapeutic Area | Hepatology |
| Phone Number | 847-457-4259 |
| Fax Number | 877-860-2504 |
| Enrollment Form Link | Enrollment Form |
| Product Website | hepcludexhcp.com |
PBC is a rare, chronic disease that impairs liver function; bile flow is reduced, and bile acids accumulate in the liver, elevating liver enzyme numbers to dangerous levels. The disease affects about one in 1,000 women over the age of 40 and is associated with fatigue, itching, poor appetite, weight loss and an increased risk of liver-related death.
| Full Name | Livdelzi® (seladelpar) |
| Drug | Livdelzi |
| Manufacturer | Gilead Sciences, Inc. |
| Route of Administration | Oral |
| Site of Care | Home |
| Approved Indication | Treatment of primary biliary cholangitis (PBC) in combination with ursodeoxycholic acid (UDCA) in adults who have an inadequate response to UDCA, or as monotherapy in patients unable to tolerate UDCA |
| Disease | Primary Biliary Cholangitis (PBC) |
| Therapeutic Area | Hepatology |
| Enrollment Form Link | Enrollment Form |
| Phone Number | 888-263-8004 |
| Fax Number | 877-846-0402 |
| Product Website | livdelzihcp.com |
| Patient Resources | • PBCers Organization • Orsini/PBCers 2025 Webinar – "Specialty Pharmacy: Partners in Your Care" | Watch On-Demand → |
The Alex Rezcalla Foundation advances the development of therapies for individuals with Duchenne muscular dystrophy (DMD) through advocacy and research funding. It raises awareness of the DMD experience by hosting events, engaging the public, and building networks of support.
Learn more at alexrezkallafoundation.org
The Amyloidosis Research improves the lives of patients with amyloidosis and accelerates cutting edge research through collaborative, groundbreaking initiatives. ARC provides support, information, and resources to patients and caregivers, empowering them to access the best care possible.
Learn more at aci.org
Cure SMA is dedicated to finding treatments and a cure for spinal muscular atrophy (SMA) by funding research and supporting families. Since 1984, Cure SMA has grown to be the largest U.S.-based network of individuals, families, clinicians, and research scientists working together to advance SMA research, support individuals and families impacted by SMA, and educate public and professional communities about SMA.
Learn more at www.curesma.org
The US Hereditary Angioedema Association (HAEA) is a 501 (c)(3) non-profit advocacy and research organization serving people living with the rare genetic condition, Hereditary Angioedema (HAE), and their families. Founded and staffed by people with HAE and caregivers, the US HAEA is committed to actively engaging our community in a wide variety of grassroots activities that promote HAE education and awareness.
Learn more at haea.org
The HypoPARAthyroidism Association is a non-profit patient association working to improve the lives of people impacted by hypoPARAthyroidism through education, support, research, and advocacy. They raise awareness of hypoPARAthyroidism and bring change to the lives of those affected.
Learn more at hypopara.org
Jett Foundation empowers people and families impacted by Duchenne muscular dystrophy through the development of transformative programming, educational opportunities, and ongoing support for every stage of a Duchenne journey.
Learn more at jettfoundation.org
Muscular Dystrophy Association (MDA) is the #1 voluntary health organization in the United States for people living with muscular dystrophy, ALS, and over 300 other neuromuscular conditions. For 75 years, MDA has led the way in accelerating research, advancing care, and advocating support and inclusion of families living with neuromuscular disease.
Learn more at mda.org
The National MPS Society is committed to making a difference in the lives of MPS families through support, research, education, and advocacy. Families from around the world gain a better understanding of these rare genetically determined diseases through the Society’s assistance in linking them with healthcare professionals, researchers, and, perhaps most importantly, each other.
Learn more at mpssociety.org
The National Niemann-Pick Disease Foundation, Inc. (NNPDF) is a non-profit, patient advocacy and family support organization dedicated to supporting and empowering patients and families affected by Niemann-Pick disease, through education, collaboration and research. Founded in 1993, NNPDF serves families throughout the nation at all stages of their Niemann-Pick journey.
Learn more at nnpdf.org
The National PKU Alliance (NPKUA) works to improves the lives of individuals with PKU, pursue a cure by expanding research, and provide education and support to individuals living with PKU and their caregivers. Since its inception in 2008, NPKUA has supported numerous successful fundraising events, conferences, and internal support programs and has remained steadfast in its support of research endeavors.
Learn more at npkua.org
Parent Project Muscular Dystrophy (PPMD) is the largest nonprofit organization in the United States focused entirely on Duchenne muscular dystrophy. They take a comprehensive approach in the fight against Duchenne—funding research, raising awareness, promoting advocacy, connecting the community, and broadening treatment options.
Learn more at parentprojectmd.org
The Pompe Alliance is a Public Services Organization dedicated to the ideas of support, empowerment, and progress. It seeks to provide supportive services and information to patients, caregivers, medical professionals, and community stakeholders through a number of initiatives: financial assistance, advocacy, education, mentoring, and research recruitment
Learn more at pompealliance.com
The mission of the Pulmonary Fibrosis Foundation is to accelerate the development of new treatments and ultimately a cure for pulmonary fibrosis. Until this goal is achieved, the PFF is committed to advancing improved care of patients with PF and providing unequaled support and education resources for patients, caregivers, family members, and health care providers.
Learn more at pulmonaryfibrosis.org
The United Pompe Foundation was formed to assist patients and/or their families with medical costs and other expenses that these patents and families face and may not be able to cover, or fully cover, through their insurance.
Learn more at unitedpompe.com