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Vertex makes headway in UK reimbursement | BioPharma Dive

Dive Brief: - Scotland health authorities have agreed to reimburse the two newest cystic fibrosis drugs from Vertex Pharmaceuticals, opening the door to therapy for roughly 400 eligible patients. - The decision is a victory for Vertex, as the company faces tro

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Dive Brief:

  • Scotland health authorities have agreed to reimburse the two newest cystic fibrosis drugs from Vertex Pharmaceuticals, opening the door to therapy for roughly 400 eligible patients.
  • The decision is a victory for Vertex, as the company faces trouble securing reimbursement in the broader U.K. market. The agency that recommends whether drugs get covered in the U.K. has taken issue with the price of Vertex's products — and though both parties claim to have revised their proposals to create a more middle-ground resolution, they have yet to come to an agreement.
  • Vertex's deal with Scotland provides five years of coverage for Orkambi and Symkevi while also requiring the company to collect real-world data on the drugs, which "will support any future submissions to the Scottish Medicines Consortium," according to a Thursday statement.

Dive Insight:

With more than 10,000 registered patients, the U.K. has one of the largest cystic fibrosis populations in the world. It's a patient base and market Vertex wants to break into, but reimbursement remains a barrier.

A contentious debate between Vertex and the U.K.'s National Institute for Health and Care Excellence, or NICE, has gone on for more than a year. While mostly focused on Orkambi (lumacaftor/ivacaftor), the back and forth has also extended to Symkevi (tezacaftor/ivacaftor and ivacaftor) and another Vertex drug likely to gain approval next year.

At the heart of the debates is cost. By 2018, the respective list prices for Orkambi and Symkevi, which is marketed as Symdeko in the U.S., were around $273,000 and $292,000.

NICE sees those prices as too high, and it isn't alone. Last May, an influential cost watchdog called ICER concluded the list prices of Orkambi, Symdeko and Vertex's other marketed drug Kalydeco (ivacaftor) would have to come down more than 70% to meet common cost-effectiveness thresholds.

"NICE has been clear that Vertex's pricing is unsupportable," wrote National Health Service, the U.K. health agency that oversees NICE, in a letter last July that followed a meeting with the company. "If Vertex really believe they are offering a reasonable deal they should waive their confidentiality clause and let patients and taxpayers judge whether it is fair."

NHS is the healthcare system for the entire U.K., but agencies in areas like Scotland and Wales can make reimbursement decisions at a regional level. The system allows for deals like the one just inked between Vertex and the Scottish Medicines Consortium.

While Scotland won't bring a "material revenue stream" to Vertex's cystic fibrosis business, it could bode well for the ongoing negotiations with NICE and NHS, according to RBC analyst Brian Abrahams.

"[G]iven the proximity of Scotland, it is possible that this agreement could increase public and political pressures on England to move forward with obtaining access to [Vertex] medicines, which is a more meaningful population in terms of potential revenue contribution," Abrahams wrote in a Sept. 12 note to clients.

Investors might not yet be sold on that line of thinking. Vertex shares were unfazed by the agreement, trading less than 1% down Thursday morning.

Jefferies analyst Michael Yee views the Scotland market as a roughly $100 million revenue opportunity for Vertex, assuming there are 900 cystic fibrosis patients who each come in at a $125,000 price point.

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Helpful context for this guide

Source-derived material selected through this article’s indexed topics.

Related questions

01How Do I Know if Alyftrek Is Working?

Your health care provider will monitor your progress while you are taking Alyftrek to make sure the treatment is effective. One key test used to measure progress is lung function testing (like FEV₁%), which checks how well your lungs are working. If Alyftrek is working, your FEV₁% may get better or remain the same over time. Another important measure is sweat chloride levels. Higher sweat chloride levels are a sign of cystic fibrosis, and Alyftrek may help lower these levels by helping the CFTR protein work better. Your health care provider may order sweat chloride tests to track improvements. In addition to lab tests, you may notice fewer lung infections, better breathing, less coughing, and increased energy levels. Your health care provider will also monitor for any side effects and may adjust your treatment plan if needed. Always follow up with your health care team to discuss any changes in symptoms or concerns about your treatment. Do not stop taking Alyftrek without talking to your health care provider first. Your symptoms may get worse again if you stop or change any of your medicines.

Source: www.webmd.com ↗
02What is cystic fibrosis? A Mayo Clinic expert explains

Learn more from pulmonologist Sarah Chalmers, M.D. Cystic fibrosis (CF) is a condition passed down in families that causes damage to the lungs, digestive system and other organs in the body. CF affects the cells that make mucus, sweat and digestive juices. These fluids, also called secretions, are usually thin and slippery to protect the body's internal tubes and ducts and make them smooth pathways. But in people with CF, a changed gene causes the secretions to become sticky and thick. The secretions plug up pathways, especially in the lungs and pancreas. CF gets worse over time and needs daily care, but people with CF usually can attend school and work. They often have a better quality of life than people with CF had in past decades. Better screening and treatments mean that people with CF now may live into their mid- to late 50s or longer, and some are being diagnosed later in life.

Source: www.mayoclinic.org ↗
03What Are the Symptoms of Cystic Fibrosis?

The symptoms of cystic fibrosis vary. Some children will have symptoms at birth, while others may not have symptoms for weeks, months, or even years. The severity of symptoms also varies, with some children showing only mild digestive and lung problems and others having severe food-absorption problems and life-threatening breathing complications. The most common symptoms of cystic fibrosis are: Salty-tasting skin , which parents notice when they kiss their child Frequent coughing , wheezing , or bouts of pneumonia or sinusitis Difficulty breathing that keeps getting worse Big appetite but poor weight gain Bulky, smelly, greasy bowel movements Over time, the symptoms of cystic fibrosis can worsen and may include: Chronic productive cough, recurrent lung infections Obstructive lung disease ( emphysema ) Chronic nasal congestion and sinus infections Pancreatitis , a painful inflammation of the pancreas Liver disease Diabetes Gallstones

Source: www.webmd.com ↗
04What to expect from your doctor

After getting detailed information about the symptoms and your family's medical history, your healthcare professional may order tests to help with diagnosis and plan treatment. Your healthcare professional also may ask questions, such as: What symptoms are you or your child having? When did the symptoms start? Does anything make the symptoms better or worse? Has anyone in your family ever had cystic fibrosis? Has growth been average and weight been stable? Cystic fibrosis. National Heart, Lung, and Blood Institute. https://www.nhlbi.nih.gov/health/cystic-fibrosis. Accessed Aug. 8, 2024. Bronchiectasis. National Heart, Lung, and Blood Institute. https://www.nhlbi.nih.gov/health/bronchiectasis. Accessed Aug. 8, 2024. FAQs: Cystic fibrosis: Prenatal screening and diagnosis. American College of Obstetricians and Gynecologists. https://www.acog.org/womens-health/faqs/cystic-fibrosis-prenatal-screening-and-diagnosis. Accessed Aug. 8, 2024. Ferri FF. Cystic fibrosis. In: Ferri's Clinical Advisor 2025. Elsevier; 2025. https://www.clinicalkey.com. Accessed Aug. 8, 2024. Kliegman RM, et al., eds. Cystic fibrosis. In: Nelson Textbook of Pediatrics. 22nd ed. Elsevier; 2025. https://www.clinicalkey.com. Accessed Aug. 8, 2024. Kellerman RD, et al. Cystic fibrosis. In: Conn's Current Therapy 2024. Elsevier; 2024. https://www.clinicalkey.com. Accessed Aug. 8, 2024. Lockwood CJ, et al., eds. Respiratory diseases in pregnancy. In: Creasy and Resnik's Maternal-Fetal Medicine: Principles and Practice. 9th ed. Elsevier; 2023. https://www.clinicalkey.com. Accessed Aug. 8, 2024. Ong T, et al. Cystic fibrosis: A review. JAMA. 2023; doi:10.1001/jama.2023.8120. Rubin R. Tackling the misconception that cystic fibrosis is a "white people's disease." JAMA. 2021; doi:10.1001/jama.2021.5086. Care centers. Cystic Fibrosis Foundation. https://www.cff.org/managing-cf/care-centers. Accessed Aug. 8, 2024. Trikafta (prescribing information). Vertex Pharmaceuticals Inc.; 2023. https://www.trikafta.com/. Accessed Aug. 8, 2024. Symdeko (prescribing information). Vertex Pharmaceuticals Inc.; 2023. https://www.symdeko.com/. Accessed Aug. 8, 2024. Orkambi (prescribing information). Vertex Pharmaceuticals Inc.; 2023. https://www.orkambi.com/. Accessed Aug. 8, 2024. Kalydeco (prescribing information). Vertex Pharmaceuticals Inc.; 2023. https://www.kalydeco.com/. Accessed Aug. 8, 2024. Pilewski JM. Update on lung transplantation for cystic fibrosis. Clinics in Chest Medicine. 2022; doi:10.1016/j.ccm.2022.07.002. Fridell JA, et al. Pancreas transplantation for cystic fibrosis: A frequently missed opportunity. Clinical Transplantation. 2021; doi:10.1111/ctr.14371. Wadsworth LE, et al. Non-invasive ventilation is associated with long-term improvements in lung function and gas exchange in cystic fibrosis adults with hypercapnic respiratory failure. Journal of Cystic Fibrosis. 2021; doi:10.1016/j.jcf.2021.05.011. Allscripts EPSi. Mayo Clinic. Medical review (expert opinion). Mayo Clinic. Oct. 18, 2024.

Source: www.mayoclinic.org ↗
05Why do I need a sweat test?

A sweat test may be ordered if your health care provider suspects you or your child has cystic fibrosis (CF). It's most commonly ordered for newborns. In the United States, babies have newborn screening  tests to check for a variety of conditions, including CF. If a screening test shows that your baby may have CF, a sweat test will be needed to make a diagnosis.

Source: medlineplus.gov ↗
Research context

Read sources and limitations before applying a claim.

Research and Statistics: Who Has Cystic Fibrosis?

About 40,000 people are living with cystic fibrosis in the United States, and there are approximately 105,000 people with CF worldwide. (3) More than 75 percent of people with the disease are diagnosed by age 2, and more than half of all people living with cystic fibrosis are 18 or older. CF occurs predominantly in white populations, at a rate of 1 in 2,500 births. Between 2 and 5 percent of white people are carriers of the CFTR gene variant but have no overt clinical signs of disease. The disease is less common among African Americans, occurring at the much lower frequency of approximately 1 out of 17,000 births. (15) CF gene variants are most prevalent in persons of northern and central European ancestries or of Ashkenazi Jewish descent. They are rarely found in Native Americans, Asians, or native Africans. (16) CF is equally common among men and women, but women patients fare significantly worse than male patients with the disease. The median survival age for female CF patients is about three years younger than it is for men, but the reasons for the poorer survival rates among women are not completely understood. (17)

Source: everydayhealth.com ↗
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Peptide Therapy Guide Editorial Team

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