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Sionna cystic fibrosis drug fails key trial, removing threat to Vertex | BioPharma Dive

Dive Brief: - An experimental cystic fibrosis drug from Sionna Therapeutics missed its main goal in a Phase 2 clinical trial, failing to show additive effects when layered on top of Vertex Pharmaceuticals’ popular medicine Trikafta, the company said Monday. -

Written by Peptide Therapy Guide Editorial Team
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This guide cannot diagnose a condition or recommend a personal treatment plan. Discuss medical questions with a qualified professional.

Dive Brief:

  • An experimental cystic fibrosis drug from Sionna Therapeutics missed its main goal in a Phase 2 clinical trial, failing to show additive effects when layered on top of Vertex Pharmaceuticals’ popular medicine Trikafta, the company said Monday.
  • The closely watched trial compared a combination of Sionna’s SION-719 and Trikafta to Trikafta alone and evaluated their relative impact on “sweat chloride levels,” a sign of a drug’s potential effect on the disease. The regimen didn’t yield a statistically significant, placebo-adjusted change on that measure, badly missing a mark set by Sionna leadership.
  • Sionna’s shares fell nearly 92% in early trading Monday, leaving the company worth less than the $268 million in available cash and equivalents it had as of June 30. Company executives said they intend “to take actions to preserve capital while evaluating next steps.” Vertex shares, meanwhile, climbed by 7%.

Dive Insight:

Sionna is one of many companies that have faltered in challenging Vertex’s main business, a multi-drug franchise projected to bring in $13 billion in revenue this year. Like others before it, Sionna’s goal has been to improve upon Vertex’s pioneering therapies, which modulate a key protein that’s defective in cystic fibrosis and have proven to slow disease progression.

Sionna raised hundreds of millions of dollars in private and public funding to support the effort, amassing a portfolio of drugs designed to stabilize a particularly tricky region of that defective protein, “CFTR.” It licensed some prospects from AbbVie, too, hoping to develop its own combination regimens.

Sionna has claimed its drugs could help normalize function of the CFTR protein in ways Vertex’s medicines don’t. The Phase 2 trial reported Monday was a key test of that theory. It was testing whether Trikafta and a drug code-named SION-719 could help lower sweat chloride levels more effectively than Trikafta alone.

Going into the trial, Sionna executives had suggested that an improvement of “10 millimoles per liter” of sweat would be “clinically meaningful” and differentiate its drug. Sionna instead said Monday that that number was just 1 millimole per liter, a difference that wasn’t statistically significant.

In a client note following the company’s announcement, Stifel analyst Paul Matteis said the data are “hard to explain [and] leaves us puzzled.”

Others, like RBC Capital Markets’ Brian Abrahams, were skeptical beforehand. In a Monday note, Abrahams wrote that the “unfavorable setup” of Sionna having a high valuation going into the readout “played out,” and that all expectations have now been “washed out” of the company’s stock.

Sionna’s path forward will now depend on other medications, among them the drugs it acquired from AbbVie. In its announcement Monday, Sionna reported positive data from a Phase 1 trial testing one of those AbbVie drugs in combination with a therapy Sionna developed.

In a separate note on Vertex, Abrahams called the Sionna news a “clearing event” that makes him much more confident in recommending that investors buy shares.

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Related questions

01What you can do

You might want to take a friend or family member with you to the appointment to help you remember information. Before your appointment, make a list of: Symptoms and when they started. Include anything that makes symptoms worse or better. All medicines, vitamins, herbs and supplements that you or your child take. Include the doses. Family history, such as whether anyone in your family has cystic fibrosis. Treatment you or your child have had for CF, if any. Include what the treatment was and if it helped. Any other medical conditions and their treatments. Questions to ask your healthcare professional. Questions to ask may include: What is likely causing these symptoms? What kinds of tests are needed? What treatment do you recommend? I or my child have other health conditions. How will cystic fibrosis affect them? Are there any limits needed? Feel free to ask other questions during your appointment.

Source: www.mayoclinic.org ↗
02Who Was Included in These Studies?

Overall, Alyftrek for cystic fibrosis treatment has been studied in a variety of people. Adults Adolescents Males and females Asian, Black, and White people

Source: www.webmd.com ↗
03Why 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 ↗
04What 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 ↗
05What 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 ↗
Research context

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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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