TRULANCE® for Irritable Bowel Syndrome with Constipation in Adults is now Available to Canadians to Help Meet Treatment Gap that leaves 70 Per cent of Patients Unsatisfied

Bausch Health, Canada part of Bausch Health Companies Inc. (NYSE: BHC) (TSX: BHC), ("Bausch Health" or the "Company") today announced the availability through pharmacies across Canada of its new prescription treatment TRULANCE® (plecanatide).

TRULANCE(R) product package (CNW Group/Bausch Health)

TRULANCE is approved by Health Canada for the treatment of irritable bowel syndrome with constipation (IBS-C) in adults, 2 and is the first treatment brought to market in Canada by the gastrointestinal division of the Company. Canadian treatment guidelines for IBS-C recommend a variety of non-pharmaceutical and pharmaceutical approaches to treatment, 3 but 70 per cent of surveyed IBS-C patients report no treatment had thus far completely relieved their symptoms. 4

"Bausch Health, Canada is proud to launch TRULANCE as the first therapy brought to the Canadian market in an area where there is a great unmet need for Canadian patients and for a condition for which the prevalence in Canada is one of the highest in the world," said Ginette Gagné, interim president and general manager and vice president, Finance, Bausch Health , Canada . "We know doctors are seeking alternatives to improve care for those Canadians with the often-debilitating symptoms of IBS-C."

TRULANCE provides a solution to the treatment gap currently experienced by patients suffering from IBS-C.

In a recent survey of IBS-C patients across Canada , almost three out of four (72 per cent) said not all their symptoms are under control. Almost six out of 10 (57 per cent) said their symptoms prevent them from enjoying their daily activities and roughly the same number (56 per cent) feel their symptoms prevent them from reaching their full potential in life. 5 The seriousness and impact of IBS symptoms is reflected in a 2018 survey in which Canadians with IBS reported they would give up 25 per cent of their remaining life (15 years) to live a symptom-free life. 6

"Many people with IBS-C suffer in silence or with unsatisfactory treatments, because it is not a life-threatening acute disease, but it does have a big impact on their lives," said Dr. Louis Liu , chief, Division of Gastroenterology and Hepatology, University Health Network, Toronto . "It often affects people in early-to-middle age during the very busy and productive part of their lives, so it is important that it gets treated to the best extent possible, which is why having a new treatment option is very useful."

"We welcome a new treatment for IBS-C for Canadians, because we know current treatment options are not meeting the needs of every person with this condition," said Gail Attara , chief executive officer of the Gastrointestinal Society. "Our own large survey of persons living with IBS showed that only one in five felt confident their symptoms were under control. 7 This clearly demonstrates a dire need for new treatment options for those who are living with this invisible condition."

"With the prevalence of IBS being so high in Canada , we are thrilled to hear there is a new treatment option available to help Canadians manage the symptoms and severity of IBS-C," said Kelsey Cheyne , executive director of the Canadian Digestive Health Foundation. "This works towards our vision to help empower all Canadians to manage their digestive health with confidence and optimism."

About irritable bowel syndrome with constipation (IBS-C)
Irritable bowel syndrome (IBS) involves frequent and intense symptoms of abdominal cramping, bloating, constipation or diarrhea to the extent that they interfere with day-to-day living. 8 IBS-C is one of four subtypes of IBS, which occurs when the digestive system contracts slowly, delaying transit time for products of digestion, resulting in hard, difficult to pass, infrequent stools (constipation). The other forms are IBS-D (diarrhea) and IBS-M (mixed, both constipation and diarrhea symptoms) and IBS-U (unclassified). Constipation-predominant IBS represents about 30% of IBS cases. 9

IBS affects up to one in five Canadians at any given time 10 and Canada has one of the highest prevalences of the condition in the world. 11 The lifetime risk for a Canadian to develop IBS is 30%, with it affecting 20% of the population at any given time, and in Canada and most Western nations, IBS arises significantly more frequently in women than in men. 12 Two-thirds (67%) of Canadians with IBS-C say their symptoms make them feel self-conscious, and 60% say it is difficult for them to plan things, because they never know when their symptoms will act up; half (51%) say their symptoms cause them to stay home often. 13

About TRULANCE   ® (plecanatide tablets) in Canada
TRULANCE is a guanylate cyclase-C agonist, which mimics the effect of natural hormones in the body, giving it a unique method of action which allows it to act in the small intestine in a pH-sensitive manner to facilitate fluid secretion, increase intestinal transit, and decrease the activity of pain-sensitive nerves in the intestines. 14 In clinical studies, TRULANCE provided a statistically significant patient self-evaluated reduction in IBS disease severity and a statistically significant reduction in IBS symptoms versus placebo. 15 In the two clinical trials on which the approval of TRULANCE was based, 30.2 per cent and 21.5 per cent respectively of TRULANCE patients were considered overall responders, meaning they experienced both a significant decrease in abdominal pain and a significant increase in complete spontaneous bowel movements compared to those on placebo. 16 In clinical trials, the incidence of serious adverse events in patients using TRULANCE was low (0.8 per cent) and similar to that recorded in the placebo arm of the studies. 17 TRULANCE has not been studied in or approved for patients under the age of 18. 18

About the IBS-C patient survey 19
Statistics about the current attitudes and experiences of Canadians with IBS-C come from a comprehensive survey commissioned by Bausch Health, Canada in September and October 2021 and conducted by the research firm Callosum. The survey received data from 784 Canadians aged 18 and older who have been diagnosed with IBS-C specifically or have diagnosed with IBS generally but have symptoms of constipation. The average age of respondents was 47 years; 72% were females and 28% were males, reflecting the greater incidence of IBS-C among females. Respondents came from all regions of Canada in very close proportion to each region's respective share of the Canadian population.

About Bausch Health Companies Inc.
Bausch Health Companies Inc. (NYSE/TSX: BHC ) is a global company whose mission is to improve people's lives with our health care products. We develop, manufacture and market a range of pharmaceutical, medical device and over-the-counter products, primarily in the therapeutic areas of eye health, gastroenterology, and dermatology. We are delivering on our commitments as we build an innovative company dedicated to advancing global health. In Canada, the Company's prescription product portfolio is focused on eye health, dermatology, and cardio-metabolic conditions. More information can be found on the Company's website at bauschhealth.ca .


_____________________
REFERENCES


1.

Bausch Health, Canada, Understanding Patients' Perceptions and Treatment Habits of IBS-C , research report by
Callosum, October 2021, p. 15.


2.

Bausch Health, Canada, TRULANCE Product Monograph dated March 17, 2021, Indications, p. 4.


3.

Moayyedi P et al, Canadian Association of Gastroenterology Clinical Practice Guideline for the Management of
Irritable Bowel Syndrome (IBS), Journal of the Canadian Association of Gastroenterology , 2019, 2(1), 6–29.


4.

Bausch Health, Canada, Understanding Patients' Perceptions and Treatment Habits of IBS-C , research report by
Callosum, October 2021, p. 15.


5.

Bausch Health, Canada, Understanding Patients' Perceptions and Treatment Habits of IBS-C , research report by
Callosum, October 2021, p. 14.


6.

Canadian Digestive Health Foundation, Irritable Bowel Syndrome Statistics, https://cdhf.ca/digestive-
disorders/irritable-bowel-syndrome-ibs/statistics/
.


7.

Gastrointestinal Society. 2016 Survey Results Irritable Bowel Syndrome (IBS). https://badgut.org/ibs-survey-
results/
.


8.

Gastrointestinal Society, Irritable Bowel Syndrome (IBS), https://badgut.org/information-centre/a-z-digestive-
topics/ibs/
.


9.

Ibid.


10.

Ibid.


11.

Canadian Digestive Health Foundation, Irritable Bowel Syndrome Statistics, https://cdhf.ca/digestive-
disorders/irritable-bowel-syndrome-ibs/statistics/
.


12.

Gastrointestinal Society, Irritable Bowel Syndrome (IBS), https://badgut.org/information-centre/a-z-digestive-
topics/ibs/
.


13.

Bausch Health, Canada, Understanding Patients' Perceptions and Treatment Habits of IBS-C , research report by
Callosum, October 2021, p. 14.


14.

Bausch Health, Canada, TRULANCE Product Monograph dated March 17, 2021, Mechanism of Action, p. 11-12.


15.

Bausch Health, Canada, TRULANCE Product Monograph dated March 17, 2021, Clinical Trials, Patient Global
Rating (PGR) Assessments, p. 19


16.

Bausch Health, Canada, TRULANCE Product Monograph dated March 17, 2021, Study Results, p. 16.


17.

Bausch Health, Canada, TRULANCE Product Monograph dated March 17, 2021, Adverse Reactions Overview, p.
9


18.

Bausch Health, Canada, TRULANCE Product Monograph dated March 17, 2021, Pediatrics, p. 4.


19.

Bausch Health, Canada, Understanding Patients' Perceptions and Treatment Habits of IBS-C , research report by
Callosum, October 2021.


________________________

THE BURDEN FOR CANADIANS OF IRRITABLE BOWEL SYNDROME WITH CONSTIPATION (IBS-C) (CNW Group/Bausch Health)

SOURCE Bausch Health

Cision View original content to download multimedia: https://www.newswire.ca/en/releases/archive/February2022/08/c9054.html

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  • One-year clinical trial data for the next-generation, investigational, Sphere-360™ single-shot PFA catheter show impressive safety, performance, and efficiency results for paroxysmal Afib
  • Dual-energy (RF/PF), focal Sphere-9™ catheter demonstrates efficacy for linear ablation in persistent AFib
  • Medtronic continues legacy of leadership in innovation, showcasing arrhythmia management portfolio at Heart Rhythm Society annual meeting

Medtronic plc (NYSE: MDT), a global leader in healthcare technology, today announced positive clinical outcomes from two studies in atrial fibrillation (AFib) patients treated with the Affera™ family of technologies, including the next-generation Sphere-360™ single-shot pulsed field ablation (PFA) catheter and the groundbreaking Sphere-9™ combination mapping and dual-energy focal PFA catheter. Data were presented in High Impact Science Sessions at the Heart Rhythm Society 2025 Annual Meeting in San Diego ; the Sphere-360 study was simultaneously published in the Heart Rhythm Journal .

(PRNewsfoto/Medtronic plc)

Sphere-360 Study Safety and Performance

Sphere-360 is an investigational, first-of-its-kind, single-shot PFA mapping and ablation catheter for treatment of paroxysmal atrial fibrillation (PAF). Results for Sphere-360 at one year, in a prospective, single-arm, multi-center trial performed in European centers, demonstrated freedom from arrhythmia recurrence in 88% of patients, with chronically durable pulmonary vein isolation (PVI) in 98% of targeted veins and no reported safety events in a sub-group treated with the most optimized waveform. The Sphere-360 catheter has a large, conformable lattice design that can be modified into various shapes, is seamlessly integrated with the Affera Mapping and Ablation System and utilizes an 8.5 Fr sheath – the smallest in any single-shot PFA technology.

"The Affera technology is a sophisticated ecosystem, including an advanced, intuitive mapping system and catheters that are seamlessly integrated to offer treatment options for different cardiac arrhythmias. It is encouraging to see the promising results for Sphere-360, which can easily create circumferential lesions without the need for catheter rotation," said Vivek Reddy , M.D., Director of Cardiac Arrhythmia Services for the Mount Sinai Health System in New York City . "The study results showed Sphere-360 has a promising safety and performance profile with zero serious adverse events observed. Upon approval, Sphere-360 will be a valuable addition to Medtronic's Affera system, which has been a game changer for Afib treatment and physician workflow."

Medtronic intends to begin its U.S. pivotal trial for the Sphere-360 catheter later this calendar year. Worldwide, Sphere-360 is currently investigational and not approved for sale or distribution.

Sphere-9 for Linear Ablation

Additionally, in a sub-analysis from the Sphere Per-AF IDE study , results demonstrated that the Sphere-9 catheter can be used safely and effectively to create linear lesions in persistent AF patients. Linear ablation is often used in conjunction with PVI to improve the chances of restoring a normal heart rhythm without recurrence in persistent AF patients. The Sphere Per-AF IDE study evaluated the safety, efficacy and efficiency of Affera and Sphere-9 in persistent AF and led to the FDA approval of Affera in October 2024 .

"True to our Medtronic mission for patients and legacy of innovation, we are delivering our best-in-class technologies to physicians and improving care for AFib patients, and we are not slowing down," said Rebecca Seidel , president of the Cardiac Ablation Solutions business at Medtronic, which is part of the Cardiovascular portfolio. "These results signify another step forward and energize us as we continue to earn and build our leadership position in electrophysiology every day."

Medtronic is the only company with two PFA offerings for physicians and patients. The PulseSelect™ Pulsed Field Ablation System offers physicians a safe, single-shot solution for pulmonary vein isolation (PVI) and is now available in more than 30 countries. The Affera system together with the Sphere-9 catheter enables physician treatment flexibility with its wide area focal design and 9mm lattice tip that can used with an 8.5Fr sheath. Affera is available in Europe , Australia and New Zealand , with global expansion ongoing.

AFib is one of the most common and undertreated heart rhythm disorders, affecting more than 60 million people worldwide. 1 Afib is a progressive disease, often beginning as paroxysmal AFib (presents intermittently) and progressing to persistent (lasts for more than 7+ days without stopping). As the disease progresses, the risk of serious complications including heart failure, stroke and risk of death increases 2-5 .

For more information on the Affera PFA system and the Sphere-9 catheter, visit Medtronic.com.

About Medtronic

Bold thinking. Bolder actions. We are Medtronic. Medtronic plc, headquartered in Galway , Ireland , is the leading global healthcare technology company that boldly attacks the most challenging health problems facing humanity by searching out and finding solutions. Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people across more than 150 countries. Our technologies and therapies treat 70 health conditions and include cardiac devices, surgical robotics, insulin pumps, surgical tools, patient monitoring systems, and more. Powered by our diverse knowledge, insatiable curiosity, and desire to help all those who need it, we deliver innovative technologies that transform the lives of two people every second, every hour, every day. Expect more from us as we empower insight-driven care, experiences that put people first, and better outcomes for our world. In everything we do, we are engineering the extraordinary. For more information on Medtronic (NYSE: MDT), visit www.Medtronic.com and follow Medtronic on LinkedIn .

Any forward-looking statements are subject to risks and uncertainties such as those described in Medtronic's periodic reports on file with the Securities and Exchange Commission. Actual results may differ materially from anticipated results.

References

  1. Roth GA, Mensah GA, Johnson CO et al. Global Burden of Cardiovascular Diseases and Risk Factors, 1990-2019: Update From the GBD 2019 Study. J Am Coll Cardiol 2020;76:2982-3021.
  2. Miyasaka Y, Barnes ME, Bailey KR, et al. Mortality trends in patients diagnosed with first atrial fibrillation: a 21-year community-based study. J Am Coll Cardiol 2007;49:986-92.
  3. Hindricks G, Potpara T, Dagres N, et al. 2020 ESC Guidelines for the diagnosis and management of atrial fibrillation developed in collaboration with the European Association of Cardio-Thoracic Surgery (EACTS). Eur Heart J 2020.
  4. Wolf PA , Abbott RD, Kannel WB. Atrial fibrillation as an independent risk factor for stroke: the Framingham Study. Stroke 1991;22:983-8.
  5. Lubitz SA, Moser C, Sullivan L, et al. Atrial fibrillation patterns and risks of subsequent stroke, heart failure, or death in the community. J Am Heart Assoc 2013;2:e000126

Dr. Reddy is a paid consultant for Medtronic.

Contacts:
Leslie Williamson
Public Relations
+1-612-227-5099

Ryan Weispfenning
Investor Relations
+1-763-505-4626

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(PRNewsfoto/Medtronic plc)

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About the Diabetes Business at Medtronic ( www.medtronicdiabetes.com )
Medtronic Diabetes is on a mission to alleviate the burden of diabetes by empowering individuals to live life on their terms, with the most advanced diabetes technology and always-on support when and how they need it. We've pioneered first-of-its-kind innovations for over 40 years and are committed to designing the future of diabetes management through next-generation sensors (CGM), intelligent dosing systems, and the power of data science and AI while always putting the customer experience at the forefront.

About Medtronic
Bold thinking. Bolder actions. We are Medtronic. Medtronic plc, headquartered in Galway , Ireland , is the leading global healthcare technology company that boldly attacks the most challenging health problems facing humanity by searching out and finding solutions. Our Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people across more than 150 countries. Our technologies and therapies treat 70 health conditions and include cardiac devices, surgical robotics, insulin pumps, surgical tools, patient monitoring systems, and more. Powered by our diverse knowledge, insatiable curiosity, and desire to help all those who need it, we deliver innovative technologies that transform the lives of two people every second, every hour, every day. Expect more from us as we empower insight-driven care, experiences that put people first, and better outcomes for our world. In everything we do, we are engineering the extraordinary. For more information on Medtronic (NYSE: MDT), visit www.Medtronic.com and follow Medtronic on LinkedIn .

Any forward-looking statements, including, but not limited to, statements regarding the partnership between Medtronic and Abbott, strategic and other potential benefits of the partnership, Abbott's products and product candidates, and other statements about Medtronic managements' future expectations, beliefs, goals, plans or prospects, are subject to risks and uncertainties including, but not limited to, the ability to obtain regulatory approvals, and other risks and uncertainties such as those described in Medtronic's reports and other filings with the Securities and Exchange Commission. Actual results may differ materially from anticipated results. Medtronic cautions investors not to place considerable reliance on the forward-looking statements contained in this press release. These forward-looking statements speak only as of the date of this document, and Medtronic undertakes no obligation to update or revise any of these statements except to the extent required by law.

Contacts:
Janet Cho
Public Relations
+1-818-403-7028

Ryan Weispfenning
Investor Relations
+1-763-505-4626

Cision View original content to download multimedia: https://www.prnewswire.com/news-releases/medtronic-advances-abbott-cgm-partnership-with-fda-submission-of-interoperable-insulin-pump-302437337.html

SOURCE Medtronic plc

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