logo
Boehringer Ingelheim Launches Fast-acting Stroke Medication in the UAE, Reducing Treatment Administration to Five Seconds

Boehringer Ingelheim Launches Fast-acting Stroke Medication in the UAE, Reducing Treatment Administration to Five Seconds

Mid East Info28-02-2025

The newly approved treatment provides a fast-acting option for acute ischemic stroke (AIS) care.
Administered as a single IV bolus over a period of five to ten seconds, the treatment offers a significant improvement over regular one-hour-long treatments.
Dubai, United Arab Emirates – February 2025: Boehringer Ingelheim, a leading research-driven biopharmaceutical company, has launched a new acute ischemic stroke (AIS) medication with active ingredient Tenecteplase 25mg to enhance emergency stroke treatment in the UAE, offering a faster and more effective treatment option for emergency stroke care.
Launched in the UAE for the first time across the India, Middle East, Turkey and Africa region, the new medication can be delivered over five to ten seconds, compared to the previous treatments requiring a one-hour administration process. This simplified and rapid approach facilitates faster treatment administration in emergency settings, reducing both door-to-needle (DTN) times and door-in-door-out (DIDO) times. This can improve patient recovery outcomes and minimize long-term neurological deficits associated with stroke [i] .
Stroke is the second leading cause of death globally and a major contributor to disability, thereby imposing significant burdens on both patients and the economy [ii] . Many survivors face long-term disabilities, with up to 50% being chronically disabled [iii] . In the UAE, between 8,000 to 10,000 individuals suffer from a stroke each year, which amounts to one case every hour [iv] . Ischemic strokes occur when there is a blockage in a blood vessel, resulting in reduced blood supply to the brain [v] . Early recognition of symptoms is crucial for effective treatment. Common signs include sudden numbness or weakness, especially on one side of the body; confusion or trouble speaking; difficulty seeing in one or both eyes; dizziness or loss of balance; and a severe headache with no known cause [vi] .
The new medication was launched on 22 February during the 5th Dubai Neurology Congress, which brought together over 120 healthcare professionals from the UAE. Dr. Suhail Al Rukn, President of the Emirates Neurology Society and Consultant Neurologist highlighted the importance of time efficiency in stroke care. 'Time is brain,' Dr. Al Rukn said. 'Reducing the time between symptoms onset and treatment is crucial in saving lives and preserving brain function [vii] . For every minute that treatment is delayed, millions of brain cells are lost [viii] . Seeking immediate medical care can therefore greatly improve outcomes and minimize the risk of long-term disability. This new treatment offers a major leap forward by minimizing delays and simplifying the administration process, providing an opportunity to improve outcomes for stroke patients in the UAE.'
Ousama Alhaj, General Manager and Head of Human Pharma, Boehringer Ingelheim in the Near East and UAE added: 'The UAE, like many other countries around the world, faces a growing incidence of stroke cases each year [ix] , making timely treatment a priority. This new medication not only improves the efficiency of care delivery but also enhances the overall healthcare journey for patients. At Boehringer Ingelheim, we are committed to developing patient-centered health solutions that improve survival rates and long-term outcomes for stroke patients. We also remain committed to working closely with healthcare stakeholders to ensure these medications are accessible to those who need them.'
Administered at a dose of 0.25mg/kg (up to a maximum of 25mg) as a single intravenous bolus, the new treatment is now available in the UAE and underscores Boehringer Ingelheim's ongoing dedication to patient-centered innovation in healthcare, with a focus on early detection, prevention, and treatment. The company continues to strengthen its presence in the UAE by providing advanced medical solutions that address the needs of healthcare professionals and patients alike.
About Boehringer Ingelheim:
Boehringer Ingelheim is working on breakthrough therapies that improve the lives of humans and animals. As a leading research-driven biopharmaceutical company, the company creates value through innovation in areas of high unmet medical need. Founded in 1885 and family-owned ever since, Boehringer Ingelheim takes a long-term perspective. Around 52,000 employees serve more than 130 markets in the three business areas, Human Pharma, Animal Health, and Biopharmaceutical Contract Manufacturing.

Orange background

Try Our AI Features

Explore what Daily8 AI can do for you:

Comments

No comments yet...

Related Articles

Boehringer Ingelheim reaches more patients in 2024 and prepares new medicine launches - Middle East Business News and Information
Boehringer Ingelheim reaches more patients in 2024 and prepares new medicine launches - Middle East Business News and Information

Mid East Info

time22-04-2025

  • Mid East Info

Boehringer Ingelheim reaches more patients in 2024 and prepares new medicine launches - Middle East Business News and Information

Number of patients reached in 2024 jumps 8% to 66 million. In 2024, Boehringer Ingelheim in India, Middle East, Turkey and Africa (IMETA) region achieved net sales of EUR 855 million, reflecting a 17% increase compared to the previous year. R&D investments rise to EUR 6.2 billion, 23.2% of group net sales. Company prepares new product launches starting in 2025. Dubai, United Arab Emirates: Boehringer Ingelheim today announced a continued rise in the number of patients it reached, 66 million in 2024, up 8.0% from the previous year. Development of its current product pipeline is well on track, as the company prepares multiple new product launches, starting in 2025. Research & Development (R&D) investments rose to EUR 6.2 billion, or 23.2% of group net sales. Group net sales rose by 6.1%* to EUR 26.8 billion. 'As our current pipeline continues to mature and more products come closer to a potential market introduction, we have entered a pivotal phase of high investments, to bring these new innovations to patients,' said Hubertus von Baumbach, Chairman of the Board of Managing Directors. 'It is important that we use every opportunity to bring these new treatments to patients as fast as possible – this is our number one priority.' Strong Growth in IMETA: In India, Middle East, Turkey, and Africa (IMETA) region, the company recorded net sales of 855 million EUR (2023: 732 million EUR), a 17% increase compared to the previous year. Derek O'Leary, Regional Managing Director at Boehringer Ingelheim India, Middle East, Turkey and Africa (IMETA) said: 'Our strong performance in 2024 underscores our commitment to addressing unmet medical needs in both human and animal health. We will continue to work towards expanding access to innovative treatments for people and strengthen our efforts to safeguard animal health and well-being, impacting a greater number of lives. In partnerhip with our stakeholders, we are eager to build on this momentum in 2025 through further science-backed innovations tailored to the needs of both patients and animals.' Human Pharma: investing in existing products and new launches Human Pharma sales rose by 7.0%* to EUR 21.9 billion, led by the treatment of chronic kidney diseases, type 2 diabetes and heart failure, rose 14.6%* to EUR 8.4 billion. Treatments used for idiopathic pulmonary fibrosis and certain fibrosing interstitial lung diseases, grew 8.9%* to EUR 3.8 billion. The Human Pharma pipeline includes over ten new Phase II and III trials over the next 12 to 18 months, which will potentially result in a range of significant launches in the next five years. Human Pharma R&D spending rose to EUR 5.7 billion, or 27.6% of the business unit's net sales. 'If we look at the past five years, Boehringer Ingelheim has invested approximately EUR 25 billion in R&D,' said Frank Hübler, Member of the Board of Managing Directors with responsibility for Finance. 'With the innovations currently in our pipeline we will further increase investments in R&D in the years to come.' After positive data from pivotal studies, the company is preparing multiple new product launches to advance care for patients with Idiopathic Pulmonary Fibrosis and Progressive Pulmonary Fibrosis as well as the first orally administered, targeted therapy for previously treated HER2-mutated lung cancer patients. Both treatments have been submitted to regulatory authorities globally and first launches in the US are anticipated in the second half of this year, pending approval. Animal Health: rapid response against transboundary animal diseases Animal Health sales rose 1.9%* to EUR 4.7 billion in 2024, mainly driven by Pet Parasiticides and Therapeutics, Poultry and Ruminant. The parasiticides continued to strengthen its position as the top-selling brand in the industry, growing 14.0%* to EUR 1.4 billion. Last year, Boehringer Ingelheim supported livestock producers and governments by quickly providing vaccines and technical assistance for outbreaks of transboundary animal diseases (TADs), such as avian influenza, bluetongue virus and foot-and-mouth disease. These diseases pose a significant risk to animal health, impede global trade, and constrain food supply. Sustainable Development: Boehringer Ingelheim is on track in its target to become carbon neutral in its company operations by 2030. It increased global renewable electricity purchases to around 75% in 2024, primarily due to transitioning to renewable solutions at various sites, including Japan and China. A new biomass power plant was also commissioned at its Ingelheim site in Germany to boost on-site renewable energy generation to 95% of its energy needs. As part of its global effort to stop rabies, the company provided 46 million rabies vaccine doses and supported vaccination campaigns in endemic countries. The 'Angels' initiative, which aims to optimize the quality of treatment in existing stroke centers, added over 1,000 organizations to the network. It is the largest stroke community in the world, now encompassing 237,000 healthcare professionals from more than 9,000 hospitals in 158 countries and has helped 19 million stroke patients to date. Outlook: The general trends and developments of the past year are expected to continue to impact 2025. The company expects a continued rise in the number of patients reached, and a slight year-on-year increase in net sales, adjusted for currency and extraordinary effects. * sales growth numbers are adjusted for currency effects **one-sided p-value from a z-test of the null hypothesis ORR ≤30% Boehringer Ingelheim: Boehringer Ingelheim is a biopharmaceutical company active in both human and animal health. As one of the industry's top investors in research and development, the company focuses on developing innovative therapies that can improve and extend lives in areas of high unmet medical need. Independent since its foundation in 1885, Boehringer takes a long-term perspective, embedding sustainability along the entire value chain. Approximately 54,500 employees serve over 130 markets to build a healthier and more sustainable tomorrow.

Boehringer's nerandomilast meets primary endpoint in Phase III study FIBRONEER™-ILD, in progressive pulmonary fibrosis
Boehringer's nerandomilast meets primary endpoint in Phase III study FIBRONEER™-ILD, in progressive pulmonary fibrosis

Mid East Info

time12-03-2025

  • Mid East Info

Boehringer's nerandomilast meets primary endpoint in Phase III study FIBRONEER™-ILD, in progressive pulmonary fibrosis

Topline data from FIBRONEER™-ILD show that the investigational compound nerandomilast met its primary endpoint, which was the absolute change from baseline in forced vital capacity [mL] at week 52 versus placebo The FIBRONEER™-ILD trial is the second Phase III trial in which the investigational compound nerandomilast has met its primary endpoint [1] Initial safety and tolerability results of the FIBRONEER™-trials are generally consistent with the Phase II results in IPF; full efficacy and safety data from FIBRONEER™-ILD will be shared in the second quarter of 2025 Boehringer Ingelheim will submit a new drug application for nerandomilast for the treatment of PPF to the US Food & Drug Administration (FDA) and other health authorities worldwide Boehringer Ingelheim announced today that the FIBRONEER™-ILD trial met its primary endpoint, which was the absolute change from baseline in forced vital capacity (FVC) [mL] at week 52 versus placebo. FVC is a measure of lung function. [2] Initial data readouts of the FIBRONEER™-trials support a generally consistent safety and tolerability profile when compared to the Phase II idiopathic pulmonary fibrosis (IPF) study, with overall adverse events comparable to those seen in the placebo group. 3 Nerandomilast is an investigational oral, preferential inhibitor of phosphodiesterase 4B (PDE4B). [3] As it has not been approved for use, safety and efficacy have not been established. It is being investigated as part of the FIBRONEER™ global program, which includes two Phase III studies —FIBRONEER™-IPF [4] in people living with IPF and FIBRONEER™-ILD [5] in people living with progressive pulmonary fibrosis (PPF). Based on these results, Boehringer Ingelheim will submit a new drug application for nerandomilast for the treatment of PPF to the US FDA and other health authorities worldwide. 'The positive FIBRONEER™-ILD topline result shows the potential of nerandomilast in progressive pulmonary fibrosis. The hope is that the safety and tolerability profile we are initially seeing could potentially help to reduce treatment challenges,' said Shashank Deshpande, Head of Human Pharma and Member of the Board of Managing Directors at Boehringer Ingelheim. 'The recent milestones of the FIBRONEER™ trial program underscore our commitment to transforming the lives of patients with this debilitating disease, and are a testament to Boehringer Ingelheim's position at the forefront of pulmonary fibrosis research.' About FIBRONEER™-ILD ( NCT05321082 )5 FIBRONEER™-ILD was a double-blind, randomized, placebo-controlled trial evaluating the efficacy and safety of nerandomilast (BI 1015550) over at least 52 weeks in patients with PPF. Primary endpoint: Absolute change from baseline in FVC (mL) at week 52. Key secondary endpoint: Time to the first occurrence of any of the components of the composite endpoint: time to first acute interstitial lung disease (ILD) exacerbation; first hospitalization for respiratory cause; or death (whichever occurs first) over the duration of the trial. Patients participating in the FIBRONEER™-ILD trial were treated with either oral nerandomilast 9 mg or 18 mg, or placebo, twice-daily, over at least 52 weeks. The 18 mg twice-daily dose of nerandomilast is supported by the results from the Phase II study.2 An additional 9 mg twice-daily dose of nerandomilast was added to evaluate the benefit-risk profile at a lower dose, as well as to provide further dose-response and exposure-response data.2 The trial has been conducted in more than 40 countries, more than 400 locations, and enrolled 1178 patients. About the FIBRONEER™ clinical program: The FIBRONEER™ program includes two Phase III randomized, double-blind, placebo-controlled trials — FIBRONEER™-IPF ( NCT05321069 )4 and FIBRONEER™-ILD ( NCT05321082 )5 — to investigate the efficacy, safety and tolerability of nerandomilast over at least 52 weeks in patients with IPF and in patients with PPF. In both trials, the primary endpoint is the absolute change from baseline in FVC (mL) at week 52.4,5 The key secondary endpoint is the time to the first occurrence of any of the components of the composite endpoint: time to first acute IPF/ILD exacerbation, first hospitalization for respiratory cause, or death (whichever occurs first) over the duration of the trials. About nerandomilast: Nerandomilast (BI 1015550) is an investigational oral, preferential inhibitor of phosphodiesterase 4B (PDE4B) that is being studied as a potential treatment for IPF and PPF.3,4,5 This compound is an investigational agent and has not been approved for use. The efficacy and safety of this investigational compound has not been established. Nerandomilast was granted FDA Breakthrough Therapy Designation for the treatment of IPF in February 2022. [6] The efficacy, safety, and tolerability of nerandomilast was studied in a Phase II randomized, double-blind, placebo-controlled trial of patients with IPF (n=147).3 The primary endpoint was a change from baseline in FVC (a measure of lung function) over a 12-week treatment period.3 About IPF and PPF: IPF is one of the more common progressive fibrosing interstitial lung diseases (ILD). [7] Symptoms of IPF include breathlessness during activity, a dry and persistent cough, fatigue and weakness. [8] Although considered 'rare,' IPF affects approximately 3 million people worldwide.8, [9] The disease primarily affects patients over the age of 50 and affects more men than women.8 Patients with certain types of non-IPF fibrosing ILD may also develop a progressive phenotype known as PPF. In ILDs other than IPF, progressive pulmonary fibrosis is defined by worsening respiratory symptoms, physiological evidence of disease progression and radiological evidence of disease progression. [10] Progressive pulmonary fibrosis can cause irreversible lung damage and lead to early mortality.10, [11] About Boehringer Ingelheim: Boehringer Ingelheim is a biopharmaceutical company active in both human and animal health. As one of the industry's top investors in research and development, the company focuses on developing innovative therapies that can improve and extend lives in areas of high unmet medical need. Independent since its foundation in 1885, Boehringer takes a long-term perspective, embedding sustainability along the entire value chain. More than 53,500 employees serve over 130 markets to build a healthier, more sustainable, and equitable tomorrow.

Boehringer Ingelheim Launches Fast-acting Stroke Medication in the UAE, Reducing Treatment Administration to Five Seconds
Boehringer Ingelheim Launches Fast-acting Stroke Medication in the UAE, Reducing Treatment Administration to Five Seconds

Mid East Info

time28-02-2025

  • Mid East Info

Boehringer Ingelheim Launches Fast-acting Stroke Medication in the UAE, Reducing Treatment Administration to Five Seconds

The newly approved treatment provides a fast-acting option for acute ischemic stroke (AIS) care. Administered as a single IV bolus over a period of five to ten seconds, the treatment offers a significant improvement over regular one-hour-long treatments. Dubai, United Arab Emirates – February 2025: Boehringer Ingelheim, a leading research-driven biopharmaceutical company, has launched a new acute ischemic stroke (AIS) medication with active ingredient Tenecteplase 25mg to enhance emergency stroke treatment in the UAE, offering a faster and more effective treatment option for emergency stroke care. Launched in the UAE for the first time across the India, Middle East, Turkey and Africa region, the new medication can be delivered over five to ten seconds, compared to the previous treatments requiring a one-hour administration process. This simplified and rapid approach facilitates faster treatment administration in emergency settings, reducing both door-to-needle (DTN) times and door-in-door-out (DIDO) times. This can improve patient recovery outcomes and minimize long-term neurological deficits associated with stroke [i] . Stroke is the second leading cause of death globally and a major contributor to disability, thereby imposing significant burdens on both patients and the economy [ii] . Many survivors face long-term disabilities, with up to 50% being chronically disabled [iii] . In the UAE, between 8,000 to 10,000 individuals suffer from a stroke each year, which amounts to one case every hour [iv] . Ischemic strokes occur when there is a blockage in a blood vessel, resulting in reduced blood supply to the brain [v] . Early recognition of symptoms is crucial for effective treatment. Common signs include sudden numbness or weakness, especially on one side of the body; confusion or trouble speaking; difficulty seeing in one or both eyes; dizziness or loss of balance; and a severe headache with no known cause [vi] . The new medication was launched on 22 February during the 5th Dubai Neurology Congress, which brought together over 120 healthcare professionals from the UAE. Dr. Suhail Al Rukn, President of the Emirates Neurology Society and Consultant Neurologist highlighted the importance of time efficiency in stroke care. 'Time is brain,' Dr. Al Rukn said. 'Reducing the time between symptoms onset and treatment is crucial in saving lives and preserving brain function [vii] . For every minute that treatment is delayed, millions of brain cells are lost [viii] . Seeking immediate medical care can therefore greatly improve outcomes and minimize the risk of long-term disability. This new treatment offers a major leap forward by minimizing delays and simplifying the administration process, providing an opportunity to improve outcomes for stroke patients in the UAE.' Ousama Alhaj, General Manager and Head of Human Pharma, Boehringer Ingelheim in the Near East and UAE added: 'The UAE, like many other countries around the world, faces a growing incidence of stroke cases each year [ix] , making timely treatment a priority. This new medication not only improves the efficiency of care delivery but also enhances the overall healthcare journey for patients. At Boehringer Ingelheim, we are committed to developing patient-centered health solutions that improve survival rates and long-term outcomes for stroke patients. We also remain committed to working closely with healthcare stakeholders to ensure these medications are accessible to those who need them.' Administered at a dose of 0.25mg/kg (up to a maximum of 25mg) as a single intravenous bolus, the new treatment is now available in the UAE and underscores Boehringer Ingelheim's ongoing dedication to patient-centered innovation in healthcare, with a focus on early detection, prevention, and treatment. The company continues to strengthen its presence in the UAE by providing advanced medical solutions that address the needs of healthcare professionals and patients alike. About Boehringer Ingelheim: Boehringer Ingelheim is working on breakthrough therapies that improve the lives of humans and animals. As a leading research-driven biopharmaceutical company, the company creates value through innovation in areas of high unmet medical need. Founded in 1885 and family-owned ever since, Boehringer Ingelheim takes a long-term perspective. Around 52,000 employees serve more than 130 markets in the three business areas, Human Pharma, Animal Health, and Biopharmaceutical Contract Manufacturing.

DOWNLOAD THE APP

Get Started Now: Download the App

Ready to dive into the world of global news and events? Download our app today from your preferred app store and start exploring.
app-storeplay-store