Bifogade filer
Beskrivning
Land | Danmark |
---|---|
Lista | Large Cap Copenhagen |
Sektor | Hälsovård |
Industri | Läkemedel & Handel |
· The HOPE trial met its primary endpoint in migraine prevention, demonstrating that patients treated with Lu AG09222 had a statistically significantly greater reduction in number of monthly migraine days (MMDs) from baseline to weeks 1 to 4 of treatment compared to placebo.
- Lu AG09222 was well tolerated
Valby, Denmark, April 19, 2023 - H. Lundbeck A/S (Lundbeck) announced positive results of the HOPE trial, a clinical proof of concept trial of Lu AG09222 as a potential treatment for the prevention of migraine (NCT05133323). The primary analysis concluded that there was a statistically significant difference (p=0.01) between Lu AG09222 and placebo in the mean change from baseline in the number of monthly migraine days over weeks 1 to 4.
The phase IIa double-blind, placebo-controlled trial of Lu AG09222 was designed to assess the efficacy, safety, and tolerability of a single intravenous infusion of Lu AG09222. The trial consisted of a 4-week, double-blind treatment period, and an 8-week follow-up period after the last dose. A total of 237 patients were randomized in the trial.
Lu AG09222 is an investigational monoclonal antibody (mAb) that is designed to bind and inhibit signaling mediated by pituitary adenylate cyclase-activating polypeptide (PACAP); a neuropeptide that is implicated in migraine pathophysiology.
Lu AG09222 represents a potential new therapeutic option, targeting a pathway in migraine that is distinct from the recently available calcitonin gene-related peptide (CGRP) migraine treatment drug class.
Dr. Johan Luthman, EVP and Head of Research & Development in Lundbeck, said:
"This is the first investigational compound targeting PACAP that has demonstrated efficacy in a migraine prevention trial. Based on this positive outcome, Lu AG09222 will progress into further development. With its novel mechanism of action, it has the potential to become an important addition to Lundbeck's migraine portfolio, augmenting our efforts in helping patients with migraine and potentially other pain related indications globally."
Full trial results are not yet available. Further prespecified and exploratory analyses of the data set will be conducted to determine the potential of Lu AG09222 in the prevention of migraine in adult patients.
Lu AG09222 was generally well tolerated.
Lundbeck is grateful to all the patients with migraine, and the investigators who participated in the trial and contributed greatly to this research.
The trial results are planned to be submitted for scientific publication at a later date.
Lundbeck will discuss the further clinical development plan with regulatory authorities.
About the phase II migraine trial
The HOPE trial was an interventional, multi-national, multi-site, randomized, double-blind, parallel-group, placebo-controlled phase IIa trial designed to assess the safety, tolerability and efficacy of a single intravenous infusion of Lu AG09222 for the prevention of migraine in patients that had failed prior treatments. The trial consisted of a 4-week double-blind treatment period with a follow-up period for 8 weeks. The primary endpoint was the change from baseline in the number of monthly migraine days over weeks 1 to 4, compared to placebo. Secondary endpoints were ≥50% reduction from baseline in MMDs (Weeks 1 to 4) and change from baseline in the number of monthly headache days (Weeks 1 to 4), compared to placebo.
The target population for this trial was defined as patients diagnosed with migraine as outlined in the International Classification of Headache Disorders Third Edition (ICHD-3) with unsuccessful prior preventive treatments A total of 237 patients, recruited from specialist settings, were randomly allocated via a randomization system to one of three treatment groups: two doses of Lu AG09222 or placebo.
About Lu AG09222
Lundbeck is developing Lu AG09222, an investigational monoclonal antibody (mAb) designed to bind and inhibit pituitary adenylate cyclase-activating polypeptide (PACAP)[i]. PACAP has emerged as a neuropeptide implicated in the pathophysiology of migraine and represents a novel target in migraine. Lu AG09222 represents a potential new therapeutic option, targeting a pathway in migraine that is distinct from the recently available calcitonin gene-related peptide (CGRP) migraine treatment drug class.
About migraine
Migraine is a complex and incapacitating neurological disease characterized by recurrent episodes of moderate to severe, pulsating headaches typically accompanied by an array of symptoms, including nausea, vomiting, and sensitivity to light and sound[ii]. As the most prevalent neurological disorder in people aged <50 years, migraine imposes both a social and financial burden, affecting around 135 million people in the G7 countries plus China. Repeated migraine attacks, and often the constant fear of the next one, damage family life, social life and work life[iii].
Lundbeck contacts
Investors: Media:
Palle Holm Olesen Thomas Mikkel Mortensen
Vice President, Investor Relations Media Relations Lead, Corp. Communication
PALO@lundbeck.com THMR@lundbeck.com (thmr@lundbeck.com)
+45 30 83 24 26 +45 30 83 30 24
About H. Lundbeck A/S
Lundbeck is a global pharmaceutical company specialized in brain diseases. For more than 70 years, we have been at the forefront of neuroscience research. We are tirelessly dedicated to restoring brain health, so every person can be their best. We are committed to fighting stigma and discrimination against people living with brain diseases and advocating for broader social acceptance of people with brain health conditions. Our research programs tackle some of the most complex challenges in neuroscience, and our pipeline is focused on bringing forward transformative treatments for brain diseases for which there are few, if any therapeutic options.
For additional information, we encourage you to visit our corporate site www.lundbeck.com and connect with us on Instagram (h_lundbeck), Twitter at @Lundbeck andvia LinkedIn.
Safe Harbor/Forward-Looking Statements
This corporate release contains forward-looking statements that provide our expectations or forecasts of future events such as new product introductions, product approvals and financial performance. Forward looking statements include, without limitation, any statement that may predict, forecast, indicate or imply future results, performance or achievements, and may contain words like "believe", "anticipate", "expect", "estimate", "intend", "plan", "project", "will be", "will continue", "will result", "could", "may", "might", or any variations of such words or other words with similar meanings. All statements other than statements of historical facts included in this presentation, including, without limitation, those regarding our financial position, business strategy, plans and objectives of management for future operations (including development plans and objectives relating to our products), are forward looking statements.
Such forward looking statements involve known and unknown risks, uncertainties and other factors which may cause our actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by such forward looking statements. Factors that may affect future results include, among others, interest rate and currency exchange rate fluctuations, delay or failure of development projects, production or distribution problems, unexpected contract breaches or terminations, government-mandated or market-driven price decreases for Lundbeck's products, introduction of competing products, Lundbeck's ability to successfully market both new and existing products, exposure to product liability and other lawsuits, changes in reimbursement rules and governmental laws and related interpretation thereof, and unexpected growth in costs and expenses.
The forward-looking statements in this document and oral presentations made on behalf of Lundbeck speak only as at the date of this presentation. Lundbeck does not undertake any obligation to update or revise forward-looking statements in this presentation or oral presentations made on behalf of Lundbeck, nor to confirm such statements to reflect subsequent events or circumstances after the date of the presentation or in relation to actual results, unless otherwise required by applicable law or applicable stock exchange regulations.
[i] Moldovan Loomis, C., et al., Pharmacologic Characterization of ALD1910, a Potent Humanized Monoclonal Antibody against the Pituitary Adenylate Cyclase-Activating Peptide. J Pharmacol Exp Ther, 2019. 369(1): p. 26-36
[ii] Headache Classification Committee of the International Headache Society (IHS). The International Classification of Headache Disorders, 3rd Edition. Cephalalgia, 2018. 38(1): p. 1-211.
[iii] Burch, R.C., D.C. Buse, and R.B. Lipton, Migraine: epidemiology, burden, and comorbidity. Neurol Clin, 2019. 37(4): p. 631-649.