Sprache

Sie verlassen Lundbeck Schweiz

Sie verlassen jetzt lundbeck.com/ch. Bitte beachten Sie, dass die Informationen auf der Seite, auf die Sie verlinkt werden, möglicherweise nicht in vollem Umfang mit den gesetzlichen Bestimmungen in der Schweiz, sowie die produktbezogenen Informationen mit den entsprechenden schweizer Fachinformationen für Arzneimittel  übereinstimmen. Alle Informationen sollten mit Ihrem Arzt besprochen werden und ersetzen nicht die Beratung und Behandlung durch Ihren Arzt.

sie werden weitergeleitet zu

Zurück

Pipeline

Neuentwicklung

Unsere Forschungs- und Entwicklungsabteilung sucht und entdeckt neue Ansatzpunkte, um Gehirmerkrankungen zu bekämpfen. Gemeinsam arbeiten wir an dem Ziel, Patienten Therapien zur Verfügung zu stellen, die den Behandlungsstand neu definieren und dort die Versorgung verbessern, wo die Not am größten ist. 
Hormonal / neuropeptide signaling
Projekt Forschungsgebiet Phase 1 Phase 2 Phase 3 Produktion
Eptinezumab (anti-CGRP mAb)* Migraine prevention Filing

Wirkungsart

Eptinezumab is a monoclonal immunoglobulin G1 (IgG1) antibody that binds to human calcitonin gene-related peptide (CGRP) with high specificity and high affinity for the CGRP α- and β-form. CGRP is a signaling molecule in the pathophysiology of migraine and cluster headache.

*Three phase III clinical trials (SUNLIGHT, SUNRISE, and SUNSET) are related to the Asia registration activities.

Eptinezumab (anti-CGRP mAb) Cluster headache 3

Wirkungsart

Eptinezumab is a monoclonal immunoglobulin G1 (IgG1) antibody that binds to human calcitonin gene-related peptide (CGRP) with high specificity and high affinity for the CGRP α- and β-form. CGRP is a signaling molecule in the pathophysiology of migraine and cluster headache.

Lu AG09222 (anti-PACAP mAb) Migraine prevention 2

Wirkungsart

Lu AG09222 is an investigational monoclonal antibody designed to bind and inhibit signaling mediated by pituitary adenylate cyclase-activating polypeptide (PACAP); a neuropeptide that is implicated in migraine pathophysiology.

Lu AG13909 (anti-ACTH mAb) Neurohormonal dysfunctions 1

Wirkungsart

Lu AG13909 is a humanized anti-adrenocorticotropic hormone (anti-ACTH) monoclonal antibody that blocks the binding of ACTH to the melanocortin 2 receptor in the adrenal glands, thereby decreasing the neurohormonal signaling of ACTH.

Circuitry / neuronal biology
Projekt Forschungsgebiet Phase 1 Phase 2 Phase 3 Produktion
Aripiprazole 2-month injectable* Schizophrenia + Bipolar I disorder Filing

Wirkungsart

A 2-month injectable aripiprazole formulation in an extended dosing interval has the potential to improve adherence to treatment and provide continuous exposure to medication, relevant to the clinical outcomes in adult patients with schizophrenia or BP-I. 

*Clinical program finalized; Lundbeck and Otsuka Pharmaceutical have submitted the aripiprazole 2-month injectable formulation to the European Medicines Agency (EMA) for marketing authorization application (MAA) review and as well as to the US Food & Drug Administration (FDA). 

Is approved in the U.S.

Brexpiprazole* Agitation in Alzheimer's disease (AADAD) Filing

Wirkungsart

Brexpiprazole is a small molecule and a potent serotonin–dopamine activity modulator. It acts as a partial agonist at serotonin 5-HT1A and dopamine D2 receptors, and as an antagonist at serotonin 5-HT2A and noradrenaline α1B/α2C receptors. The serotonin, dopamine, and noradrenaline neurotransmitter systems may be implicated in behavioral symptoms of dementia, including agitation.

*Life cycle management. In partnership with Otsuka Pharmaceutical Development & Commercialization, Inc.

AADAD: Agitation Associated with Dementia due to Alzheimer’s Disease.

Is approved in the U.S.

Brexpiprazole* PTSD 3

Wirkungsart

Brexpiprazole is a small molecule and a potent serotonin–dopamine activity modulator. It acts as a partial agonist at serotonin 5-HT1A and dopamine D2 receptors, and as an antagonist at serotonin 5-HT2A and noradrenaline α1B/α2C receptors. The serotonergic, dopaminergic, and especially the noradrenergic systems are believed to be involved in PTSD (post-traumatic stress disorder) symptomatology with re-experiencing, Negative cognition and mood, Avoidance and Arousal.

*Life cycle management. In partnership with Otsuka Pharmaceutical Development & Commercialization, Inc.

Lu AF28996 (D1-D2 agonist) Parkinson's disease 1

Wirkungsart

Lu AF28996 is a small molecule with agonistic properties towards D1 and D2 receptors. Concerted D1 and D2 dopamine receptor stimulation may play an important role in motor control of Parkinson’s disease patients.

MAGLi program Psychiatry + Neurology 1

Wirkungsart

The MAGL inhibitor program consists of several small molecules and highly selective inhibitors of monoacylglycerol lipase (MAGL), the primary enzyme responsible for the degradation of the endocannabinoid ligand 2-arachidonoylglycerol (2-AG). Enhancing the actions of 2-AG on CB1 and CB2 receptors may restore altered neuronal transmission and decrease neuroinflammation and thereby it may produce beneficial effects across a range of symptoms and related indications within Neurology and Psychiatry.

Protein aggregation, folding and clearance
Projekt Forschungsgebiet Phase 1 Phase 2 Phase 3
Lu AF82422 (anti-alpha-synuclein mAb) Synucleinopathies (MSA) 2

Wirkungsart

Lu AF82422 is a monoclonal antibody (mAb) targeting alpha-synuclein. Misfolding, aggregation and extracellular spreading of alpha-synuclein is believed to play a major role in disease pathology and progression in Multiple System Atrophy (MSA), Parkinson’s disease and other neurodegenerative disorders.

Neuroinflammation / Neuroimmunology
Projekt Forschungsgebiet Phase 1 Phase 2 Phase 3
Lu AG22515 (CD40L blocker)* Neurology 1

Wirkungsart

Lu AG22515 is a CD40L blocker, which interferes with the activation of the adaptive immune response by inhibiting the CD40L/CD40 co-stimulatory interaction on immune cells; an interaction, which plays a role in the pathophysiology of several immune-mediated diseases.

* CD40L/serum-albumin bispecific antibody-fragment ((scFv)2-Fab)) based on AprilBio’s SAFA™ technology platform.

mehr über Lundbeck

Forschung & Entwicklung

Die Forschung und Entwicklung von neuen und verbesserten Behandlungsmethoden ist der Kern unserer Arbeit.

Geschäftsentwicklung

Partnerschaften sind ein wichtiger Pfeiler in unserer Strategie, führend im Bereich der Gehirngesundheit zu werden.

Gehirnerkrankungen verstehen

Die Weg zur Gehirngesundheit beginnt mit dem Verständnis der Krankheiten im Gehirn.