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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. 
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.

Eptinezumab (anti-CGRP mAb) Episodic 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.

Brexpiprazole* Agitation in Alzheimer's disease 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 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.

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 symptomatology with re-experiencing, Negative cognition and mood, Avoidance and Arousal.

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

Brexpiprazole* Borderline Personality DIsorder 2

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. Serotonergic and Dopaminergic stabilization may directly address the pathways implicated in the BPD features of impulse aggression (SER), and emotional dysregulation, impulsivity, and cognitive disturbances (DA).

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

Aripiprazole 2-month injectable* Schizophrenia + Bipolar I Disorder 1

Wirkungsart

Aripiprazole is a small molecule. It acts as a partial agonist at dopamine D2 and serotonin 5-HT1A receptors and antagonist at serotonin 5-HT2A receptors. A 2-month formulation will serve as a treatment option when treating patients with Schizophrenia or Bipolar I disorder where long-acting treatment is needed.

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

Lu AG06466 (MAGL inhibitor)* PTSD 1

Wirkungsart

Lu AG06466 is a small molecule expected to be highly brain-penetrant. Lu AG06466 is a highly selective inhibitor 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 may produce beneficial effects across a range of symptoms including stress, anxiety and hyperarousal; symptoms which are relevant to PTSD.

*MAGL: Monoacylglycerol lipase. PTSD study has been initiated, additional phase 1b studies within psychiatry/neurology will be explored during 2021.

Lu AG06479 (MAGL inhibitor)* Neurology, Psychiatry 1

Wirkungsart

Lu AG06479 is a small molecule expected to be highly brain-penetrant. Lu AG06466 is a highly selective inhibitor of monoacylglycerol lipase (MAGL), the primary enzyme responsible for the degradation of the endocannabinoid ligand 2-arachidonoylglycerol (2-AG). Enhancing 2-AG levels is a viable approach to restore brain homeostasis.

*MAGL: Monoacylglycerol lipase. PTSD study has been initiated, additional phase 1b studies within psychiatry/neurology will be explored during 2021.

Lu AF82422 (alpha-synuclein mAb) Synucleinopathies 1

Wirkungsart

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

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.

Lu AG09222 (PACAP mAb)* Migraine 1

Wirkungsart

LU AG09222 is a monoclonal antibody designed to inhibit pituitary adenylate cyclase-activating polypeptide (PACAP) signaling for migraine prevention. PACAP has emerged as a signaling molecule in the pathophysiology of migraine.

*PACAP: Pituitary adenylate cyclase-activating polypeptide

Lu AF87908 (Tau mAb) Tauopathies 1

Wirkungsart

Lu AF87908 (Tau mAb) is a monoclonal antibody targeting the pathological form of the protein tau which is believed to play a pivotal role in the development and progression of Alzheimer’s disease and other neurodegenerative disorders.

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.