Pipeline
Transforming Biological Insight into Promising Drug Candidates
- Discovery
- Preclinical
- Phase 1
- Phase 2
- Phase 3
- Filed / Approved *
- Therapeutic Area: Cardiology
- Indication: ATTR Cardiomyopathy
- Product Candidate: Cliramitug (formerly ALXN2220, NI006)
- Target: TTR amyloid
- Modality: mAb
- Partner: AstraZeneca
Cliramitug (formerly ALXN2220, NI006), is a human antibody that exclusively targets with high affinity the disease-associated amyloid conformation but not physiological forms of transthyretin. Cliramitug targets both wild-type ATTR as well as ATTR mutants that are linked to hereditary forms of ATTR cardiomyopathy (ATTR-CM) and ATTR polyneuropathy. Cliramitug induces the clearance of pathological ATTR in preclinical models. Currently, Cliramitug is in Phase 3 clinical development (NCT06183931). The U.S. Food and Drug Administration (FDA) has granted Alexion, AstraZeneca Rare Disease Fast Track designation for the development of ALXN2220 for the treatment of ATTR-CM.
In 2022, Neurimmune entered into an exclusive global collaboration and license agreement with Alexion, AstraZeneca’s Rare Disease group, to develop Cliramitug.
- Therapeutic Area: CNS
- Indication: Amyotrophic Lateral Sclerosis
- Product Candidate: AP-101
- Target: misfolded SOD1
- Modality: mAb
- Partner: TVM
AP-101 is a recombinant human antibody designed to selectively deplete toxic, misfolded forms of SOD1 while preserving the protective function of physiological SOD1. By targeting only the pathological conformations, AP-101 aims to disrupt a key driver of ALS progression without lowering total SOD1 levels. Neurimmune and TVM Capital Life Science co-created AL-S Pharma to develop AP-101. AL-S Pharma has executed its innovative clinical plan for AP-101 in collaboration with an international network of ALS experts.
- Therapeutic Area: CNS
- Indication: Alzheimer's Disease
- Product Candidate: NSC001
- Target: muscarinic M1 receptor
- Modality: small molecule
- Partner: NSC Therapeutics
NSC001 is developed by Neurimmune’s collaboration partner NSC Therapeutics GmbH. It is a small, rigid, chemical analog of the cholinergic neurotransmitter acetylcholine in development for the treatment of patients with cholinergic deficits. NSC Therapeutics GmbH received $5 mio funding from the Alzheimer’s Disease Drug Discovery Foundation to support upcoming Phase 2 proof of concept clinical trials.
- Therapeutic Area: CNS
- Indication: Spinal Cord Injury
- Product Candidate: NG004
- Target: Nogo-A
- Modality: mAb
- Partner: Novago
NG004 is a human antibody blocking the function of Nogo-A, one of the most potent and well-studied nerve growth inhibitors. NG004 is developed by NovaGo Therapeutics for the treatment of spinal cord injury. Novago Therapeutics is a spin-off company from the University of Zurich that entered into a strategic partnership with Neurimmune to discover human antibodies targeting Nogo-A. NovaGo Therapeutics was founded by Prof. Martin Schwab based on the discovery of the existence of “inhibitors of nerve fiber growth” as a cause of the absence of regeneration of injured fiber tracts in the central nervous system.
- Therapeutic Area: CVM
- Indication: AL Amyloidosis
- Product Candidate: NI009
- Modality: mAb
- Partner: AstraZeneca
NI009 is human monoclonal antibody designed to target and deplete light chain fibrils and deposits from affected tissues and organs in light chain (AL) amyloidosis.
- Therapeutic Area: CNS
- Indication: Neurodegeneration
- Product Candidate: NI504
- Modality: mAb
- Partner: Ono
- Therapeutic Area: CNS
- Indication: Alzheimer's Disease
- Product Candidate: NI101B3
- Target: Brain amyloid
- Modality: Bispecific antibody
NI101B3 is a next generation amyloid beta targeting antibody with improved penetration of the blood brain barrier.
- Therapeutic Area: Cardiology & CNS
- Indication: Protein Aggregation Diseases