Developing the best MATCH for patients through plug & play assembly of novel multispecific biotherapeutics.

Establishing leading platform of next generation plug & play novel multispecific therapeutics.

Advancing a proprietary pipeline of next generation immunology and immuno-oncology drugs.

News

Numab Therapeutics Announces Series C Extension to CHF 180 Million, Completing Oversubscribed CHF 50 Million Financing Read more

Pipeline

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Overcoming limitations of existing approaches to uncover vast potential for new medicines

Our proprietary platforms λ-Cap™ and MATCH™ are designed to create differentiated therapeutics on a repeatable basis. Using a novel, rational process, our discovery and engineering technology yields multispecific antibody-based therapeutics with tailored pharmacokinetic properties that improve on first-generation antibody therapies in terms of potency, stability, effect duration, and safety. Alongside our own in-house pipeline programs we have a number of strong discovery and development partnerships with pharma and biotech.

Spearheading the development of first- and best-in-class high-impact therapeutics

We use validated discovery and engineering technologies to improve the predictability of the drug discovery process. We are establishing a proprietary pipeline of highly differentiated therapeutics by targeting clinically validated pathways with multispecific molecules to create novel mechanisms of action designed to overcome the limitations of existing approaches and differentiate from standard of care by superior efficacy and favorable safety.

Advancing our lead program NM26, a bispecific antibody targeting IL-4Rα (type I and type II receptors) and IL-31 for the treatment of atopic dermatitis and other type 2 inflammatory disorders

NM26-2198 is designed to prevent IL-4/IL-13 and IL-31-induced keratinocyte immunopathology, immune cell activation, skin barrier function impairment and pruritis, all of which are hallmarks of the pathophysiology of atopic dermatitis (AD). The targeting of the IL-4/IL-13 pathway is well established for the treatment of AD and other inflammatory diseases. We believe that adding IL-31 mediated blockade of neuroinflammation to the repression of Th2 driven inflammation by IL-4/IL-13 blockade could enable a faster onset of action and improved efficacy compared to the current standard of care in AD, together with convenient subcutaneous administration. Atopic Dermatitis still has a high unmet medical need and represents a multi-billion-dollar market opportunity. Numab develops this program together with Kaken Pharmaceutical Co., Ltd, our regional partner in Japan.

Latest News

January 09, 2025 Numab Therapeutics Announces Series C Extension to CHF 180 Million, Completing Oversubscribed CHF 50 Million Financing

CHF 50 Million extension round co-led by Cormorant Asset Management, with participation from other existing investors.
Proceeds will be used to support the advancement of multiple first-in-class and best-in-class programs into clinical development.

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November 15, 2024 Numab Therapeutics and Kaken Pharmaceutical Enter Collaboration and Option Agreement for Multi-specific Antibody ND081 for Treatment of Inflammatory Bowel Disease

Numab to receive R&D funding for the preclinical development of ND081.
Kaken Pharmaceutical receives an option to in-license ND081 in certain Asian territories in exchange for funding global development up to clinical POC.

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October 30, 2024 Numab Therapeutics Announces Initiation of Phase 1 Clinical Study of NM32 Program in Patients with Solid Tumors

NM32 is a first-in-class half-life-enhanced T-cell engager targeting ROR1, a tumor associated antigen with broad expression in solid tumors and hematological malignancies.
Low molecular weight of NM32 allows to efficiently achieve higher tumor concentrations than larger immunoglobulin G molecules, the current standard format for CD3 engagers.

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