Committed to Improving Lives of People Living with Autoimmune Diseases
May 2026
Advancing to Immune Reset
Evolving to deliver more value for patientsClinical response
Deeper clinical response
(with more patients achieving remission)
Disease modification
Long-lasting drug-free remission
Complete restoration of health and resolution of damage
Proprietary and Confidential Property of UCB
UCB's ambition is to become a leader in immune reset, restoring immune balance and enabling deep, durable, treatment-free remission across autoimmune diseases | |
Combining internal innovation, licensing, and acquisitions to build a scalable T-cell engager platform, reinforcing long-term immune-disease ambition | |
Cizutamig, in multiple Phase 1 studies, is positioned as a potential best-in-class BCMA × CD3 T-cell engager for autoimmune diseases, enabling targeted T-cell-mediated B-cell cytotoxicity, while mitigating cytokine release and ICANS | |
Together with Antengene license, this acquisition is set to broaden UCB's reach across multiple B-cell targets and disease mechanisms, strengthening innovative immune-reset breadth |
potential cure
INFLAMMATION SUPPRESSION
RESOLUTION OF INFLAMMATION
IMMUNE RESET
Note: BCMA = B cell maturation antigen; CD3 = Cluster of Differentiation ; TCE = T-Cell Engager; ICANS = Immune Effector Cell-Associated Neurotoxicity Syndrome
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Candid TherapeuticsAdvancing Next-Generation Treatments for Autoimmune Diseases
Company Description & Pipeline Overview
HQ: San Diego, CA
Founded in 2024
~50 employees across U.S. and China
Private Company
Drug Candidate | Clinical Focus | Discovery | IND-Enabling | Phase 1 | Phase 2 | Phase 3 |
Cizutamig | Autoantibody autoimmune diseases1 | BCMAxCD3 | ||||
CND261 | Autoimmune diseases2 | CD20xCD3 | ||||
CND319 | Autoimmune diseases | CD19xCD20xCD3 | ||||
CND460 | Autoimmune diseases | BCMAxCD19xCD3 | ||||
Proprietary and Confidential Property of UCB
Note: BCMA = B-cell Maturation Antigen; U.S. = United States
Phase 1 multiple myeloma (MM) completed (40 patients).
Phase 1 Non-Hodgkin's lymphoma (NHL) completed (93 patients). 4
Potential to be a best-in-class BCMA TCE for autoimmune disease
Robust on-target human biology, supported by early clinical efficacy signals
POTENTIAL FOR LEADING POSITION IN
BCMA-TARGETED AUTOIMMUNE THERAPIES
>100 patients evaluated including 68 autoimmune patients across multiple indications in China and Europe.
Proprietary and Confidential Property of UCB
MEANINGFUL EARLY CLINICAL DATASET
CizutamigBCMA x CD3 TCE
Favorable tolerability allowing outpatient dosing1
Favorable safety profile, characterized by predominantly low-grade, manageable CRS and no ICANS
FAVORABLE TOLERABILITY & SAFETY
Early studies across multiple autoimmune diseases (including MG, SLE, RA and SSc-ILD) provide insights into biological activity and dosing strategies2
Planned Global Phase 2 studies in MG and SARD-ILD
Potential to expand development across a range of antibody-mediated autoimmune conditions
MULTI-INDICATION DEVELOPMENT OPPORTUNITY
Note: 1. Candid Therapeutics Plans to Initiate Multiple Phase 2 Studies Following Promising Clinical Data of T-cell Engagers in Autoimmune Diseases - Candid Therapeutics; 2. https://clinicaltrials.gov/; BCMA = B cell maturation antigen; CRS = cytokine release syndrome; ICANS = Immune effector cell-associated neurotoxicity syndrome; ILD = interstitial lung disease; MG = myasthenia gravis: RA = rheumatoid arthritis; RRMM = Relapsed or Refractory Multiple Myeloma: SLE = systemic lupus erythematosus; SARD-ILD =Systemic Autoimmune
Rheumatic Diseases Associated interstitial lung disease; TCE = T-Cell Engager. 5
Accelerating Future GrowthStrategic Rationale for Acquiring Candid Therapeutics
Proprietary and Confidential Property of UCB
Enables a diversified immunology portfolio combining targeted immune reset and broad inflammation control to deliver more durable, biology-driven outcomes in severe immune-mediated diseases
Cizutamig, currently in multiple Phase 1 studies, is positioned as a potential best-in-class BCMA T-cell engager for autoimmune diseases and brings a highly experienced TCE and bispecific antibody development team
+
Candid's BCMA-targeted development strategy has the potential to span multiple diseases characterized by autoantibody-driven pathology offering the opportunity for deep, durable immune reset
Candid provides the opportunity to establish a presence in the field of BCMA-based TCEs and to acquire critical immune-reset experience in B cell depletion across multiple patient populations
Note: BCMA = B-cell Maturation Antigen; TCE = T-Cell Engager
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Compelling Value Proposition for All StakeholdersTerms Upon Closure of the Transaction
Consideration
Upfront of $2bn in cash
Development milestone payments of up to $200mm
Timing
Transaction approved by the Boards of both companies
Closing subject to antitrust clearances and other customary closing conditions
Closing expected by end of Q2 - early Q3 2026
Financial impact
2026 financial impact expected to be manageable within UCB's disciplined framework. Most recent 2026 financial guidance remains unchanged, with revenue expected to grow in a high single-digit to low double-digit percentage range at constant exchange rates (CER). 2026 underlying profitability, measured by adjusted EBITDA, is expected to grow in a high single-digit to mid-teens percentage range (CER)
Proprietary and Confidential Property of UCB
* These expectations exclude the potential impact of U.S. tariffs and any implications related to a Most Favoured Nation (MFN) pricing arrangement, as no final outcomes have been determined at this stage.
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Proprietary and Confidential Property of UCB
For further information:
Investor Relations
investor-relations@ucb.com
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Proprietary and Confidential Property of UCB
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