Date : 05 February 2026

Headquarter: Switzerland
Latest Update: In December 2025, Roche announced that the U.S. Food and Drug Administration (FDA) had approved additional indications for its PATHWAY anti-HER2/neu (4B5) Rabbit Monoclonal Primary Antibody and VENTANA HER2 Dual ISH DNA Probe Cocktail tests.
Headquarter: United States
Latest Update: In October 2025, AbbVie announced it would unveil novel data from its vigorous antibody-drug conjugate (ADC) platform at the 2025 European Society for Medical Oncology (ESMO) congress.
Headquarter: United States
Latest Update: In April 2025, Amgen announced that the U.S. Food and Drug Administration (FDA) had approved UPLIZNA as the first and only treatment for adults living with Immunoglobulin G4-related disease (IgG4-RD).
Headquarter: United States
Latest Update: In April 2025, Johnson & Johnson announced that the U.S. Food and Drug Administration (FDA) had approved IMAAVY, a human FcRn-blocking monoclonal antibody, for the management of generalized myasthenia gravis (gMG).
Headquarter: United States
Latest Update: In December 2025, Harbour BioMed announced a multi-year, global strategic partnership and license agreement with Bristol Myers Squibb to discover and develop next-generation many-specific antibodies.
Headquarter: United States
Latest Update: In October 2025, Merck announced it had initiated three Phase 2b trials evaluating the safety and efficacy of tulisokibart, an investigational humanized monoclonal antibody targeting tumor necrosis factor (TNF)-driven cytokine 1A (TL1A).
The global humanized monoclonal antibody market size was estimated at USD 170.04 billion in 2025 and is predicted to increase from USD 190.34 billion in 2026 to approximately USD 525.3 billion by 2035, expanding at a CAGR of 11.94% from 2026 to 2035.

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