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REAL-TIME GLOBAL RESEARCH

Quick Deep Dive: We Like the STAR Deal, but INCY Valuation Still Full *SLIDES*

Published: 2026-06-17Institution: JefferiesPages: 40Original language: EnglishEvidence page: 1

Research evidence excerpt

Quick Deep Dive: We Like the STAR Deal, but INCY Valuation Still Full *SLIDES*

life limitation

Efficacy looks good: 81% ABR reduction (in naive pts) and 75-100% in switch pts >> comps•

well vs approved tx

PK supports much better dosing vs conventional tx: ~1-mo half-life supports Q4W SC dosing•

Safety something to consider: Safe and well-tolerated so far, but theoretical risk is Protein S•

inhibition LT may increase thrombosis risk.

Exhibit 1 - Competitive Landscape in Von Willebrand (VWD) Prophylaxis (Prophy)

Wilate Vonvendi HMB-002 VGA039

Company Octapharma Takeda Hemab Incyte

US Launch year 2010 2016 In Ph1/2 In Ph3

Target population Broad VWD Broad VWD Broad VWD Severe and persistent bleeding

Clinical trial NCT04053699 and NCT04052698 NCT02973087 NCT06754852 NCT05776069

Monovalent IgG4 antibody that binds VWF CK

VWF/FVIII concentrate replacing deficient VWF Replacement therapy to restore deficient protein domain to protect from clearance and stabilize Fully human IgG4 monoclonal antibody targeting

MoA and stabilizing FVIII to restore hemostasis levels FVIII Protein S to enhance thrombin generation

Median 81%2 ABR reduction in pts w/out prior IV

prophylaxis;

Efficacy (ABR TBD (demonstrated >1.5-fold increase in VWF 75%-100% in pts switching from prior IV

reduction) 84% reduction 92% reduction1 and FVIII levels (clinical benchmark)) prophylaxis

Prophy dosing 2–3 IV infusions per week; On-demand: As

frequency IV 2–3 times per week needed per bleed TBD (from weekly to monthly SubQ) Once-monthly subcutaneous injection

Thrombosis risk (FVIII accumulation),

Safety (pot'l) hypersensitivity, minimal pathogen transmission Generally well-tolerated; primary risks include Elevated D-dimer levels and venous thrombosis Concerns regarding thrombotic risk due to

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