ROIV
Published on 06/17/2025 at 13:08
Brepocitinib: Investor Event
Seeking to improve the lives of patients with DM and other serious autoimmune conditions
Brepocitinib program overview
Focus on dermatomyositis (DM)
Brepocitinib in the context of Roivant
Q&A
Chief Executive Officer, Roivant
Chief Executive Officer, Priovant
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For investor audiences only
Brepocitinib's VALOR study, if positive, could significantly improve the standard of care for >40K patients currently living with dermatomyositis (DM) and potentially set a new clinical bar for other therapies
Across multiple ongoing studies, if successful, brepocitinib could help >200K patients. ROIV's enthusiasm and confidence drives the speed, depth and breadth of brepocitinib's ongoing & planned late-stage development program (with Phase 3 studies ongoing for NIU and PoC study ongoing in CS)
VALOR's expected readout in 2H25 is the first of several upcoming clinical and regulatory
catalysts expected for brepo over the next 24 months
Note: All drugs are investigational and subject to regulatory approvals. All catalyst timings are based on current expectations and, where applicable, contingent on FDA feedback, and may be subject to change. All references are to calendar years. SoC = Standard of Care
PoC = Proof of Concept
NIU = Non-Infectious Uveitis CS = Cutaneous Sarcoidosis
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For investor audiences only
Evolution of JAK inhibitor field highlights demand for efficacy in treating patients with the most debilitating symptoms
Nonspecific/pan-JAK inhibitors
Single JAK Isoform Inhibitors
First targeted oral agents for inflammatory diseases
Non-specificity limited ability to dose to maximal efficacy and led to class-wide black box warning
Modest commercial success, uptake impaired by less-than-biologic efficacy
Rinvoq (JAK1) is a multi-blockbuster drug (despite a black box warning) on the back of often best-in-indication efficacy
Brepo
Brepo combines the best attributes of selective TYK2 and JAK1 inhibition with potential to provide very robust efficacy for patients across highly morbid, heterogeneous autoimmune diseases
Selective, Dual Inhibitor of TYK2 and JAK1
Sotyktu (TYK2), designed specifically to avoid black box liability, has underperformed commercially due to less-than-biologic efficacy
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For investor audiences only
Disclaimer
Roivant Sciences Ltd. published this content on June 17, 2025, and is solely responsible for the information contained herein. Distributed via Public Technologies (PUBT), unedited and unaltered, on June 17, 2025 at 17:07 UTC.