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Sanofi's rilzabrutinib earns orphan designation in the EU for IgG4-related disease Data from the positive Phase 2 study evaluating rilzabrutinib for the treatment of IgG4-related disease presented at EULAR

Key Takeaway: Sanofi's rilzabrutinib has been granted orphan designation by the European Medicines Agency for the treatment of IgG4-related disease. The approval follows positive results from a Phase 2 study presented at the EULAR 2025 Congress, showing reduced disease flare and maintenance of safety profiles. Rilzabrutinib also holds orphan designations for other conditions, including immune thrombocytopenia, and is under regulatory review in multiple regions. Its effective use for IgG4-RD may help address the urgent healthcare challenges posed by this rare disease.

Market Sentiment Analysis

POSITIVE FACTORS

  • Rilzabrutinib has earned orphan designation in the EU, indicating its potential value for treating rare diseases.
  • The Phase 2 study results show treatment with rilzabrutinib effectively reduces disease flare and gluco-corticoid use.
  • The safety profile of rilzabrutinib remains consistent with previous studies, showing no new safety concerns.

Full Press Release Details

Sanofi's rilzabrutinib earns orphan designation in the EU for IgG4-related disease
Paris, August 14, 2025. The European Medicines Agency has granted orphan designation to
rilzabrutinib, a reversible covalent Bruton's tyrosine kinase (BTK) inhibitor, for IgG4-related disease (IgG4-RD). EMA grants orphan designation to investigational therapies addressing rare,
life-threatening or debilitating medical diseases or conditions that affect no more than 5 in 10,000 persons in the EU.
Rilzabrutinib for the
treatment of IgG4-related disease was evaluated in a phase 2 study (clinical study identifier: NCT04520451) and results were presented
at the European Alliance of Associations for Rheumatology (EULAR) 2025 Congress. In IgG4-RD patients, treatment with rilzabrutinib for 52 weeks led to reduction in disease flare, other disease markers, and
glucocorticoid sparing. The safety profile of rilzabrutinib in the study was consistent with previous studies, with no new safety signals observed.
In addition to IgG4-related disease, rilzabrutinib has received orphan designations for immune thrombocytopenia (ITP) in the US, the EU, and Japan;
and for warm autoimmune hemolytic anemia, IgG4-RD and sickle cell disease in the US.
Rilzabrutinib has also been granted fast track designation in the US in ITP and IgG4-RD.
Rilzabrutinib is currently under regulatory review in the US, the EU, and China for its potential use in ITP. The target action date for the US FDA
regulatory decision for ITP, which was granted fast track designation, is August 29, 2025.
Rilzabrutinib is an investigational agent, and
its safety and efficacy have not been evaluated by any regulatory authority.
Rilzabrutinib is a novel, advanced, oral, reversible covalent BTK inhibitor that has the potential to be an effective new medicine for several rare
immune-mediated or inflammatory diseases by working to restore immune balance via multi-immune modulation. BTK, expressed in B cells, macrophages, and other innate immune cells, plays a critical role in multiple immune-mediated disease processes and
inflammatory pathways. With the application of the TAILORED COVALENCY technology, rilzabrutinib can selectively inhibit the BTK target while potentially reducing the risk of off-target side effects.
IgG4-RD is a progressive, relapsing, chronic immune-mediated rare disease, which can manifest
in almost every organ and can lead to organ damage and irreversible dysfunction with a sometimes-fatal outcome. People with IgG4-RD experience frequent flare-ups of the
condition characterized by periods of exacerbated symptoms. It affects approximately eight out of 100,000 adult patients in the US each year. Due to its rarity and challenges with diagnosis, the global prevalence of
Sanofi is an R&D driven, AI-powered biopharma company committed to improving people's lives and
delivering compelling growth. We apply our deep understanding of the immune system to
invent medicines and vaccines that treat and protect millions of people around the world, with an innovative pipeline that could benefit millions more. Our team is guided by one purpose: we
chase the miracles of science to improve people's lives; this inspires us to drive progress and deliver positive impact for our people and the communities we serve, by addressing the most urgent healthcare, environmental, and societal
challenges of our time.
Sanofi is listed on EURONEXT: SAN and NASDAQ: SNY
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Frequently Asked Questions

What is rilzabrutinib's designation in the EU?

Rilzabrutinib has received orphan designation for IgG4-related disease.

What was the key finding of the phase 2 study on rilzabrutinib?

The study showed rilzabrutinib reduced disease flare and markers in IgG4-RD patients.

What is the target action date for rilzabrutinib in the US?

The target action date for rilzabrutinib in the US is August 29, 2025.

How does rilzabrutinib work in the body?

It selectively inhibits Bruton's tyrosine kinase to restore immune balance.

What diseases is rilzabrutinib being evaluated for?

It is being evaluated for IgG4-RD and immune thrombocytopenia among others.

Last updated: Aug 14, 2025