Novartis presents Rhapsido® (remibrutinib) data at AAAAI, showing potential beyond chronic spontaneous urticaria (CSU)

Novartis presents Rhapsido® (remibrutinib) data at AAAAI, showing potential beyond chronic spontaneous urticaria (CSU)
arcticnovartis

  • Analyses from REMIX-1 & -2 studies on CSU disease control and early symptom relief will be presented
  • Phase II data evaluating safety and efficacy results of remibrutinib for treatment of peanut allergy to be featured in an oral session
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Novartis presents Rhapsido® (remibrutinib) data at AAAAI, showing potential beyond chronic spontaneous urticaria (CSU)

Novartis presents Rhapsido® (remibrutinib) data at AAAAI, showing potential beyond chronic spontaneous urticaria (CSU)
arcticnovartis

  • Analyses from REMIX-1 & -2 studies on CSU disease control and early symptom relief will be presented
  • Phase II data evaluating safety and efficacy results of remibrutinib for treatment of peanut allergy to be featured in an oral session
/by

Novartis presents Rhapsido® (remibrutinib) data at AAAAI, showing potential beyond chronic spontaneous urticaria (CSU)

Novartis presents Rhapsido® (remibrutinib) data at AAAAI, showing potential beyond chronic spontaneous urticaria (CSU)
arcticnovartis

  • Analyses from REMIX-1 & -2 studies on CSU disease control and early symptom relief will be presented
  • Phase II data evaluating safety and efficacy results of remibrutinib for treatment of peanut allergy to be featured in an oral session
/by

Novartis remibrutinib first therapy to achieve Phase III primary endpoint in chronic inducible urticaria (CIndU)

Novartis remibrutinib first therapy to achieve Phase III primary endpoint in chronic inducible urticaria (CIndU)
arcticnovartis

  • Statistically significant and clinically meaningful results seen in RemIND trial with complete responses achieved in 3 CIndU types1
  • Remibrutinib, a highly selective oral BTK inhibitor, was well-tolerated and demonstrated a favorable safety profile, including no liver safety concerns1
  • Oral remibrutinib has potential to be first targeted therapy approved for CIndU, which affects estimated 29 million adults worldwide2,3
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Novartis remibrutinib first therapy to achieve Phase III primary endpoint in chronic inducible urticaria (CIndU)

Novartis remibrutinib first therapy to achieve Phase III primary endpoint in chronic inducible urticaria (CIndU)
arcticnovartis

  • Statistically significant and clinically meaningful results seen in RemIND trial with complete responses achieved in 3 CIndU types1
  • Remibrutinib, a highly selective oral BTK inhibitor, was well-tolerated and demonstrated a favorable safety profile, including no liver safety concerns1
  • Oral remibrutinib has potential to be first targeted therapy approved for CIndU, which affects estimated 29 million adults worldwide2,3
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Novartis Vanrafia® Phase III data support slowing of kidney function decline in patients with IgA nephropathy

Novartis Vanrafia® Phase III data support slowing of kidney function decline in patients with IgA nephropathy
arcticnovartis

  • In ALIGN study, Vanrafia (atrasentan) showed positive difference in eGFR change from baseline vs. placebo at Week 136, 4 weeks after study treatment ended1
  • Results favored Vanrafia across multiple timepoints, measures of kidney function and in patients additionally receiving SGLT2 inhibitors1  
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Novartis Vanrafia® Phase III data support slowing of kidney function decline in patients with IgA nephropathy

Novartis Vanrafia® Phase III data support slowing of kidney function decline in patients with IgA nephropathy
arcticnovartis

  • In ALIGN study, Vanrafia (atrasentan) showed positive difference in eGFR change from baseline vs. placebo at Week 136, 4 weeks after study treatment ended1
  • Results favored Vanrafia across multiple timepoints, measures of kidney function and in patients additionally receiving SGLT2 inhibitors1  
/by

Novartis Vanrafia® Phase III data support slowing of kidney function decline in patients with IgA nephropathy

Novartis Vanrafia® Phase III data support slowing of kidney function decline in patients with IgA nephropathy
arcticnovartis

  • In ALIGN study, Vanrafia (atrasentan) showed positive difference in eGFR change from baseline vs. placebo at Week 136, 4 weeks after study treatment ended1
  • Results favored Vanrafia across multiple timepoints, measures of kidney function and in patients additionally receiving SGLT2 inhibitors1  
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Victor Bulto and Thierry Diagana named to 2026 TIME100 Health List

Victor Bulto and Thierry Diagana named to 2026 TIME100 Health List
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