Media Update: EADV: New data reinforce Sanofi’s innovative approach and leadership across immune-mediated skin diseases

25 septembre 2024
Télécharger le PDF

Partagez

EADV: New data reinforce Sanofi’s innovative approach and leadership across immune-mediated skin diseases

  • 24 abstracts for Dupixent, including 4 oral presentations, highlight impact of targeting interleukin-4 (IL4) and interleukin-13 (IL13) across atopic dermatitis (AD), prurigo nodularis (PN) and chronic spontaneous urticaria (CSU)
  • New data show impact of Dupixent on potential for clinical remission in children as young as six years of age with moderate-to-severe AD
  • 15 abstracts for immunology pipeline molecules, including phase 2 presentations in AD for amlitelimab, an OX40-ligand monoclonal antibody
     

Paris, September 25, 2024. Sanofi will present 39 abstracts across approved and pipeline medicines at the 2024 European Academy of Dermatology and Venereology (EADV) medical meeting from September 25-28 in Amsterdam, the Netherlands. Presentations will include 21 abstracts for Dupixent (dupilumab) in partnership with Regeneron, highlighting the impact of targeting IL4 and IL13 across three chronic skin conditions, including disease remission data and long-term data in children with moderate-to-severe atopic dermatitis (AD), and rapid results in adults with prurigo nodularis (PN). In addition, data presentations from Sanofi’s extensive immunology pipeline include oral and poster presentations for amlitelimab, an OX40-ligand monoclonal antibody, demonstrating safety and efficacy results in moderate-to-severe AD, as well as in poster presentations for rilzabrutinib, a novel oral BTK inhibitor, showing its impact on symptoms of AD and moderate-to-severe chronic spontaneous urticaria (CSU).

Dietmar Berger, M.D., Ph.D. 
Chief Medical Officer, Global Head of Development at Sanofi 
“Our data at EADV highlight the breadth of our diverse and novel approach across inflammatory dermatologic conditions, including AD, PN and CSU. Dupixent data demonstrates the potential benefit of important treatment goals such as clinical remission and the speed and durability of efficacy. We continue to evaluate Dupixent’s real-world safety profile and consistency of patient impact and satisfaction in children, adolescents, and adults with atopic dermatitis across the globe. Additionally, we are excited to share new data from our pipeline, including results for amlitelimab showing the potential to provide durable efficacy that may enable a quarterly dosing interval, with favorable safety profile.”

Notable presentations include:

Dupixent

New results and analyses for Dupixent in children and adults with moderate-to-severe AD and adults with prurigo nodularis.

Atopic dermatitis

  • multiple poster presentations will show results in children with moderate-to-severe AD, including those from an open-label extension study on clinical remission in children aged six to 17 years of age, including after stopping treatment with Dupixent, as well as long-term efficacy and safety data for up to two years on children aged six months to five years. Additionally, real-world data in children six months to 11 years of age will show patient-reported disease severity and health-related quality of life outcomes throughout one year.
  • an oral presentation will show real-world safety data from around the world for Dupixent in adults and adolescents with moderate-to-severe AD.

Prurigo nodularis

  • PRIME and PRIME2: an oral presentation will show new analyses on disease activity, itch, and skin clearance as early as two weeks from two pivotal clinical studies.
     

The safety results of these studies were generally consistent with the known safety profile of Dupixent in its approved dermatological indications.

Dermatology pipeline

Data include new results and analyses for amlitelimab, an OX40-ligand monoclonal antibody, in AD, and rilzabrutinib, a novel oral BTK inhibitor, in AD and CSU.

Atopic dermatitis

  • amlitelimab: six presentations will share data for amlitelimab in moderate-to-severe AD, including an oral presentation of 68-week safety results. Additional presentations highlight a PK model that support the potential use of a quarterly dosing regimen, a post-hoc analysis showing the impact of amlitelimab on AD of the head and neck, and results from an in vitro analysis demonstrating that the anti-OX40L mechanism of amlitelimab does not deplete T cells.
     
  • rilzabrutinib: a poster presentation will show the impact of rilzabrutinib on itch in adults with moderate-to-severe AD. 
     

Chronic spontaneous urticaria

  • rilzabrutinib: three poster presentations will show the impact of rilzabrutinib on itch, hives and urticaria in adults with moderate-to-severe CSU.
     

Hidradenitis suppurativa

  • three poster presentations will show the impact of disease symptoms on patients with hidradenitis suppurativa and highlight the need for increased disease awareness and effective treatment options.
     

Alopecia areata

  • a poster presentation will show conceptual model and clinical outcome measures in alopecia areata based on the patient experience.
     

Amlitelimab and rilzabrutinib are investigational medicines for which safety and efficacy have not been evaluated by any regulatory authority.

Complete list of EADV 2024 presentations:

Presenting authorAbstract titlePresentation details
Atopic dermatitis
DodgeCharacterization Of Atopic Dermatitis Medication Use Before and During Pregnancy in The United States (dupilumab)P0710 and FC08

Oral and e-Poster

Friday, September 27

4:40-4:50 CEST
IrvineGrowth Analysis in Children Aged 6 to 11 Years with Severe Atopic Dermatitis and Impact of 16 Weeks of Dupilumab Treatment on HeightLate Breaking News Number: 8073

Thursday, September 26

4:45-5:00 CEST
TzellosComprehensive Safety Data in Adult and Adolescent Patients With Atopic Dermatitis Treated With Dupilumab: Real-World Insights 1 Year Into the GLOBOSTAD Multinational Prospective Observational Study (dupilumab)P0452 and EPS05

Oral and e-Poster

Thursday, September 26

2:25-2:35 CEST
BaselgaDupilumab improves disease severity in children <12 years of age with severe atopic dermatitis: interim results from PEDISTAD Real-World Registry (dupilumab)P0666

e-Poster
BeckImpact of Dupilumab Treatment on Seasonal Disease Severity in Adults with Moderate-to-Severe Atopic Dermatitis (dupilumab)P0672

e-Poster
CorkDupilumab Treatment Restores Skin Barrier in Children Aged 6 to 11 Years with Moderate-to-Severe Atopic Dermatitis (dupilumab)P0710

e-Poster
GuyotDupilumab Demonstrates Higher Likelihood of Achieving Improvements in Signs, Symptoms and Quality of Life vs Lebrikizumab at Week 16: Results from a Placebo-adjusted Indirect Comparison AnalysisP0635

e-Poster
GuyotDupilumab Demonstrates Higher Likelihood of Maintaining Efficacy Outcomes Compared with Lebrikizumab in Monotherapy at Week 52: Results from a Placebo-adjusted Indirect Comparison AnalysisP0702

e-Poster
IrvineDupilumab Increases Levels of Bone Alkaline Phosphatase Irrespective of Prior Systemic Corticosteroids Use in Children with Moderate-To-Severe Atopic Dermatitis (dupilumab)P0728

e-Poster
KimLower Total IgE After Dupilumab Treatment is Associated with a Reduction in Flares in Patients with Moderate-to-Severe Atopic Dermatitis (dupilumab)P0667

e-Poster
PallerThe Effect of Atopic Dermatitis on The Height, Weight and BMI of Children Aged Up To 12 Years (dupilumab)P0665

e-Poster
PallerDupilumab Efficacy and Safety Up To 2 Years in Children Aged 6 Months To 5 Years with Atopic Dermatitis (dupilumab)P0725

e-Poster
SiegfriedTo Define Remission On- And Off-Drug and To Show That Sustained Remission Can Be Achieved with Dupilumab Treatment in Pediatric Patients with Moderate-To-Severe AD (dupilumab)P0655

e-Poster
SiegfriedDupilumab Treatment Provides Long-Term Improvement in Sleep Loss and Disease Control Over 1 Year in Pediatric Patients with Moderate-to-Severe Atopic Dermatitis (dupilumab)P0729

e-Poster
SimpsonDupilumab Improved Quality of Life in Patients with Localized Atopic Hand Dermatitis (dupilumab)P0699

e-Poster
StänderMaintenance of Itch Response in Adult Patients with Moderate-To-Severe Atopic Dermatitis Treated with Dupilumab: Post-Hoc Analysis from LIBERTY AD SOLO-CONTINUE (dupilumab)P0708

e-Poster
StroberSustained Improvement in Atopic Dermatitis Disease Control and Treatment Satisfaction with Dupilumab in Clinical Practice: 5-Year Follow-up Results From the RELIEVE-AD Study (dupilumab)P0704

e-Poster
StroberDupilumab Improves Patient-Reported Symptom Control Among Adults with Moderate-to-Severe Atopic Dermatitis in Clinical Practice: 5-Year Follow-Up Results From the RELIEVE-AD Study (dupilumab)P0702

e-Poster
BieberPrediction of the efficacy of extended dosing of amlitelimab (an anti-OX40 Ligand antibody) in patients with moderate-to-severe atopic dermatitis using a modeling approach (amlitelimab)P0687
e-Poster
Krueger In vitro evidence demonstrating the nondepleting mechanism of action of amlitelimab, an OX40 Ligand monoclonal antibody (amlitelimab)P0548 
e-Poster
Kwatra Amlitelimab (an anti-OX40 Ligand antibody) normalises the atopic dermatitis gene signature in the skin of patients with moderate-to-severe atopic dermatitis (amlitelimab)P0542 
e-Poster
Reich Impact of amlitelimab (an anti-OX40 Ligand antibody) on atopic dermatitis of the head and neck: post hoc results from the STREAM-AD phase 2b study of moderate-to-severe atopic dermatitis (amlitelimab)P0685 
e-Poster
Stein Gold Amlitelimab (an anti-OX40 Ligand antibody) vs placebo in patients with moderate-to-severe atopic dermatitis: Study design of phase 3 OCEANA clinical trials COAST 1/2, SHORE, AQUA, and ESTUARY [Encore] (amlitelimab)P0549 
e-Poster
Weidinger 68-week safety results of amlitelimab (an anti-OX40 Ligand antibody) in participants with moderate-to-severe atopic dermatitis from STREAM-AD Phase 2b dose-ranging and withdrawal study (amlitelimab)3310 and FC08
Oral Presentation
Friday, September 27  
4:00-4:10 PM CEST 
Magdalena Attributes of treatment and factors influencing patient preference and satisfaction in Atopic Dermatitis: Literature review (led by HVT) (disease awareness)P0531 
e-Poster
Guttman-Yassky Rilzabrutinib improves itch in atopic dermatitis (rilzabrutinib)P0709  
e-Poster
Prurigo nodularis
StänderDupilumab Provides Rapid and Continuous Improvement in Prurigo Nodularis Signs and Symptoms Over Time: Results From PRIME/PRIME2 (dupilumab)P2434 and EPS05

Oral and e-Poster

Thursday, September 26

2:15-2:25 CEST
JachieDupilumab in Adult Patients with Moderate-to-severe Prurigo Nodularis: 6-months Real-world Follow-up Results from the French Early Access Program (dupilumab)P3056

e-Poster
KimSequence of Improvement of Signs, Symptoms, and Quality of Life in Patients with Prurigo Nodularis Receiving Dupilumab (dupilumab)P2598

e-Poster
KimDupilumab Is Efficacious in Patients with Prurigo Nodularis Regardless of History of Atopic Comorbidities: Pooled Results from Two Phase 3 Trials (LIBERTY-PN PRIME and PRIME2) (dupilumab)P3076

e-Poster
Chronic spontaneous urticaria
MaurerResults From Two Phase 3 Studies of Dupilumab in CSU (dupilumab)P3585

e-Poster
MaurerDupilumab Reduces Disease Activity in Patients with Chronic Spontaneous Urticaria: LIBERTY-CSU CUPID Study A (dupilumab)P3593

e-Poster
Ben-Shoshan A 12-Week Safety Assessment of Rilzabrutinib in Patients With Chronic Spontaneous Urticaria From the RILECSU Phase 2 Dose-Ranging Study [Encore] (rilzabrutinib)P3614 
e-Poster
Giménez-Arnau Leveraging machine learning to develop a prognostic model for chronic spontaneous urticaria (rilzabrutinib)P3602 
e-Poster
Maurer Rilzabrutinib reduces biomarkers related to itch and disease severity in chronic spontaneous urticaria and atopic dermatitis (rilzabrutinib)P3069 
e-Poster
Hidradenitis suppurativa  
Agnes Patient experience of hidradenitis suppurativa: Ranking the burden of symptoms and impacts (led by HVT) (disease awareness)P0114 
e-Poster
Agnes Patient experience of pain in hidradenitis suppurativa: qualitative research on location, burden, impacts and management (led by HVT) (disease awareness)P0115 
e-Poster
Lucy Hidradenitis suppurativa community online across 7 countries converges on the need for disease awareness and effective treatment (led by HVT) (disease awareness)P0116 
e-Poster
Alopecia areata
Favaro Marcelo Patient experience in Alopecia Areata: Conceptual model and review of clinical outcome measures (led by HVT) (disease awareness)P2071 
e-Poster

About Sanofi
We are an innovative global healthcare company, driven by one purpose: we chase the miracles of science to improve people’s lives. Our team, across the world, is dedicated to transforming the practice of medicine by working to turn the impossible into the possible. We provide potentially life-changing treatment options and life-saving vaccine protection to millions of people globally, while putting sustainability and social responsibility at the center of our ambitions.
Sanofi is listed on EURONEXT: SAN and NASDAQ: SNY

Sanofi Media Relations
Sandrine Guendoul | + 33 6 25 09 14 25 | sandrine.guendoul@sanofi.com
Evan Berland | + 1 215 432 0234 | evan.berland@sanofi.com
Victor Rouault | + 33 6 70 93 71 40 | victor.rouault@sanofi.com
Timothy Gilbert | + 1 516 521 2929 | timothy.gilbert@sanofi.com

Sanofi Investor Relations
Thomas Kudsk Larsen |+ 44 7545 513 693 | thomas.larsen@sanofi.com
Alizé Kaisserian | + 33 6 47 04 12 11 | alize.kaisserian@sanofi.com
Arnaud Delépine | + 33 6 73 69 36 93 |arnaud.delepine@sanofi.com
Felix Lauscher | + 1 908 612 7239 | felix.lauscher@sanofi.com
Keita Browne | + 1 781 249 1766 | keita.browne@sanofi.com
Nathalie Pham | + 33 7 85 93 30 17 | nathalie.pham@sanofi.com
Tarik Elgoutni | + 1 617 710 3587 | tarik.elgoutni@sanofi.com
Thibaud Châtelet | + 33 6 80 80 89 90 | thibaud.chatelet@sanofi.com

Sanofi Forward-Looking Statements
This media update contains forward-looking statements as defined in the Private Securities Litigation Reform Act of 1995, as amended. Forward-looking statements are statements that are not historical facts. These statements include projections and estimates regarding the marketing and other potential of the product, or regarding potential future revenues from the product. Forward-looking statements are generally identified by the words “expects”, “anticipates”, “believes”, “intends”, “estimates”, “plans” and similar expressions. Although Sanofi’s management believes that the expectations reflected in such forward-looking statements are reasonable, investors are cautioned that forward-looking information and statements are subject to various risks and uncertainties, many of which are difficult to predict and generally beyond the control of Sanofi, that could cause actual results and developments to differ materially from those expressed in, or implied or projected by, the forward-looking information and statements. These risks and uncertainties include among other things, unexpected regulatory actions or delays, or government regulation generally, that could affect the availability or commercial potential of the product, the fact that product may not be commercially successful, the uncertainties inherent in research and development, including future clinical data and analysis of existing clinical data relating to the product, including post marketing, unexpected safety, quality or manufacturing issues, competition in general, risks associated with intellectual property and any related future litigation and the ultimate outcome of such litigation, and volatile economic and market conditions, and the impact that pandemics or other global crises may have on us, our customers, suppliers, vendors, and other business partners, and the financial condition of any one of them, as well as on our employees and on the global economy as a whole. The risks and uncertainties also include the uncertainties discussed or identified in the public filings with the SEC and the AMF made by Sanofi, including those listed under “Risk Factors” and “Cautionary Statement Regarding Forward-Looking Statements” in Sanofi’s annual report on Form 20-F for the year ended December 31, 2023. Other than as required by applicable law, Sanofi does not undertake any obligation to update or revise any forward-looking information or statements.

All trademarks mentioned in this press release are the property of the Sanofi group.

Attachment

 

Partagez