Extensive updates from broad and innovative
portfolio also to be presented
- The 2023 American Academy of Dermatology (AAD) Annual Meeting
will see the data premiere of the phase III OLYMPIA 2 trial, where
nemolizumab monotherapy met all primary and key secondary endpoints
and demonstrated significant improvements on itch, skin clearance
and sleep disturbance in adult patients with prurigo nodularis
- Four additional posters explore the disease burden of prurigo
nodularis, a debilitating disease with limited treatment
options
- Twenty-one posters include updates on dermatologic conditions
such as sensitive skin, acne, and rosacea, as well as the latest
data from the aesthetics portfolio
- The company’s commitment to Diversity and Inclusion in
Dermatology has been featured through the sponsorship of activities
with the George Washington University School of Medicine and their
novel educational Dermatology Atlas
Galderma, the leading company solely dedicated to advancing the
future of dermatology, today premiered the positive phase III
results from the OLYMPIA 2 trial evaluating the efficacy, safety,
pharmacokinetics and immunogenicity of nemolizumab compared with
placebo in adult patients with prurigo nodularis. The results were
presented as a late-breaking presentation at the 2023 American
Academy of Dermatology (AAD) Annual Meeting by Dr. Shawn Kwatra,
Associate Professor of Dermatology at the Johns Hopkins University
School of Medicine. Galderma has an extensive presence at the
meeting with further updates from its broad portfolio across
Therapeutic Dermatology, Dermatological Skincare and Injectable
Aesthetics.
The phase III OLYMPIA 2 trial met all primary endpoints, showing
nemolizumab monotherapy significantly improved pruritus (itch) and
skin lesions compared with placebo in adult patients with moderate
to severe prurigo nodularis. Results showed that:
- 56 percent of nemolizumab-treated patients achieved a response
in itch intensity, as defined by an at least 4-point improvement in
peak-pruritus numerical rating scale (PP-NRS) score, compared to 21
percent in the placebo group (p<0.0001)
- 38 percent of nemolizumab-treated patients reached treatment
success in skin lesions, as defined by an investigator’s global
assessment (IGA) score of 0 or 1, compared to 11 percent in the
placebo group (p<0.0001)
Key secondary endpoints showed rapid onset of action and
significant improvements in itch and sleep disturbance
(p<0.0001) as early as week 4:
- Over five times as many patients in the nemolizumab group vs
placebo achieved significant and clinically meaningful improvement
in itch intensity, as defined by a 4-point improvement in PP-NRS -
(41.0% for nemolizumab vs 7.7% for placebo p<0.0001)
- Nearly four times as many patients in the nemolizumab group
versus placebo achieved significant and clinically meaningful
improvement in sleep disturbance as measured by a 4-point
improvement in sleep disturbance numerical rating scale (SD-NRS) -
(37.2% for nemolizumab vs 9.9% for placebo p<0.0001)
- The safety profile was consistent with the phase II trial
results
“OLYMPIA 2 is a key piece of the largest
phase III clinical development program ever undertaken in prurigo
nodularis to date. On behalf of my co-investigators worldwide, I am
honored and proud to present the study results to the scientific
community in a late-breaking presentation. The results confirm the
potential of this every four weeks injectable monoclonal antibody
targeting the IL-31 receptor alpha, with rapidly acting effects on
itch and sleep disturbance, and subsequent improvement of skin
lesions.”
SHAWN KWATRA, M.D. ASSOCIATE
PROFESSOR OF DERMATOLOGY JOHN HOPKINS UNIVERSITY
Further commitment to diversity in dermatology announced
Also at the congress, Galderma shared an exciting update on the
sponsorship of the Atlas initiative, in a highly anticipated booth
session focused on Diversity and Inclusion in Dermatology. The
unique educational session explored how to diagnose dermatologic
conditions in an array of skin tones, leveraging the renowned book
and online gallery ‘Full Spectrum of Dermatology: A Diverse and
Inclusive Atlas’, from the George Washington University School of
Medicine. The event took place on Friday, March 17 and was hosted
by editors of the Atlas, Dr. Adam Friedman and Dr. Misty Eleryan.
As part of the Galderma sponsorship, copies of the Atlas book are
being distributed throughout the AAD congress. Galderma is also
proud to be providing an additional financial grant to pilot a
pathway for other healthcare professionals to contribute to the
online gallery.
“We are so pleased that we’re able to bring
so much powerful new data to this year’s AAD congress. The data
premiere from OLYMPIA 2 confirms the potential that nemolizumab is
expected to improve outcomes for people with prurigo nodularis,
which can have such a profound impact on the lives of those
affected. Beyond this, our continued involvement and investment in
the Atlas program demonstrates our commitment to address every skin
need, with diversity and inclusion at the very heart of that
promise.”
BALDO SCASSELLATI SFORZOLINI, M.D.,
Ph.D. GLOBAL HEAD OF R&D GALDERMA
Extensive updates from Galderma’s broad and innovative
portfolio through posters and presentation sessions Galderma is
the only pure-play dermatology category leader, with more than 40
years of heritage in dermatology. Its continued commitment to
delivering science and innovation across a highly differentiated
portfolio is reflected in its extensive presence at AAD. More
details on Galderma’s scientific poster presentations can be found
here.
About the OLYMPIA 2 trial OLYMPIA 2 was a randomized,
double-blind, placebo-controlled phase III clinical trial, to
assess the efficacy and safety of nemolizumab monotherapy compared
with placebo in patients at least 18 years of age with prurigo
nodularis after a 16-week treatment period. The trial also assessed
pharmacokinetics and immunogenicity of nemolizumab compared to
placebo. OLYMPIA 2 included 274 patients with moderate-to-severe
prurigo nodularis.
About prurigo nodularis Prurigo nodularis is a
debilitating, chronic skin condition with thick skin nodules
covering large body areas and associated intense itch.1,2,3 Prurigo
nodularis affects an estimated 72 per 100,000 adults aged 18-64
years in the United States, primarily middle-aged women and
disproportionately people of African descent.1,4
About nemolizumab Nemolizumab is an investigational drug
and Galderma has not received approval for any indication in any
country. Nemolizumab is a first-in-class investigational monoclonal
antibody directed against the IL-31 receptor alpha that blocks
signaling from IL-31. IL-31 is a neuroimmune cytokine that is
recognized as driving multiple disease mechanisms in both prurigo
nodularis and atopic dermatitis. With its unique role in directly
stimulating sensory neurons related to itch and contributing to
inflammation and barrier dysfunction, IL-31 is the bridge between
the immune and nervous systems while also directly acting on
structural cells in the skin. Nemolizumab was granted Breakthrough
Therapy designation by the U.S. Food and Drug Administration (FDA)
in December 2019 for the treatment of pruritus associated with
prurigo nodularis, a status reconfirmed in February 2023.
About Galderma Galderma is the pure-play dermatology
category leader, present in approximately 90 countries. We deliver
an innovative, science-based portfolio of premium flagship brands
and services that span the full spectrum of the fast-growing
dermatology market through Injectable Aesthetics, Dermatological
Skincare and Therapeutic Dermatology. Since our foundation in 1981,
we have dedicated our focus and passion to the human body’s largest
organ – the skin – meeting individual consumer and patient needs
with superior outcomes in partnership with healthcare
professionals. Because we understand that the skin we’re in shapes
our lives, we are advancing dermatology for every skin story.
Galderma’s portfolio of flagship brands includes Restylane®,
Dysport®, Azzalure®, Alluzience® and Sculptra® in Injectable
Aesthetics; Soolantra®, Epiduo®, Differin®, Aklief®, Epsolay®,
Twyneo®, Oracea®, Metvix®, Benzac® and Loceryl® in Therapeutic
Dermatology; and Cetaphil® and Alastin® in Dermo-cosmetics. For
more information, visit www.galderma.com.
References:
1 Williams KA, Roh YS, Brown I, et al. Pathophysiology,
diagnosis, and pharmacological treatment of prurigo nodularis.
Expert Rev Clin Pharmacol. 2021;14(1):67-77.
doi:10.1080/17512433.2021.1852080 2 Elmariah S, Kim B, Berger T, et
al. Practical approaches for diagnosis and management of prurigo
nodularis: United States expert panel consensus. J Am Acad
Dermatol. 2021;84(3):747-760. doi:10.1016/j.jaad.2020.07.025 3
Whang KA, Mahadevan V, Bakhshi PR, et al. Prevalence of prurigo
nodularis in the United States. J Allergy Clin Immunol Pract.
2020;8(9):3240-3241. doi:10.1016/j.jaip.2020.05.051 4 Huang AH,
Canner JK, Khanna R, Kang S, Kwatra SG. Real-world prevalence of
prurigo nodularis and burden of associated diseases. J Invest
Dermatol. 2020;140(2):480-483.e4. doi:10.1016/j.jid.2019.07.697
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For further information:
Christian Marcoux, M.Sc. Chief Communications Officer
christian.marcoux@galderma.com +41 76 315 26 50
Rachel Mooney Global Franchise Communications
rachel.mooney@galderma.com +41 76 261 64 41
Zach Randles-Friedman Head of U.S. Communications
Zach.Randles-Friedman@galderma.com +1 305 299 5700