Cara Therapeutics Announces Oral KORSUVA™ (difelikefalin) Improves Itch and Inflammatory Biomarkers in Atopic Dermatitis Patients with Moderate-To-Severe Pruritus
March 28 2022 - 7:00AM
Cara Therapeutics, Inc. (Nasdaq: CARA), an early
commercial-stage biopharmaceutical company leading a new treatment
paradigm to improve the lives of patients suffering from pruritus,
today announced data from a sub-study of the KARE Phase 2 clinical
trial demonstrated Oral KORSUVA™ (difelikefalin) improved itch and
inflammatory biomarkers in atopic dermatitis (AD) patients with
moderate-to-severe pruritus. The biomarker data were presented
during the Late-Breaking Research: Clinical Trials session at the
2022 American Academy of Dermatology (AAD) Annual Meeting.
The sub-study, which included 40 patients from
the KARE trial, characterized the effect of Oral KORSUVA
(difelikefalin) on pruritus- and AD-related gene expression using
baseline and week 12 skin biopsies. Data pooled from all Oral
KORSUVA (difelikefalin) treatment groups indicated treatment with
Oral KORSUVA (difelikefalin) altered expression of multiple
individual pruritus- and AD-related genes. Gene set variation
analysis confirmed downregulation of pruritus-related genes and the
Th2 pathway following 12 weeks of treatment with Oral KORSUVA
(difelikefalin), but not placebo.
“Pruritus is extremely burdensome for patients
with atopic dermatitis and new treatment options that effectively
address pruritus and alleviate the itch-scratch cycle are greatly
needed,” said lead investigator Emma Guttman-Yassky, MD, PhD,
Waldman Professor and System Chair of Dermatology and Immunology at
the Icahn School of Medicine at Mount Sinai. “Results from our
sub-study demonstrate oral difelikefalin downregulated the
expression of key markers associated with pruritus and atopic
dermatitis inflammation, indicating the potential of difelikefalin
to provide an additional anti-inflammatory benefit in patients with
atopic dermatitis-related pruritus.”
In addition to the late-breaking oral
presentation, quality of life data from a subgroup analysis of the
KARE trial were presented in a poster at the 2022 AAD Annual
Meeting. The poster, “Oral Difelikefalin Improves Itch and Quality
of Life in Subjects With Itch-Dominant Atopic Dermatitis: Subgroup
Analysis of a Randomized, Phase 2 Study,” (#33993) is available at:
https://eposters.aad.org/.
About Cara Therapeutics
Cara Therapeutics is an early commercial-stage
biopharmaceutical company leading a new treatment paradigm to
improve the lives of patients suffering from pruritus. The
Company’s novel KORSUVA™ (difelikefalin) injection is the first and
only FDA-approved treatment for moderate-to-severe pruritus
associated with chronic kidney disease in adults undergoing
hemodialysis. The Company is developing an oral formulation of
difelikefalin and has initiated Phase 3 programs for the treatment
of pruritus in patients with non-dialysis dependent advanced
chronic kidney disease and atopic dermatitis. Phase 2 trials of
Oral KORSUVA (difelikefalin) are ongoing in primary biliary
cholangitis and notalgia paresthetica patients with
moderate-to-severe pruritus. For more information, visit
www.CaraTherapeutics.com and follow the company on Twitter,
LinkedIn and Instagram.
Forward-looking Statements
Statements contained in this press release regarding matters
that are not historical facts are "forward-looking statements"
within the meaning of the Private Securities Litigation Reform Act
of 1995. Examples of these forward-looking statements include
statements concerning Oral KORSUVA’s potential to provide a
benefit, including an anti-inflammatory benefit, to patients
suffering from atopic dermatitis-associated pruritus. Because such
statements are subject to risks and uncertainties, actual results
may differ materially from those expressed or implied by such
forward-looking statements. Risks are described more fully in Cara
Therapeutics’ filings with the Securities and Exchange Commission,
including the "Risk Factors" section of Cara Therapeutics’ Annual
Report on Form 10-K for the year ended December 31, 2021 and its
other documents subsequently filed with or furnished to the
Securities and Exchange Commission. All forward-looking statements
contained in this press release speak only as of the date on which
they were made. Except to the extent required by law, Cara
Therapeutics undertakes no obligation to update such statements to
reflect events that occur or circumstances that exist after the
date on which they were made.
MEDIA CONTACT:Annie Spinetta6
Degrees973-768-2170aspinetta@6degreespr.com
INVESTOR CONTACT:Iris Francesconi, Ph.D.Cara
Therapeutics203-406-3700investor@caratherapeutics.com
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