Caladrius Biosciences Treats First Patient in the Phase 1b Trial of CLBS201 for the Treatment of Diabetic Kidney Disease
12 Abril 2022 - 7:00AM
Caladrius Biosciences, Inc. (Nasdaq: CLBS) (“Caladrius” or the
“Company”), a clinical-stage biopharmaceutical company
dedicated to the development of innovative therapies designed to
treat or reverse disease, today announced that the first patient
has been treated in its Phase 1b open-label, proof-of-concept study
of CLBS201 for the treatment of diabetic kidney disease (“DKD”) at
the Clinical Advancement Center in San Antonio, Texas. CLBS201 is
an investigational autologous CD34+ cell therapy product for
administration directly into the renal artery(ies) to reverse or
slow the decline of renal function in diabetic patients with
rapidly progressive chronic kidney disease (“CKD”).
“With this trial, we hope to bring much improved
patient outcomes to diabetic patients with reduced kidney function.
Specifically, we are targeting patients with later stage CKD. Based
on a wealth of published preclinical and early clinical data, we
believe that the innate ability of CD34+ cells to promote the
growth of new microvasculature could be a means to attenuate the
progression or, potentially, reverse the course of DKD,” said David
J. Mazzo, PhD, President and Chief Executive Officer of Caladrius.
“The treatment of the first patient in this Phase 1b study of
CLBS201 is another important milestone for our Company and we
anticipate top-line data by the first quarter of 2023.”
“Regenerative medicine is a new, but rapidly
evolving strategy for treating diabetic kidney disease and shows
much promise as a potential breakthrough,” stated Dr. Pablo
Pergola, Research Director, Renal Associates, P.A. , San Antonio,
Texas, and principal investigator for the study. “My practice is
proud and excited to be at the forefront of this effort.”
For more information on this study, please visit
clinicaltrials.gov (identifier: NCT04990427).
About Diabetic Kidney Disease
DKD, also called diabetic nephropathy, is a serious
kidney-related complication of diabetes. Diabetes mellitus is the
leading cause of kidney disease; approximately 40% of individuals
with diabetes have DKD.1 Over time, high blood sugar from poorly
controlled diabetes can damage the small blood vessels
(microvasculature) in the kidneys, which can lead to kidney damage.
This microvascular complication may eventually develop in
approximately 30% of patients with type 1 diabetes and
approximately 40% of patients with type 2 diabetes. All-cause
mortality in patients with DKD is reported to be higher than in
patients with diabetes without kidney
disease.2,3_______________________[1] Radica Z. Alicic, et al.
(2017) Diabetic Kidney Disease. CJASN, 12 (12) 2032-2045[2] Maltese
G, et al. (2015) Preventing diabetic renal disease: the potential
reno-protective effects of SGLT2 inhibitors. Br J Diabetes Vasc.
Dis. 15:114-118[3] Karalliedde J, et al. (2010) Proteinuria in
diabetes: bystander or pathway to cardiorenal disease? JASN.
21:2020-2027
About Caladrius Biosciences
Caladrius Biosciences, Inc. is a clinical-stage
biopharmaceutical company dedicated to the development of
innovative therapies designed to treat or reverse disease. We
currently are developing first-in-class autologous cell therapy
products based on the finely tuned mechanisms for self-repair that
exist in the human body. Our technology leverages and enables these
mechanisms in the form of specific cells, using formulations and
modes of delivery unique to each medical indication.
The Company’s current product candidates include:
XOWNA® (CLBS16), the subject of both a recently completed positive
Phase 2a study and an ongoing Phase 2b study
(www.freedom-trial.com) in the U.S. for the treatment of coronary
microvascular dysfunction (“CMD”); CLBS12 (HONEDRA® in Japan),
recipient of a SAKIGAKE designation in Japan and eligible for early
conditional approval for the treatment of critical limb ischemia
(“CLI”) and Buerger’s disease based on the results of an ongoing
clinical trial; and CLBS201, designed to assess the safety and
efficacy of CD34+ cell therapy as a treatment for diabetic kidney
disease (“DKD”). For more information on the Company, please visit
www.caladrius.com.
Safe Harbor for Forward-Looking
Statements
This press release contains forward-looking
statements within the meaning of the Private Securities Litigation
Reform Act of 1995. Forward-looking statements reflect management’s
current expectations, as of the date of this press release, and
involve certain risks and uncertainties. All statements other than
statements of historical fact contained in this press release are
forward-looking statements including, without limitation, any
expectations of revenues, expenses, cash flows, earnings or losses
from operations, cash required to maintain current and planned
operations, capital or other financial items; any statements of the
plans, strategies and objectives of management for future
operations; market and other conditions; any plans or expectations
with respect to product research, development and
commercialization, including regulatory approvals; any plans or
expectations to complete strategic transactions to diversify the
Company’s pipeline of development product candidates; any other
statements of expectations, plans, intentions or beliefs; and any
statements of assumptions underlying any of the foregoing. Without
limiting the foregoing, the words “plan,” “project,” “forecast,”
“outlook,” “intend,” “may,” “will,” “expect,” “likely,” “believe,”
“could,” “anticipate,” “estimate,” “continue” or similar
expressions or other variations or comparable terminology are
intended to identify such forward-looking statements, although some
forward-looking statements are expressed differently. Factors that
could cause future results to differ materially from the recent
results or those projected in forward-looking statements include
the “Risk Factors” described in the Company’s Annual Report on Form
10-K filed with the Securities and Exchange Commission (“SEC”) on
March 22, 2022, and in the Company’s other periodic filings with
the SEC. The Company’s further development is highly dependent on,
among other things, future medical and research developments, and
market acceptance, which are outside of its control. You are
cautioned not to place undue reliance on forward-looking
statements, which speak only as of the date of this Press Release.
Caladrius does not intend, and disclaims any obligation, to update
or revise any forward-looking information contained in this Press
Release or with respect to the matters described herein, except as
required by law.
Contact:
Investors:Caladrius Biosciences, Inc.John
MendittoVice President, Investor Relations and Corporate
CommunicationsPhone: 908-842-0084Email: jmenditto@caladrius.com
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