Monopar Initiates Clinical Trial of Novel uPAR-Targeted Radiopharmaceutical Therapy in Advanced Cancers
October 07 2024 - 8:00AM
Monopar Therapeutics Inc. (Nasdaq: MNPR), a clinical-stage
radiopharma company focused on developing innovative treatments for
cancer patients, today announced that the Phase 1a clinical trial
for its novel therapeutic radiopharmaceutical MNPR-101-Lu (MNPR-101
conjugated to lutetium-177) is now active and recruiting patients
with advanced cancers.
The Phase 1a trial is an open-label dose-escalation study of
MNPR-101-Lu in patients with solid tumors. The first clinical trial
site activated for the study is the Melbourne Theranostic
Innovation Centre (MTIC) in Australia. To help identify those
patients most likely to benefit from MNPR-101-Lu, the trial will
only be open to those participating in the ongoing MNPR-101-Zr
Phase 1 imaging and dosimetry clinical trial.
MNPR-101 is Monopar’s proprietary antibody that targets the
urokinase plasminogen activator receptor (uPAR), which is expressed
in numerous tumor types including pancreatic, breast, colorectal,
ovarian, and bladder. By selectively targeting uPAR, Monopar aims
to deliver a radiopharma therapy that kills cancer cells while
minimizing damage to healthy tissue. Both clinical (link) and
preclinical (link) data to date have demonstrated highly specific
and durable tumor uptake of MNPR-101-Zr (MNPR-101 conjugated to
zirconium-89).
“We are very encouraged by the recently released human clinical
data and preclinical efficacy results (link), and are thrilled to
be launching this therapeutic trial months ahead of our originally
planned schedule,” said Chandler Robinson, MD, Monopar’s Chief
Executive Officer.
“We believe this may be the world’s first uPAR-targeted
therapeutic radiopharma clinical trial,” commented Andrew
Cittadine, Monopar’s Chief Operating Officer. “Our goal is to light
up the tumors with MNPR-101-Zr and then treat them with
MNPR-101-Lu.”
Further information about the MNPR-101-Lu trial is available at
www.ClinicalTrials.gov under study identifier
NCT06617169. Details about the ongoing MNPR-101-Zr
Phase 1 imaging and dosimetry clinical trial are available at
www.ClinicalTrials.gov under study identifier
NCT06337084.
About Monopar Therapeutics Inc.
Monopar Therapeutics is a clinical-stage radiopharmaceutical
company focused on developing innovative treatments for cancer
patients, including Phase 1-stage MNPR-101-Zr for imaging advanced
cancers, Phase 1a-stage MNPR-101-Lu and late preclinical-stage
MNPR-101-Ac225 for the treatment of advanced cancers, as well as
early development-stage radiopharma programs against solid cancers.
For more information, visit: www.monopartx.com.
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. The words “may,”
“will,” “could,” “would,” “should,” “expect,” “plan,” “anticipate,”
“intend,” “believe,” “estimate,” “predict,” “project,” “potential,”
“continue,” “target” and similar expressions are intended to
identify forward-looking statements, although not all
forward-looking statements contain these identifying words.
Examples of these forward-looking statements include: that by
selectively targeting uPAR, Monopar aims to deliver a radiopharma
therapy that kills cancer cells while minimizing damage to healthy
tissue; that Monopar believes MNPR-101-Lu may be the world’s first
uPAR-targeted therapeutic radiopharma clinical trial; and that
Monopar’s goal is to light up the tumors with MNPR-101-Zr then
treat it with targeted MNPR-101-Lu. The forward-looking statements
involve risks and uncertainties including, but not limited to: that
Monopar may not recruit and enroll patients in its MNPR-101-Lu
therapeutic study; that the Phase 1 imaging and dosimetry clinical
trial in advanced cancer patients with MNPR-101-Zr may not yield
consistently satisfactory results; that future preclinical or
clinical data may not be as promising as the data to date; that
MNPR-101-Zr and/or MNPR-101-Lu may cause unexpected serious adverse
effects or fail to be effective against the cancer tumors in
humans; that Monopar may expend available funds sooner than
anticipated or require additional funding due to change in
circumstances or unanticipated events; and the significant general
risks and uncertainties surrounding the research, development,
regulatory approval, and commercialization of imaging agents and
therapeutics. Actual results may differ materially from those
expressed or implied by such forward-looking statements. Risks are
described more fully in Monopar's filings with 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. Monopar undertakes no obligation to update such statements to
reflect events that occur or circumstances that exist after the
date on which they were made. Any forward-looking statements
contained in this press release represent Monopar’s views only as
of the date hereof and should not be relied upon as representing
its views as of any subsequent date.
CONTACT:
Monopar Therapeutics Inc. Investor Relations
Karthik Radhakrishnan Chief Financial Officer
karthik@monopartx.com
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Twitter: @MonoparTx LinkedIn: Monopar Therapeutics
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