Regulatory News:
As part of its effort to develop innovative treatments for
people living with rare cancers, Sanofi has entered into an
exclusive licensing agreement with RadioMedix, Inc., a US
clinical-stage biotechnology company developing
radiopharmaceuticals for PET imaging and targeted alpha therapy
(TAT) against unmet medical needs in cancer, and Orano Med, a
French clinical-stage biotechnology company, subsidiary of the
Orano Group, developing lead-212 (212Pb) radioligand therapies
(RLTs) against cancer.
This collaboration between Sanofi, RadioMedix and Orano Med
focuses specifically on the late-stage project, AlphaMedixTM
(212Pb-DOTAMTATE), which currently is being evaluated for the
treatment of adult patients with unresectable or metastatic,
progressive somatostatin-receptor expressing neuroendocrine tumors
(NETs), a rare cancer. AlphaMedixTM is a TAT which consists of a
somatostatin receptor-targeting peptide complex radiolabeled with
lead-212 (212Pb) that serves as an in vivo generator of alpha
particles.
Dietmar Berger Chief Medical Officer,
Global Head of Development, Sanofi “We are excited to develop a
leading-edge project in the rapidly evolving field of radioligand
therapies in rare cancers. Early results for 212Pb have
demonstrated its differentiated biophysical and clinical profile,
reinforcing its potential to be a transformative radioligand
therapeutic for patients across multiple difficult-to-treat rare
cancers. This agreement underscores our efforts to explore
innovative collaborations that leverage novel technologies to
address the needs of people living with cancer.”
AlphaMedixTM has recently been granted Breakthrough Therapy
Designation in gastroenteropancreatic neuroendocrine tumors
(GEP-NETs) from the US Food and Drug Administration (FDA) for
patients who are naïve to peptide-receptor radionuclide therapy.
The FDA’s decision was based on findings from phase 1i and 2
clinical studies, which found that AlphaMedixTM was well tolerated
and provided substantial reduction in tumor burden, with a durable
response rate (ORR according to RECIST 1.1) of 62.5%.i AlphaMedixTM
is currently completing phase 2 clinical development, and the data
is being discussed with the FDA for potential regulatory filing and
approval.
Ebrahim S. Delpassand Chairman and
CEO, RadioMedix “The Breakthrough Therapy Designation of AlphaMedix
is a testament of its success in validating targeted alpha
therapies. We see this as a potential for the future of nuclear
oncology in general, and today it is pioneering next-generation
treatment for patients with neuroendocrine tumors. In our research,
we have seen that significantly higher energy delivery over much
shorter path lengths in the tissue of alpha emitters can overcome
the limitations of currently available beta emitter radioligand
therapies. We believe 212Pb is an ideal alpha emitter with highly
desirable physical and supply characteristics in comparison to
other alpha emitters. RadioMedix has been one of the pioneers in
the field of radioligand therapy in the U.S. and, through this
licensing agreement with Sanofi, our goal is to bring this
potentially life-saving therapy to as many patients as
possible.”
Julien Dodet President and CEO, Orano
Med “At Orano Med, we are at the forefront of innovation in
radioligand therapy and are developing a global industrial platform
for the manufacture and distribution of our 212Pb-conjugated drugs.
This marks a pivotal moment to expedite the development of this new
therapy and in our fight against cancer. Through this agreement, we
aim to lead the charge in advancing radioligand therapies with the
ambition to revolutionize cancer therapeutics.”
Under the licensing agreement, Sanofi will be responsible for
the global commercialization of AlphaMedixTM, while Orano Med will
be responsible for the manufacturing of AlphaMedixTM through its
global industrial platform currently under development. Under the
terms of the agreement, RadioMedix and Orano Med will receive an
upfront payment of €100 million and up to €220 million in sales
milestones and be eligible for tiered royalties. This agreement is
subject to standard regulatory approvals required for transactions
of this nature.
In striving to become the number one immunoscience company
globally, Sanofi remains committed to advancing oncology
innovation. Through focused strategic decisions the company has
reshaped and prioritized its pipeline, leveraging its expertise in
immunoscience to drive progress. Efforts are centered on
difficult-to-treat cancers such as select hematologic malignancies,
and solid tumors with critical unmet needs, including multiple
myeloma, acute myeloid leukemia, certain types of lymphomas, as
well as gastrointestinal and lung cancers.
About neuroendocrine tumors
Neuroendocrine tumors (NETs) are a heterogeneous group of rare
cancers that originate from neuroendocrine cells. These cancers
occur mostly in the gastrointestinal tract and pancreas but can
also occur in other tissues including the thymus, lung, and other
uncommon sites such as ovaries, heart, and prostate. Most NETs
strongly express somatostatin receptors. In the United States,
around 12,000 patients annually are expected to be diagnosed with
neuroendocrine tumors, with an average 5-year survival rate of 60%
at a metastatic stage. Despite the global prevalence of NETs
increasing each year, it is considered a rare cancer that is
estimated to affect approximately 35/100,000 individuals
worldwide.
About RadioMedix
RadioMedix, Inc. is a clinical-stage biotechnology company,
based in Houston and Humble, Texas. The company is focused on
innovative targeted radiopharmaceuticals for diagnosis, monitoring,
and therapy of cancer. RadioMedix is developing
radiopharmaceuticals for PET imaging and therapy (alpha- and
beta-labeled agents). The company established contract service
facilities for academic and industrial partners. including a cGMP
and analytical suite for Phase I-II-III clinical trials and
commercial launch. To learn more, visit www.radiomedix.com and
LinkedIn. For more information about this press release, please
contact: radiomedix@knbcomm.com.
About Orano Med
Orano Med, a subsidiary of the Orano Group, is a clinical-stage
biotechnology company that develops a new generation of targeted
therapies against cancer using the unique properties of lead-212
(212Pb), an alpha-emitting radioisotope and one of the more potent
therapeutic payloads against cancer cells known as Targeted
Alpha-Emitter Therapy (TAT). The company is developing several
treatments using 212Pb combined with various targeting agents.
Orano Med has 212Pb manufacturing facilities, laboratories, and
R&D centers in France and in the US and is currently investing
to further expand its GMP-manufacturing capacities for 212Pb
radiolabeled pharmaceuticals in North America and Europe.
As a recognized international operator in the field of nuclear
materials, Orano Group delivers solutions to address present and
future global energy and health challenges. Its expertise and
mastery of cutting-edge technologies enable Orano to offer its
customers high value-added products and services throughout the
entire fuel cycle. Every day, the Orano group’s 17,500 employees
draw on their skills, unwavering dedication to safety and constant
quest for innovation, with the commitment to develop know-how in
the transformation and control of nuclear materials, for the
climate and for a healthy and resource-efficient world, now and
tomorrow.
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 Forward-Looking Statements
This press release contains forward-looking statements as
defined in the Private Securities Litigation Reform Act of 1995, as
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trends in exchange rates and prevailing interest rates, volatile
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global crises may have on us, our customers, suppliers, vendors,
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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 with the exception of AlphaMedix.
i Delpassand ES, Tworowska I, Esfandiari R, et al. Targeted
α-Emitter Therapy with 212Pb-DOTAMTATE for the Treatment of
Metastatic SSTR-Expressing Neuroendocrine Tumors: First-in-Humans
Dose-Escalation Clinical Trial. J Nucl Med. 2022;63(9):1326-1333.
doi:10.2967/jnumed.121.263230.
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version on businesswire.com: https://www.businesswire.com/news/home/20240911369141/en/
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 Nicolas Obrist | + 33 6
77 21 27 55 | nicolas.obrist@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 More contact information available
here. RadioMedix radiomedix@knbcomm.com Orano Med Sophie
Letournel | +33 6 38 44 34 11 | sophie.letournel@orano.group
Orano Press Office | +33 (0)1 34 96 12 15 |
press@orano.group Investor relations Marc Quesnoy |
investors@orano.group
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