Fresenius Kabi prolongs the production and supply contract with Cerus Corporation for an additional 10 years

On May 3, 2022 Fresenius Kabi and the U.S. based company Cerus Corporation reported that it signed a new agreement for the production of systems for pathogen inactivation in blood components (Press release, Fresenius, MAY 3, 2022, View Source [SID1234613391]). The collaboration will help expanding access to pathogen-reduced blood components to patients. For many years, Cerus and Fresenius Kabi have collaborated regarding medical products specializing in pathogen inactivation for platelets and plasma. Since market launch of Cerus’ INTERCEPT systems, more than 11 million units have been in use worldwide.

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Lilly to Participate in Bank of America Securities 2022 Healthcare Conference

On May 3, 2022 Eli Lilly and Company (NYSE: LLY) reported that it will attend the Bank of America Securities 2022 Healthcare Conference, May 10-11, 2022 (Press release, Eli Lilly, MAY 3, 2022, View Source [SID1234613390]). Daniel Skovronsky, M.D., Ph.D., Lilly’s chief scientific and medical officer, and president of Lilly Research Laboratories, will participate in a fireside chat on Tuesday, May 10 at 7:40 p.m., Eastern time.

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A live audio webcast will be available on the "Webcasts & Presentations" section of Lilly’s Investor website at View Source A replay of the presentation will be available on this same website for approximately 90 days.

Curium’s Phase 3 ECLIPSE Trial Starts Enrolling Patients

On May 3, 2022 Curium reported it has successfully enrolled and dosed patients in the ECLIPSE Trial. ECLIPSE is a Phase 3, multi-center, open-label, randomized clinical trial comparing the safety and efficacy of 177Lu-PSMA-I&T versus standard of care hormone therapy in patients with metastatic castration-resistant prostate cancer (Press release, Curium, MAY 3, 2022, View Source [SID1234613389]). The clinical trial is enrolling patients at sites across the U.S. and will be opening clinical trial sites in Europe in 2022.

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"We are thrilled to see the ECLIPSE clinical trial progress with patients enrolled and treated with 177Lu-PSMA-I&T," said Renaud Dehareng, Curium’s Group CEO. "We are dedicated to redefining the experience of cancer through our trusted legacy in nuclear medicine. The ECLIPSE clinical trial demonstrates our commitment to patients with metastatic castration-resistant prostate cancer in North America and Europe."

"We would like to thank the investigators and healthcare providers at the clinical trial sites for their dedication to patients with metastatic castration-resistant prostate cancer," said Sakir Mutevelic, MD, Curium’s Chief Medical Officer. "Through our collaboration, we are working together to determine the safety and efficacy of this potential new investigational treatment for patients in need."

For more information about the ECLIPSE Trial, visit Curium’s Clinical Trial website or contact Curium’s Clinical Trial team directly at [email protected] with questions or to locate a clinical trial site near you.

CORMEDIX INC. TO REPORT FIRST QUARTER 2022 FINANCIAL RESULTS AND PROVIDE A CORPORATE UPDATE ON MAY 12

On May 3, 2022 CorMedix Inc. (Nasdaq: CRMD), a biopharmaceutical company focused on developing and commercializing therapeutic products for the prevention and treatment of infectious and inflammatory disease, reported that it will report its financial results for the first quarter ended March 31, 2022, after the market close on Thursday, May 12, 2022, and will host a corporate update conference call at 4:30pm Eastern Time (Press release, CorMedix, MAY 3, 2022, View Source [SID1234613388]).

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Cerus Corporation Announces New Manufacturing and Supply Agreement With Fresenius Kabi For INTERCEPT Blood System Sets

On May 3, 2022 Cerus Corporation (Nasdaq: CERS) reported that it has signed a ten-year agreement with Fresenius Kabi for the production of INTERCEPT Blood System sets (Press release, Cerus, MAY 3, 2022, View Source [SID1234613386]). This new contract replaces the current one with Fresenius Kabi that was set to expire in July 2025.

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"Our long-standing partnership with Fresenius Kabi has enabled us to ramp the adoption of our pathogen inactivation technology broadly around the globe, as we work to fulfill our mission of making the INTERCEPT Blood System the standard of care in transfusion medicine," said William ‘Obi’ Greenman, president and chief executive officer of Cerus. "After working together for more than 20 years, we are pleased to have extended our partnership commitment to meet the capacity requirements necessitated by the growth of our global business. This new cooperation secures numerous benefits for our companies, our customers and our shareholders, and it makes our supply chain more robust as we grow over the next decade."

Fresenius Kabi will continue producing sets for Cerus at its facility in La Châtre, France, and will also expand manufacturing operations to two new facilities, both located in the Caribbean. The addition of these sites will increase production volume for INTERCEPT Blood System sets and provide for the redundancy required for continuity of supply to Cerus’ large blood center and national transfusion service customers. Finally, with the expanded manufacturing footprint and increased production volumes, Cerus and Fresenius Kabi are focused on realizing additional economies of scale for both organizations.

"Cerus has been a valued partner, and we are excited to be announcing this next stage of our longstanding partnership with them today," stated Dr. Christian Hauer, Member of the Management Board Fresenius Kabi and President Fresenius Kabi MedTech. "With the INTERCEPT Blood System, Cerus offers a best-in-class pathogen reduction technology that many blood centers, hospitals, and patients across the globe rely on. We look forward to continuing to help Cerus transform the transfusion medicine field and improve blood safety and availability around the world with our high-quality products."

For over two decades, Cerus and Fresenius Kabi have collaborated to deliver pathogen inactivation for platelets and plasma around the globe, with cumulative doses of INTERCEPT blood components estimated to be in excess of 11 million since the products were first commercially launched.