Aurinia to Participate in H.C. Wainwright 26th Annual Global Investment Conference

On August 28, 2024 Aurinia Pharmaceuticals Inc. (NASDAQ: AUPH) (Aurinia or the Company) reported that the Company’s management team will attend the H.C. Wainwright 26th Annual Global Investment Conference in New York City, September 9-11, 2024 (Press release, Aurinia Pharmaceuticals, AUG 28, 2024, View Source [SID1234646147]).

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Aurinia management will host one-on-one meetings with investors and will participate in a fireside chat and Q&A session on Tuesday, September 10, at 10:30 AM EST. This session will not include a webcast.

Aprea Therapeutics to Present at the H.C. Wainwright Annual Global Investment Conference

On August 28, 2024 Aprea Therapeutics, Inc. (Nasdaq: APRE) ("Aprea" or the "Company"), a clinical stage biopharmaceutical company focused on precision oncology through synthetic lethality, reported that Oren Gilad Ph.D, President and Chief Executive Officer, will provide a corporate update at the H.C. Wainwright 26th Annual Global Investment Conference to take place September 9-11, 2024 in New York, NY (Press release, Aprea, AUG 28, 2024, View Source [SID1234646146]). Details are as follows:

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H.C. Wainwright 26th Annual Global Investment Conference

Date: September 9-11, 2024
Location: New York, NY
Webcast: click here

The above presentation is available to access "on-demand", beginning at 7:00 A.M. (ET), on September 9, 2024. It will be available for 90 days.

Management will be available for one-on-one meetings with institutional investors. To request a meeting, please contact your conference representative.

Alkermes to Participate in the Morgan Stanley 22nd Annual Global Healthcare Conference

On August 28, 2024 Alkermes plc (Nasdaq: ALKS) reported that management will participate in a fireside chat presentation at the Morgan Stanley 22nd Annual Global Healthcare Conference on Wednesday, Sept. 4, 2024 at 2:35 p.m. EDT (7:35 p.m. BST) (Press release, Alkermes, AUG 28, 2024, View Source [SID1234646144]). The live webcast may be accessed under the Investors tab on www.alkermes.com and will be archived for 14 days.

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TheraPPI announces publication of preclinical data in Nature Communications, demonstrating the inhibition of ERK/MyD88 interaction as a promising cancer treatment

On August 27, 2024 TheraPPI Bioscience SAS ("TheraPPI"), a preclinical biotechnology company focused on developing small molecules that modify protein interactions, reported the publication of extensive preclinical research in Nature Communications on small molecules that disrupt the ERK/MyD88 interaction (Press release, TheraPPI, AUG 27, 2024, View Source [SID1234657193]). These scientific findings stem from the work of scientists led by Isabelle Coste and Toufic Renno at the Lyon Cancer Research Center (CRCL), in collaboration with Stéphane Giraud at the Center for Drug Discovery and Development (CRCL, Synergy Lyon Cancer Foundation).

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"The publication of these results in Nature Communications provides crucial external validation from experts in ERK biology and the cancer field, enhancing visibility within the scientific community" commented Toufic Renno, Ph.D, team leader at the CRCL and CSO at TheraPPI. "Disrupting the ERK/MyD88 interaction directly kills cancer cells, as shown in multiple cancer models in mouse and patient-derived cells, while also triggering an anti-tumor immune response. Achieving this combined effect through a small molecule targeting RAS-MAPK pathway is a highly innovative breakthrough. This powerful discovery has the potential to significantly improve therapies for patients with advanced cancers."

"Current targeted therapies against RAS-MAPK pathway, primarily enzymatic inhibitors, are effective for treating cancer, but their efficacy is often short-lived and they typically fail to elicit an anti-tumor immune response" stated Luc Otten, MD, Ph.D., CEO of TheraPPI. "The data reported by TheraPPI’s scientific co-founders highlight the potential of inhibiting ERK/MyD88 interaction to revolutionize RAS-MAPK pathway targeting and demonstrate the scientific rationale for developing TheraPPI’s first programme, which focuses on targeting ERK/MyD88 to fight cancer and is currently in non-clinical development stage."

About the Publication:
"Targeting ERK-MYD88 interaction leads to ERK dysregulation and immunogenic cancer cell death" was published online in Nature Communications on August 15, 2024. The paper and its supplementary information are open access, and co-author disclosures are included within the paper.

Hansaitai Announces HX301 IND Approval from the National Medical Products Administration

On August 27, 2024 HanX Biopharmaceuticals reported that it has received approval from the National Medical Products Administration ( NMPA) for its HX301 clinical trial (Press release, HanX Biopharmaceuticals, AUG 27, 2024, View Source [SID1234655960]). This application meets the relevant drug registration requirements and authorizes Hans Ait Pharmaceuticals to conduct a clinical trial combining this product with temozolomide for glioblastoma.

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HX301 (Narazaciclib ) is a clinical-stage investigational small molecule multikinase inhibitor being jointly developed by Hans -Eti and international partners. Two Phase I clinical trials have been conducted and completed in the United States and China. Phase I monotherapy data demonstrated favorable safety and tolerability, supporting entry into Phase II and combination trials. The company currently plans to conduct multicenter Phase II trials in China and the United States for multiple clinical indications. Preclinical animal model studies have demonstrated that HX301 can cross the blood-brain barrier and exhibits monotherapy activity against glioblastoma, with enhanced activity when combined with temozolomide.

Dr. Lei Zhang, Chief Medical Officer of HansAiTec, said: "We are very pleased that HX301 has received clinical approval from the National Medical Products Administration. Despite various attempts in recent years, there have been no major breakthroughs in the field of glioblastoma, and many challenges still exist. Therefore, the development of new drugs has great potential. We look forward to rapidly advancing this clinical trial to provide patients with new treatment options to meet unmet medical needs."