Proteo Biotech AG becomes tiakis Biotech AG

On September 1, 2022 tiakis Biotech AG (formerly Proteo Biotech AG) reported that it has renamed the Company from Proteo Biotech AG to tiakis Biotech AG (Press release, Proteo Biotech, SEP 1, 2022, View Source [SID1234639181]).

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In addition, the Company has launched a new website to provide for a more concise point of contact for its business and research partners.

Novartis appoints Fiona Marshall, Ph.D., President of the Novartis Institutes for BioMedical Research as Jay Bradner, M.D., steps down from the Executive Committee of Novartis

On September 1, 2022 Novartis reported that James (Jay) E. Bradner, M.D., will step down from the Executive Committee of Novartis (ECN), effective October 31st after seven years leading research at Novartis (Press release, Novartis, SEP 1, 2022, View Source [SID1234618875]). Fiona H. Marshall, Ph.D., currently Senior Vice President and Global Head of Discovery Sciences, Preclinical Development and Translational Medicine at MSD (Merck & Co., Inc in USA), has been appointed as President of the Novartis Institutes for BioMedical Research (NIBR), effective November 1st, 2022 reporting to Vas Narasimhan, M.D., CEO of Novartis. Dr. Marshall will become a member of the ECN.

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"Leading NIBR has been a privilege for which I will forever be grateful," Jay Bradner said. "I am so proud of the medicines we have imagined together, and I am confident that Fiona and our leaders will continue the creative, productive and important research to the definitive benefit of those with life-threatening diseases."

Vas Narasimhan said: "I am deeply grateful to Jay for his invaluable contributions to reimagining how we discover innovative medicines, recruiting world-class scientific leaders and expanding our collaborations with leading biotech companies and academic institutions. I wish him the very best in his future endeavors and am grateful Jay has agreed to assist with the transition."

"I am delighted to welcome Fiona to Novartis. She is both an esteemed biomedical scientist and an accomplished biopharmaceuticals research leader. Her three decades of experience leading drug discovery and early development across large biopharma, biotech and academia and her deep passion for biomedical science make her the ideal leader to help us strengthen our innovation pipeline and advance future waves of high-value medicines."

Fiona Marshall said: "I am very excited to join Novartis and lead the discovery teams who are renowned for their collaborative research and use of cutting-edge technologies. I look forward to working with them, colleagues across Novartis and our partners across the biopharma ecosystem to accelerate the translation of scientific discoveries into breakthrough medicines that address critical areas of unmet need for patients."

Prior to joining Merck in 2018, Dr. Marshall was a Founder and Chief Scientific Officer of Heptares Therapeutics, a successful UK Biotech company focused on structure-based drug design that was subsequently acquired by the Japanese biotech company Sosei, where she continued to serve as Chief Scientific Officer. Earlier in her career, Dr. Marshall was Director of Molecular Pharmacology at Millennium Pharmaceuticals and spent 10 years at GSK, holding senior positions in Molecular Pharmacology and Neuroscience. She holds a BSc in Biochemistry from University of Bath (UK) and Ph.D. in Neuroscience from University of Cambridge (UK). Dr. Marshall is the recipient of the 2012 WISE Women of Outstanding Achievement for Innovation and Entrepreneurship Award, and the 2015 RSC Malcolm Campbell Award for chemistry and the Vane Medal from the British Pharmacological Society. She is a Fellow of the Royal Society and the Academy of Medical Sciences, Honorary Fellow of the British Pharmacological Society and Honorary Fellow of the Royal Society of Chemistry.

Ascendis Pharma A/S Announces Upcoming Investor Presentations in September

On September 1, 2022 Ascendis Pharma A/S (Nasdaq: ASND) reported that the company is scheduled to participate in three upcoming investor conferences in September (Press release, Ascendis Pharma, SEP 1, 2022, View Source [SID1234618893]).

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Details:

Event Citi’s 17th Annual BioPharma Conference
Location Boston, MA
Date Wednesday, September 7, 2022
Time 3:30-4:15 p.m. Eastern Time / 12:30-1:15 p.m. Pacific Time
Speaker(s) Scott Smith, Senior Vice President, Chief Financial Officer

Event 2022 Wells Fargo Healthcare Conference
Location Boston, MA
Date Thursday, September 8, 2022
Time 8:35-9:05 a.m. Eastern Time / 5:35-6:05 a.m. Pacific Time
Speaker(s) Scott Smith, Senior Vice President, Chief Financial Officer

Event Morgan Stanley 20th Annual Global Healthcare Conference
Location New York, NY
Date Tuesday, September 13, 2022
Time 1:30-2:00 p.m. Eastern Time / 10:30-11:00 a.m. Pacific Time
Speaker(s) Jan Mikkelsen, President and Chief Executive Officer and Scott Smith, Senior Vice President, Chief Financial Officer
A live webcast of the events will be available on the Investors & News section of the Ascendis Pharma website at View Source A webcast replay will also be available on this website shortly after conclusion of each event for 30 days.

Halozyme to Participate in the 2022 Wells Fargo Healthcare Conference

On September 1, 2022 Halozyme Therapeutics, Inc. (NASDAQ: HALO) ("Halozyme") reported that Dr. Helen Torley, president and chief executive officer, is scheduled to present and host investor meetings at the 2022 Wells Fargo Healthcare Conference being held in Boston, MA on September 7-9, 2022 (Press release, Halozyme, SEP 1, 2022, View Source [SID1234618910]).

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A live audio webcast of the presentation will be available in the Investor Relations section of the Company’s website. Replays of the audio webcast will be available for 90 days following the conference.

High-Grade Glioma Relapse in Children: Onxeo announces the enrollment of the first patient in the phase 1b/2 clinical study conducted by the European ITCC consortium and sponsored by Institut Curie

On September 1, 2022 Onxeo S.A. (Euronext Growth: ALONX, Nasdaq First North[1]: ONXEO), a clinical-stage biotechnology company specializing in the development of innovative drugs targeting tumor DNA Damage Response (DDR)n in particular against rare or resistant forms of cancer, reported that the first patient has been enrolled and treated in the phase 1b/2 clinical study that aims to evaluate the efficacy and tolerability of AsiDNA[2], Onxeo’s first-in-class DDR inhibitor, combined with radiotherapy in children, adolescents or young adults with relapsed High-Grade Glioma (HGG) (Press release, Onxeo, SEP 1, 2022, View Source [SID1234618877]). The clinical validation of this innovative therapy offers the hope of providing better care and treatment for these high-risk pediatric cancers.

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High Grade Gliomas (HGG), which represents approximately 20% of tumors of the central nervous system (CNS) in children, continue to have a very poor prognosis with a 5-year survival rate of less than 20%. Surgery combined with radiotherapy or chemotherapy often allows the disease to be controlled. However, this disease control is not durable due to the development of treatment-resistant tumor cells. Studies conducted in preclinical models as well as initial clinical trials conducted in adults[3] have highlighted AsiDNA’s synergetic effect when combined with treatments that target and destroy the DNA, such as radiotherapy.

This phase 1b/2 trial, sponsored by Institut Curie, is being conducted within the framework of the European ITCC[4] consortium, in order to evaluate AsiDNA’s efficacy and tolerability by enrolling a maximum of 32 patients (children, adolescents or young adults) with relapsed HGG. A first patient has been enrolled in the study at the Institut Curie’s SIREDO (Soins, Innovation, Recherche en cancérologie de l’Enfant, l’aDOlescent et l’adulte jeune, i.e. care, innovation, research in cancer in children, adolescents and young adults) Center. Additionally, other French centers as well as European countries are planned to be initiated in the coming months. The study’s first interim results are projected in the first quarter of 2024.

Shefali Agarwal, Onxeo’s President and Chief Executive Officer, stated: "Onxeo is proud of its clinical collaboration with Institut Curie, and would like to thank Professor François Doz – the study’s lead investigator – for his involvement in this project. We hope that the combination of AsiDNA and radiotherapy in this type of cancer will provide a real benefit to patients suffering from a recurrent form of high-grade glioma".

"The enrollment of the first patient is a major step in this proof-of-concept study whose goal is to evaluate the efficacy and good tolerability of the systemic administration of AsiDNA in combination with a new radiotherapy. We hope that this study will provide encouraging evidence enabling an improvement in the prognostic outcome of a disease that is a key unmet need", added Prof. François Doz, pediatric oncologist, deputy head of clinical research, innovation and teaching at Institut Curie’s SIREDO Center and this study’s lead investigator.

This phase 1b/2 study is supported by a grant from the European Fight Kids Cancer[5] program.

[1] The company reminds shareholders that the delisting of Onxeo shares from the First North Growth market in Copenhagen has been approved and the last day of trading on this market will be November 8, 2022. The company will keep its primary listing on Euronext Growth Paris.

[2] In 2016, Onxeo acquired DNA Therapeutics, a spin-off of Institut Curie building on the innovative work of Marie Dutreix, CNRS research director research at Institut Curie, which led to the development of AsiDNA.

[3] "First-in-human phase I study of the DNA repair inhibitor DT01 in combination with radiotherapy in patients with skin metastases from melanoma." Le Tourneau C et al. Br J Cancer. 2016 May 24;114(11):1199-205.

[4] The Innovative Therapies for Children with Cancer (ITCC) consortium is a non-profit organization incorporating 63 European pediatric oncology departments with expertise in conducting early-stage trials in children and adolescents and 25 European research laboratories.

[5] Fight Kids Cancer is a European call for projects, a joint initiative of France’s Imagine for Margo association, Belgium’s KickCancer foundation and Luxembourg’s Kriibskrank Kanner foundation.