Herantis Pharma to participate in Inderes Life Science evening

On December 7, 2022 Herantis Pharma Plc ("Herantis"), developing disease modifying therapies for Parkinson’s disease, reported that CEO, Antti Vuolanto will participate and give a company presentation at (Press release, Herantis Pharma, DEC 7, 2022, View Source,c3678469 [SID1234624873]):

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Inderes Life Science evening

Date: December 13, 2022

Location: Helsinki, Finland

For more information, please contact:

Julie Silber/Gabriela Urquilla

Tel: +46 (0)7 93 486 277/+46 (0)72-396 72 19

Email: [email protected]

Touchlight and Odimma Therapeutics Announce Clinical Material Supply Agreement to Develop Personalised Cancer Therapy Utilising Doggybone DNA

On December 7, 2022 Touchlight, a biotechnology company pioneering enzymatic DNA production to enable genetic medicines, reported a development and supply agreement with Odimma Therapeutics, a French biotech company focusing on personalised cancer immunotherapy (Press release, Touchlight Genetics, DEC 7, 2022, View Source [SID1234624862]).

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"The agreement between Odimma and Touchlight is an important step forward to secure Odimma’s clinical development. Not only is Touchlight’s technology producing genetic material with very favourable characteristics for a clinical use but also in a timeframe extremely adapted to a personalized immunotherapy in oncology. "

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The agreement focuses on the provision of clinical material for use in Odimma’s oncological neoantigen program. Through the deal, Odimma will gain access to Touchlight’s proprietary doggybone DNA (dbDNA) vector technology, providing them with a clinical supply of personalised dbDNA, to support and underpin the development of their candidate immunotherapy cancer treatment. The program is expected to start clinical enrolment in 2023.

Odimma’s approach of harnessing the ability of the patient’s own immune system to specifically recognize non-self-targets displayed by tumour cells represents a step change in the field of immune oncology and opens new avenues for the treatment of difficult to target tumours.

The development of the neoantigen products required for the therapy has faced unique challenges, including lead time to obtain GMP DNA and complex supply chains. Touchlight’s enzymatic production process, with its 5-day manufacturing process, will therefore strongly support Odimma in its program development. This will also allow Odimma’s clinical study to commence promptly for the benefit of patients.

Touchlight’s doggybone DNA is a minimal, linear, double stranded, covalently closed DNA vector which is produced through an enzymatic manufacturing process. It can accommodate genes of interest of more than 20kb and is linearly scalable, making it highly adaptable to support a range of genetic medicines and is ideal for the development of mRNA vaccines, therapeutics, gene therapies and beyond.

Karen Fallen, CEO, Touchlight commented: "We are delighted to be supporting Odimma on this ground-breaking program. Innovation in enzymatic DNA manufacturing is enabling advancements such as Odimma’s Immunotherapy program to deliver treatments to critically ill patients. With a rapid timeline to GMP and high-fidelity process, doggybone DNA is helping to overcome existing industry bottlenecks and the challenges associated with plasmid DNA."

Jean-Marc Limacher, MD, Chairman of Odimma Therapeutics said: "The agreement between Odimma and Touchlight is an important step forward to secure Odimma’s clinical development. Not only is Touchlight’s technology producing genetic material with very favourable characteristics for a clinical use but also in a timeframe extremely adapted to a personalized immunotherapy in oncology.

Enterome presents two posters on Phase 2 data of its lead immunotherapy, EO2401, in recurrent glioblastoma (ROSALIE study) at ESMO IO 2022

On December 7, 2022 Enterome, a clinical stage biopharmaceutical company developing first-in-class immunomodulatory drugs based on its gut bacterial Mimicry drug discovery platform, reported that it will present updated efficacy, immunogenicity and safety data from its Phase 2 trial of EO2401 in combination with nivolumab +/- bevacizumab, in patients with first progression/recurrence of glioblastoma (ROSALIE trial) in two poster presentations at the ESMO (Free ESMO Whitepaper) Immuno-Oncology Congress which is taking place in Geneva, Switzerland, December 7-9 2022 (Press release, Enterome, DEC 7, 2022, View Source [SID1234624857]).

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EO2401 is a first-in-class OncoMimics peptide-based immunotherapy able to rapidly activate and significantly expand existing effector memory CD8+ T cells against tumor-associated driver antigens due to their strong cross-reactivity with OncoMimics peptides.

Professor Wolfgang Wick, Universitätsklinikum and German Cancer Research Center, Heidelberg (Germany) will present the two posters on Thursday December 8th at the Poster Display Session ID 44 from 12:30 to 13:15 CET.

The poster details are as follows:

Poster Details – Abstract #170P
Title: EO2401 microbiome derived therapeutic vaccine + nivolumab +/- bevacizumab, in neoadjuvant, adjuvant and non-surgery linked treatment of recurrent glioblastoma: phase 1-2 EOGBM1-18/ROSALIE study
Authors: W. Wick et al.

Link to abstract can be accessed here.

Poster Details – Abstract #185P
Title: Interim analysis of the EOGBM1-18 study: Strong immune response to therapeutic vaccination with EO2401 microbiome derived therapeutic vaccine + nivolumab
Authors: W. Wick et al.

Link to abstract can be accessed here.

In addition, Enterome will present another poster on in vitro assays and in vivo evaluations in healthy donors demonstrating that OncoMimics peptides can elicit strong immune responses against tumors through cross-reaction of pre-existing, highly prevalent (>80% in the population) CD8+ T cells against targeted Tumor-Associated Antigens (TAAs).

Poster Details – Abstract #180P
Title: Recalling pre-existing microbiota-specific T cells to target tumors
Authors: J.-M. Carpier et al.

Link to abstract can be accessed here.

About EO2401
EO2401 is Enterome’s first-in-class off-the-shelf OncoMimics peptide-based immunotherapy. It combines three microbial-derived OncoMimics peptides that closely mimic specific cytotoxic T cell (CD8+ T cell) epitopes on the Tumor-Associated Antigens IL13Ra2, BIRC5 and FOXM1, combined with the helper peptide (CD4+ T cell epitope) Universal Cancer Peptide 2 (UCP2). EO2041 is designed to trigger the immune system into recognizing these epitopes on glioblastoma cells as foreign (non-self) and eliciting a targeted memory T-cell driven cell-killing response against the tumor cells.

About ROSALIE
ROSALIE (EOGBM1-18, NCT04116658) is a multicenter, open-label, Phase 1/2 trial investigating EO2401 in combination with nivolumab, and in combination with nivolumab/bevacizumab in patients with glioblastoma at first progression/recurrence after surgery and adjuvant radiotherapy/temozolomide. The trial is assessing safety, tolerability, immunogenicity and preliminary efficacy in more than 80 patients at centers in the US and Europe.

Calidi Biotherapeutics to Present at the 7th Annual Oncolytic Virotherapy Summit

On December 6, 2022 Calidi Biotherapeutics, Inc. (Calidi), a clinical-stage biotechnology company that is pioneering allogeneic cell-based platforms to revolutionize oncolytic virus therapies, reported an upcoming presentation at the 7th Annual Oncolytic Virotherapy Summit, taking place in Boston, Massachusetts and virtually, December 6-8, 2022 (Press release, Calidi Biotherapeutics, DEC 7, 2022, View Source [SID1234624831]).

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Details of the presentation are below:

Title: Allogeneic Stem Cell-Based Platforms to Potentiate and Deliver Oncolytic Virus Therapies
Date: Thursday December 8th, 2022, 10:00 a.m. ET
Presenter: Boris Minev M.D., President, Medical & Scientific Affairs, Calidi Biotherapeutics

Remedybio announces participation in INSPIRE and successful grant funding

On December 6, 2022 RemedyBio, a Dublin based biotech company, inspired by functional biology for the discovery and development of new immune therapies using the power of its Nanoreactor Technology for the analysis of individual cells and cell interactions, reported their participation in INSPIRE, a €12.8 million lung cancer program (Press release, Remedy Biologics, DEC 6, 2022, View Source [SID1234644158]). In one of the largest ever grants for preclinical research in lung cancer, RemedyBio will collaborate with programme leader, OmniSpirant and other European partners spanning across biotechnology, medical devices, cancer research, academia and patient advocacy.

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With the successful award of the grant by Horizon Europe, the INSPIRE consortium are already actively working on the program deliverables, and recently met in Galway, Ireland for the official kick off meeting. As well as OmniSpirant and RemedyBio, the consortium partners include Aerogen Limited (Ireland), Trinity College Dublin (Ireland), EVerZom (France), Biopharma Excellence (Pharmalex) (Germany), Deutsches Krebsforschungszentrum (DKFZ) (Germany) and Lung Cancer Europe (LuCE) (Switzerland).
Over the next 3 years, the INSPIRE programme aims to make an important and tangible impact on Europe’s Beating Cancer Plan and the EU Mission on Cancer. The consortium partners will work to develop a novel, effective and affordable lung cancer treatment via the development of a transformative new lower cost gene therapy. This project will place Europe as a leader in the fight against lung cancer and in the development of treatments for other debilitating lung diseases.
RemedyBio’s key role in the programme will be based on using RemedyBio’s proprietary Nanoreactor technology to investigate functional cell to cell interactions between the tumour and the gene therapy, building understanding of the efficacy of the new therapy.
"We are delighted to be part of the INSPIRE consortium in order to develop new and more effective therapies that impact patients lives", said Dan Crowley, CEO of Remedy Bio. "Our Nanoreactor technology and understanding of cell to cell interaction with help to drive insight and direction with our consortium partners in developing new RNA based therapeutics for lung cancer."