Influence of COVID-19 on trust in routine immunization, health information sources and pandemic preparedness in 23 countries in 2023

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pediatrics associates of dallas :: Article Creator Pediatric Diagnostic Associates Will Continue Serving Families As A Practice Independent Of CHI Memorial Pediatric Diagnostic Associates, which was previously associated with CHI Memorial Hospital, announced Thursday it will again become an independent practice under newly formed Scenic City Pediatrics PLLC. Effective Feb. 1, the medical group will enter a new contract with BlueCross BlueShield of Tennessee, including Networks P and S, among other insurers, according to a news release. The change follows a June decision on BlueCross BlueShield of Tennessee's behalf to terminate its contract with Memorial relating to its Network S customers. Managing Partner Dr. Tony Friddell said in a phone interview Pediatric Diagnostic Associates has been under the CHI Memorial umbrella as a managed practice within the hospital system for 28 years. In some shape or form, Pediatric Diagnostic Associates...
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€7.34m for cancer vaccine developer - European Biotechnology

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Having secured a €2.785m grant from the EU and €4.55m from a Series B round, MaxiVAX is going full steam ahead with its Phase II cancer vaccine programmes.

Private clinical-stage biotech MaxiVAX announced that it has been awarded a European Commission grant of €2,785,000, thanks to the Horizon 2020 EIC Accelerator Programme. In addition, the company successfully closed a Series B2 round of CHF5m (€4.55m). Founded by the father and son team Bernard and Nicholas Mach, the Geneva-based biotech is focused on developing personalized anti-cancer vaccination.

MaxiVAX will use the funds to support the clinical development programmes which include the multi-centric efficacy Phase II trial for advanced, refractory head and neck cancers that is currently ongoing in Switzerland. The company will also start preparations for an international Phase II clinical study in a yet to be disclosed rare cancer indication, for which the FDA accepted the Investigational New Drug application in July 2018. The new funds will also be used to scale up production of the company’s lead compound, MVX-ONCO-1. MVX-ONCO-1 is the first personalised cell-based cancer immunotherapy using encapsulation cell technology. Therapy is individualised and can be applied to any cancer type.

“This important and welcome funding now enables us to move forward and accelerate our clinical programmes in Switzerland, Europe and the US,” commented MaxiVAX CEo Dimitrios Goundis. “We are encouraged by the progress in our ongoing Head & Neck Phase 2 trial, and look forward to its completion in 2021.”



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