Tonix strives for pandemic readiness with new US manufacturing facility
The company's goal is to design and test new vaccines for novel pathogens within 100 days of a potential pandemic threat
Vaccines for monkeypox, smallpox and COVID-19 are among some of the products that will be developed by Tonix Pharmaceuticals at its new clinical-scale manufacturing facility in North Dartmouth, Massachusetts.
The clinical-stage biopharma company officially launched its Advanced Development Center (ADC) with a ribbon cutting ceremony on Tuesday. Tonix plans to develop vaccines against infectious diseases at the new facility using its recombinant pox virus platform technology, which it says is ‘rapidly deployable for addressing potential novel or emerging pathogens.’
The 45,000 sq ft facility features single-use bioreactors and purification suites with equipment for GMP production of vaccines for clinical trials, including the capability to produce sterile vaccines in glass bottles. It has been designated a Biosafety Level 2 site, a Centers for Disease Control and Prevention label which means the microbes there pose moderate hazards to laboratorians and the environment.
According to Tonix Pharmaceuticals CEO Seth Lederman, the facility will accelerate development of vaccines targeting infectious diseases.
He commented: ‘The ADC greatly enhances our ability to progress our pipeline of vaccines for infectious diseases, including monkeypox, smallpox and COVID-19. We believe that the recombinant pox virus platform technology underlying our key vaccines in development, TNX-801, TNX-1840 and TNX-1850, coupled with our capabilities at the Tonix R&D Center (RDC) for research and development, will be rapidly deployable for addressing potential novel or emerging pathogens, with simplified distribution and administration, relative to modified mRNA-based vaccines.’
Lederman said the company’s goal is to ‘be able to design and test new recombinant pox virus vaccines against novel pathogens within the 100 days of recognition of a potential emerging pandemic threat’, noting that this timeline meets criteria set out by the White House Office of Science and Technology Policy.
Tonix’s portfolio features a range of investigational new drugs or biologics that are progressing through clinical trials. These include TNX-102 SL, a candidate in mid-Phase 3 development for the management of fibromyalgia, and TNX-102 SL, which is being developed to treat Long COVID.
Related News
-
News Swiss pharma industry warns US tariffs could harm global patient care
The Swiss pharmaceutical sector has raised alarms over new US tariffs on medicines, warning of disrupted supply chains, increased costs, and delayed innovation, all of which could jeopardise patient access to essential treatments worldwide.
-
News Women in Pharma: CPHI India – India’s Pharmaceutical Industry and Gender Inclusion Challenges
India’s pharmaceutical industry has emerged as a significant player in the global market, valued at USD 50 billion in FY 2023-2024, according to Frost & Sullivan’s analysis. This sector encompasses a diverse portfolio, including drugs, vacc... -
News Biogen acquires Apellis Pharmaceuticals to boost immunology and rare disease profile
Biogen Inc. has announced its acquisition of Apellis Pharmaceuticals, Inc., a move that is set to significantly enhance its growth portfolio in immunology and rare diseases. The agreement, valued at approximately US$5.6 billion, will see Biogen purchas... -
News Gilead Sciences acquires Ouro Medicines for over US$2 billion
Gilead Sciences confirms a deal to take over Ouro Medicines, adding to a portfolio of therapies for autoimmune diseases.
-
News Women in Pharma: Advancing Women's Health
Discover the latest innovations in technologies and therapeutics that are revolutionising women's health in our latest CPHI Online Women in Pharma infographic.
-
News CPHI Pharma Awards 2026: Recognising Excellence in an Evolving Industry
Submissions now open — deadline May 16
-
News Dr Reddy's to launch generic semaglutide in India
Dr Reddy’s Laboratories, one of India’s leading pharmaceutical companies, is preparing to launch a generic version of semaglutide, branded as Obeda, in March. Obeda is expected to provide a more affordable alternative to Ozempic a... -
News Frontier Biotech and GSK Forge RNA Therapy Partnership
Frontier Biotechnologies and GSK have entered a global licensing agreement to advance small interfering RNA (siRNA) therapeutics. This collaboration grants GSK exclusive rights to develop and commercialise two promising siRNA candidates, marking a mile...