Novavax And Commonwealth Of Australia Announce Agreement In Principle For Acquisition Of Novavax Covid-19 Vaccine
Novavax, Inc. (Nasdaq: Nvax), A Late Stage Biotechnology Company Developing Next-Generation Vaccines For Serious Infectious Diseases, Announced The Signing Of A Non-Binding Heads Of Terms Document With The Australian Government To Supply 40 Million Doses Of The Company&Rsquo;S Covid-19 Vaccine Candidate, Nvx-Cov2373, For The Australian Community."This Arrangement With The Australian Government Reflects The Importance Of The Ongoing Clinical Development Of Nvx-Cov2373, And Will Ensure That The Citizens Of Australia Will Have Access To Its Supply," Said Stanley C. Erck, President And Chief Executive Officer Of Novavax. "We Are Pleased With The Progress Of Our Ongoing Phase 3 Clinical Trial In The Uk, And Are Pressing Forward To Deliver Efficacy Data For Nvx-Cov2373, With Interim Data In This Event-Driven Trial Expected As Soon As Early First Quarter 2021."The Heads Of Terms Provides For The Delivery Of Nvx-Cov2373 To Australia Starting As Early As The First Half Of 2021, Subject To The Successful Completion Of Phase 3 Clinical Development And Approval Of The Vaccine By Australia&Rsquo;S Therapeutic Goods Administration (Tga). The Vaccine Regimen Is Expected To Require Two Doses Per Individual, Administered 21 Days Apart.To Date, Novavax Has Established Various Agreements For The Supply Of Nvx-Cov2373 Directly To The United States And The United Kingdom, Canada And Now Australia, And Through Partnerships, Supply To Japan, South Korea And India. Australia'S Clinical Trial ContributionAustralia Has Played A Pivotal Role In The Clinical Development Program For Nvx-Cov2373. Australian Clinical Researchers Led The Global Phase 1 Clinical Trial In August. This Trial Involved 131 Australians Across Two Trial Sites (Melbourne And Brisbane). In Addition, Approximately 690 Australians Have Participated In The Phase 2 Arm Of The Clinical Trial, Which Has Been Conducted Across Up To 40 Sites In Australia And The U.S.The Planned Global Phase 3 Clinical Programs Evaluating Nvx-Cov2373 Will Assess Immunity, Safety And Covid-19 Disease Prevention. The Trials Seek To Recruit Members Of The Community Most Vulnerable To Covid-19 - The Elderly, Those With Underlying Medical Conditions As Well As Diverse Racial And Ethnic Representation. About Nvx-Cov2373Nvx-Cov2373 Is A Vaccine Candidate Engineered From The Genetic Sequence Of Sars-Cov-2, The Virus That Causes Covid-19 Disease. Nvx-Cov2373 Was Created Using Novavax&Rsquo; Recombinant Nanoparticle Technology To Generate Antigen Derived From The Coronavirus Spike (S) Protein And Contains Novavax&Rsquo; Patented Saponin-Based Matrix-M&Trade; Adjuvant To Enhance The Immune Response And Stimulate High Levels Of Neutralizing Antibodies. Nvx-Cov2373 Contains Purified Protein Antigen And Cannot Replicate, Nor Can It Cause Covid-19. In Preclinical Trials, Nvx-Cov2373 Demonstrated Induction Of Antibodies That Block Binding Of Spike Protein To Receptors Targeted By The Virus, A Critical Aspect For Effective Vaccine Protection. In The Phase 1 Portion Of Its Phase 1/2 Clinical Trial, Nvx-Cov2373 Was Generally Well-Tolerated And Elicited Robust Antibody Responses Numerically Superior To That Seen In Human Convalescent Sera. Nvx-Cov2373 Is Also Being Evaluated In A Phase 3 Trial In The Uk And Two Ongoing Phase 2 Studies That Began In August; A Phase 2B Trial In South Africa, And A Phase 1/2 Continuation In The U.S. And Australia. Novavax Has Secured $2 Billion In Funding For Its Global Coronavirus Vaccine Program, Including Up To $388 Million In Funding From The Coalition For Epidemic Preparedness Innovations (Cepi). About Matrix-M&Trade;Novavax' Patented Saponin-Based Matrix-M&Trade; Adjuvant Has Demonstrated A Potent And Well-Tolerated Effect By Stimulating The Entry Of Antigen Presenting Cells Into The Injection Site And Enhancing Antigen Presentation In Local Lymph Nodes, Boosting Immune Response. About ManufacturingNovavax Is Progressing Large-Scale Manufacturing Of Nvx-Cov2373 Across Multiple Locations Around The World. Delivery Of Initial Doses Of The Vaccine Is Expected As Early As The End Of This Year, With The Goal To Expand The Production To Enable Delivery Of Over 2 Billion Doses Annually, Once All Production Is Online.

Optimize Your trial insights with Clival Database.
Are you exhausted from the uncertainty of trial insights pricing? Clival Database ensures the clarity in the midst of the global scenario for clinical trials to you.Clival Database is one of the best databases that offers an outstanding number of clinical trial data in terms of 50,000+ molecules and from primary regulatory markets as well as new entrants like Indian and Chinese markets.
With Clival, you get accurate positioning of historical sales data, patent database, company profiling, safety & efficacy, and prediction of launch of new innovative molecules helping you to align your research and driving down the cost.
To add value, we further break down our analytics for you so that improving your operational effectiveness; optimizing your clinical trials; and offering you accurate and high-quality data at lowest possible prices becomes possible.
Elevate your trial success rate with the cutting-edge insights from Clival database.
Check it out today and make more informed sourcing decisions! Learn More!