News Brief: BAT progresses COVID-19 candidate vaccine into Phase I human clinical trials

BAT’s US Bio-tech arm, Kentucky BioProcessing (KBP) today announced plans to commence a Phase I first-time-in-human study of its COVID-19 vaccine candidate following approval of its Investigational New Drug application by the U.S. Food and Drug Administration (FDA). Enrollment for the study is expected to begin shortly. Full press release, intended for use by the media only, available … Continued

Reynolds Completes 2020 PMTA Submissions with Vuse Alto E-Cigarette Applications

Grouped Alto applications are final FDA submission for deemed products, representing both Vuse and VELO portfolios Reynolds completes 2020 deemed product PMTA submissions for one of the broadest portfolios in the industry Reynolds has provided the FDA with more than 530,000 pages of scientific data for review as part of all PMTA applications submitted More … Continued

VELO Pouch Premarket Tobacco Applications Submitted to FDA for Review by Reynolds

VELO pouch is second group of PMTAs for VELO products, and completes current VELO brand PMTA submissions  WINSTON-SALEM, NC. September 1, 2020 – Reynolds American Inc. (“Reynolds”) announces today the submission of a group of Premarket Tobacco Product Applications (“PMTAs”) to the U.S. Food and Drug Administration (“FDA”) seeking orders authorizing the marketing of VELO pouches. … Continued

Reynolds Submits First VELO Dissolvable Nicotine Lozenge Premarket Tobacco Product Applications

FDA applications are a first for VELO’s dissolvable nicotine lozenges   WINSTON-SALEM, N.C. – August 24, 2020 – Reynolds American Inc. (“Reynolds”) announces today the submission of a group of Premarket Tobacco Product Applications (“PMTAs”) to the U.S. Food and Drug Administration (“FDA”) seeking orders authorizing the marketing of VELO dissolvable nicotine lozenges. A grant of … Continued

Reynolds Submits Second and Third Complete Premarket Tobacco Product Applications

Vuse Vibe and Vuse Ciro join Reynolds’ Prior Vuse Solo Submission to FDA   WINSTON-SALEM, N.C. – April 15, 2020 – Reynolds American (“Reynolds”) announced today that it has submitted two new Premarket Tobacco Product Applications (“PMTAs”) to the U.S. Food and Drug Administration (“FDA”). Reynolds is seeking marketing orders for their Vuse Vibe and Vuse … Continued

BAT Working on Potential COVID-19 Vaccine Through US Bio-tech Subsidiary

Potential vaccine in development for COVID-19 using new, fast-growing tobacco plant technology – pre-clinical testing under way Tobacco plants offer the potential for faster and safer vaccine development compared to conventional methods Potential to manufacture 1-3 million doses of vaccine per week   April 1, 2020: BAT’s US bio-tech subsidiary, Kentucky BioProcessing (KBP), is developing a potential vaccine … Continued