Canadian biotechnology company Medicago said on 10 November 2020 that a combination of its experimental COVID-19 vaccine and GlaxoSmithKline's vaccine booster, produced virus-neutralising antibodies in all healthy volunteers in an early-stage study, Reuters news agency reported on Tuesday.
Medicago, which is backed by Mitsubishi Tanabe Pharma and tobacco giant Philip Morris, said it planned to move into mid-to-late-stage trials with a lower dose version of its vaccine, along with the GSK adjuvant.
The CEO of Medicago, Bruce Clark, told Reuters: "What we're most encouraged with is that we are able to go with the lowest dose for our phase 2/3 trials."
Reportedly, trials from rival COVID-19 vaccine developers have generally shown that lower doses produce less side effects.
However, Medicago did not disclose full safety data, but said side effects were mainly mild to moderate.
Medicago had signed its first vaccine supply agreement in October 2020 with Canada for up to 76 million doses.
Clark added the company was in talks with several other countries for potential deals.
GSK grants USD2m to boost adult vaccination efforts
Valneva and LimmaTech begin Phase 2 infant trial for Shigella vaccine candidate S4V2
Circio Holding and Entos Pharmaceuticals collaborate on circular RNA delivery
AKAGERA Medicines completes first cohort in phase 1 SAD/MAD study of AKG-100
Alzinova AB reports positive final Phase 1b results for ALZ-101 in Alzheimer's
Primrose Bio launches Prima RNApols ExTend RNA polymerase for long-template mRNA manufacturing
Merck's CAPVAXIVE approved by EC for pneumococcal disease prevention
Sanofi secures FDA fast track designation for chlamydia vaccine candidate
Anixa Biosciences secures US patent allowance for ovarian cancer vaccine
Valneva to supply IXCHIQ vaccine for chikungunya outbreak in La Réunion
Everest Medicines' EVM14 IND application receives US FDA approval
Clover Biopharmaceuticals' SCB-1019 IND application receives US FDA approval
Centivax partners with Emery Pharma on universal flu vaccine
Avance Biosciences registers with CLIA program
GSK receives approval from US FDA for Penmenvy 5-in-1 meningitis vaccine