GSK’s Pivotal Test for mRNA Flu Vaccine Aims to Show Two Targets Are Better Than One - MedCity News
GSK is preparing to start a Phase 3 trial for its mRNA flu vaccine, which targets both HA and NA proteins. Phase 2 results showed robust immune responses in adults. The vaccine was acquired from CureVac in 2024 for €400 million. Moderna's mRNA flu vaccine, mFLUSIVA, was approved by the FDA in August 2024.
How this was made
The 30-second read
Why it matters
The Phase 3 initiation marks the first major clinical milestone for a next‑gen flu vaccine, potentially expanding GSK's vaccine portfolio.
Market read
Investors will watch trial outcomes for valuation impact on GSK and the broader vaccine sector.
What to watch
Regulatory timelines and manufacturing scale‑up costs could temper upside.
Background
GSK acquired CureVac's mRNA flu assets in 2024 and is now advancing a dual‑target HA/NA vaccine.
Ticker impact
GSK announced the start of a Phase 3 trial for its mRNA seasonal flu vaccine, a first‑in‑class pivotal study.
Potential upside if Phase 3 confirms efficacy; downside risk if trial fails.
The trial is the first major step after Phase 2; market will price in expectations of a differentiated product versus existing flu shots.
Market effects
Could boost the broader biotech/ vaccine sector if successful, prompting re‑rating of flu‑vaccine peers.
UK and European pharma markets may see modest uplift.
Sets a competitive benchmark against Moderna's HA‑only flu mRNA vaccine.
Counterpoint
If the trial fails, GSK may face a costly setback and lose momentum to competitors.
Key entities
- companyGSK
British pharmaceutical giant developing the mRNA flu vaccine.
- companyCureVac
Original developer of the mRNA flu candidates, now owned by BioNTech.



