"I can't emphasise enough the complexity of maintaining an absolute temperature from the depot to the surgery," said Nick Jackson, head of programmes and innovative technologies at the Coalition for Epidemic Preparedness Innovations.
"It's incredibly difficult even on a good day with vaccines that are refrigerated. But the challenges are made harder as you begin to lower the temperature requirements."
According to research by logistics firm DHL and consultancy McKinsey, at least two thirds of the world's population are unlikely to have easy access to any jab that needs to be maintained at sub-zero temperatures.
Katja Busch, DHL's chief commercial officer, told the Telegraph that she is unaware of distributing a human vaccine globally at below -70C.
"It's doable with a special package and dry ice," she said. "But the biggest question is what happens at the final, final mile, once the package has been dropped off."
Donald Trump, the US President, recently intimated that he would try and shortcut regulatory hurdles to license products ahead of the US presidential election on November 3.
And Boris Johnson, the British Prime Minister, has hinted at a special fast-track licensing process.
But in an unprecedented move yesterday, nine leading vaccine developers - including Pfizer, Moderna, GlaxoSmithKline and AstraZeneca, manufacturers of the Oxford vaccine - promised not to seek government approval of any vaccine without extensive safety and effectiveness data.
"We believe this pledge will help ensure public confidence in the scientific and regulatory process," they said.
The Oxford, AstraZeneca trial has now been delayed while a safety issue is investigated.
Elsewhere, Chinese firm SinoVac reported that its vaccine appears to be safe in older people in mid-stage trials, although it generated a slightly weaker immune response compared with younger adults.