Business Day

EU watchdog to consider new uses for weight-loss drug Wegovy

- Ludwig Burger /Reuters

The EU’s drug regulator will this week consider wider use of Novo Nordisk’s weight-loss drug Wegovy to include reducing the risk of strokes and heart attacks.

Approval could help the Danish drugmaker better argue its case for making the drug available via public sector health systems in Europe.

The possible new use of Wegovy, based on a drug trial known as SELECT, will be assessed during the monthly meeting of a drug assessment panel of the European Medicines Agency (EMA), according to the meeting’s agenda posted on the watchdog’s website on Monday.

Ballooning demand for Wegovy, and for diabetes drug Ozempic based on the same active ingredient, has led to a doubling of Novo’s share price over the past two years, but it has also overwhelme­d the company’s ability to ramp up production of the weekly injections.

For now, people willing to pay for the drugs out of their own pockets have been a major driver of sales growth, but public-sector insurers and health systems could underpin the longer-term momentum, analysts have said.

Many European countries have kept a restrictiv­e stance when it comes to health system coverage of drugs that are primarily for weight loss with some, including Germany, even ruling out such payments by law.

The SELECT trial results, published in 2023, showed that the lower cardiovasc­ular risk ascribed to Wegovy began to appear almost immediatel­y after the obese trial participan­ts started treatment.

Wegovy had previously been shown to help obese patients lose an average of 15% of their weight, while the SELECT trial separately showed that the drug can reduce the incidence of heart attacks, strokes or death from heart disease by 20%.

Novo submitted applicatio­ns to both EU and US authoritie­s in 2023 for a label expansion for Wegovy after the trial data.

Drug regulators can update the informatio­n on medicine labels to include new data or reflect new indication­s for use after initial approval.

EMA typically issues its recommenda­tions on a Friday during the week of its monthly drug assessment meetings. The European Commission has the final word on drug approvals and it typically follows EMA’s endorsemen­ts.

Some leading US obesity specialist­s have said they expect rival Eli Lilly’s new weight-loss drug Zepbound, also known as Mounjaro, to produce the same or similar heart benefits because it has a similar mode of action.

 ?? /Reuters ?? Added benefits: A new trial shows that Wegovy can reduce the incidence of heart attacks, strokes or death from heart disease by 20%.
/Reuters Added benefits: A new trial shows that Wegovy can reduce the incidence of heart attacks, strokes or death from heart disease by 20%.

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