Allergan puts Vraylar on blockbuster track with new bipolar depression nod

Allergan headquarters
Credit Suisse analysts predict Allergan's Vraylar could hit $1.16 billion in sales by 2026. (Allergan)

Allergan, badly in need of good news, finally has some to share with investors.

On Tuesday, the FDA greenlighted the company’s antipsychotic med Vraylar to treat depression in adults with bipolar disorder. The OK makes the drug the first of its kind to treat the full spectrum of symptoms in bipolar I, one of four main types of the mood-shifting disease.

And that's an important distinction, influential doctors have told SVB Leerink's Marc Goodman. "Having a product with a label across all of bipolar manic, mixed, and depressive episodes could differentiate Vraylar from other antipsychotics, as it simplifies the treatment approach and no longer requires physicians to split hairs and try to define patients as one type of bipolar disorder episode versus another," he wrote in a note to clients. 

Watch the Free Webinar

Chemistry Through Biology: Translating Molecular Biology Technologies into Practical Processes for API Production

Learn about the key advances and critical hurdles in transforming emerging molecular biology technologies into practical applications with commercially viable processes.

RELATED: Allergan’s first push for Vraylar uses house of cards to symbolize manic side of bipolar disorder

The go-ahead comes on the back of three pivotal trials showing six weeks of Vraylar beat placebo at easing depression symptoms, as measured by the Montgomery Asberg Depression Rating scale.

While the FDA nod was “generally expected,” it’s “still important,” Credit Suisse analyst Vamil Divan wrote in his own note to clients. Allergan’s execs have said the label update could double Vraylar’s sales potential, taking the product well above the $487 million it recorded in 2018. Divan and his team, for their part, expect to see the drug rake in $1.16 billion in 2026.

And Allergan can certainly use a boost in the CNS department. The company recently reported a double phase 3 flop for closely watched candidate rapastinel in major depressive disorder.

RELATED: After investor attacks, Allergan's reviewing 'all options'—and this time it's urgent, CEO says

"We are deeply disappointed with these results, and they are a vivid reminder that drug development is extremely challenging, especially in mental health,” David Nicholson, Allergan’s R&D chief, said in a statement at the time.

That setback was one of many to hit the drugmaker over the last couple of years. Restasis patent woes, serious Botox competition and asset-sale struggles have sunk shares, prompting unrest from activist investors and pledges from management for urgent action.

Suggested Articles

Which rollouts might suffer most? Those that treat chronic diseases, require doctors to administer them or face current competition, analysts say.

Novartis and Incyte will put their blockbuster JAK inhibitor into phase 3 clinical trials as a possible treatment for COVID-19, the drugmakers said.

The Cannes Lions canceled its advertising creativity conference for 2020 after media reports that many large ad agencies planned to opt out.