Sector News

Argenx straddles the line between drug promotion and awareness in latest unbranded DTC TV ad

March 5, 2022
Life sciences

Argenx has decided to do something a little different with its new unbranded DTC ad for myasthenia gravis (MG). The TV ad does not spend much time talking about the disease itself but largely points out that a new med is now available for patients, though the drug is never never mentioned directly.

There are typically two types of pharma ads: One is upfront and branded, talking about a company’s drug, its name, what it does and who it’s for. Then there are unbranded ads, which are focused more on raising awareness about diseases for which drugs are sold.

Argenx’s unbranded ad does not call out its recently approved drug, Vyvgart, by name but leans heavily on a drug promotion approach. The ad is titled simply “New Treatment Option,” and the 30-second spot shows several patients talking about why they want a new therapy—mainly because they want a normal life to work, to see friends, to get out of the house and to smile in family photos.

MG, which can cause severe muscle weakness, can stop patients from doing all of that. The narrator says “a new FDA-approved treatment for adults with [MG] could help them do more of the daily activities they care about.” It then directs the viewer to a link, NOW4MG.com, which takes you directly to a Vyvgart branded landing page.

When asked about this strategy, Rebecca McLeod, argenx’ U.S. general manager and marketing lead, said: “What we’ve heard from the patient population over the past few years is that [there] hasn’t been much forward innovation in treatments for them, and very little done in awareness.”

In terms of raising awareness about the disease, McLeod said argenx’s focus has largely been on talking to doctors and drilling down into Vyvgart’s new mechanism of action. Argenx has live sales reps out in the field despite COVID, though the pandemic is making this “difficult,” McLeod said.

“We’re also, partly because of COVID, focusing on non-personal promotion as well and trying to get through the clutter and finding a mix of meeting in-person or virtually and even deciding where [healthcare professionals] want to be met.” Some people want reps coming into the office, but others are more willing to connect if it’s not in person, and McLeod said they are looking to be pragmatic in their approach to cater for that.

In addition, in the run-up to the FDA approval two months ago for carcinogen fears—argenx’s first ever commercial product—the biopharma spent several years boosting awareness of MG. Vyvgart nabbed FDA approval Dec. 17, 2021.

Argenx’s disease awareness strategy included light-up nights around the country back in 2020 swiftly followed by a patient website debut and then a docuseries about the autoimmune disorder. In 2021, it turned to celebrity chef Sean Brock to debut an online cookbook with recipes for people with MG, who can have difficulty chewing and swallowing.

TV ads are not always the best way to get the attention of rare patients. Alnylam, which markets three RNAi drugs for rare diseases, this week told Fierce Pharma Marketing that for its newest drug Givlaari, it was deliberately not taking the DTC route because only around 5,000 patients in the U.S. and Europe have acute hepatic porphyria, the condition its drug is approved to treat.

But for argenx, the 65,000-patient number hits a sweet spot for DTCs to be worth the money. “We made a very deliberate decision out of the gate to go with an unbranded campaign to raise awareness of the disease itself,” explained McLeod.

Another focus of its overall marketing strategy is to show that Vyvgart is differentiated from AstraZeneca’s Soliris, its main competitor in the MG space. Soliris is a monoclonal antibody that targets complement protein C5, while Vyvgart is an antibody fragment that binds to the neonatal Fc receptor (FcRn), preventing FcRn from recycling immunoglobulin G back into the blood.

The biopharma may in the future have two more competitors in UCB and Johnson & Johnson, which both have late-stage MG assets, and UCB is nearing an FDA filing. For its part, J&J just this week set up an early marketing push in MG.

But argenx isn’t looking over its shoulder at what its competitors are doing. McLeod said it’s still “very early days” in terms of launch, having only been on the market for eight weeks, but that argenx is “cautiously optimistic” and “looking for a gradual uptake” of the drug.

By Ben Adams

Source: fiercepharma.com

comments closed

Related News

January 29, 2023

Colorcon, Inc. signs Put agreement with intent to acquire controlled atmosphere packaging specialist Airnov Healthcare Packaging

Life sciences

Airnov provides critical healthcare industries with high-quality, controlled atmosphere packaging, to protect their products from moisture and oxygen. The business has manufacturing facilities in the USA, France, China and India and employs around 700 people.

January 29, 2023

Takeda pledges up to $1.13B for rights to Hutchmed’s cancer drug fruquintinib outside of China

Life sciences

Takeda of Japan has partnered with Hong Kong-based Hutchmed, gaining the commercial rights to colorectal cancer drug fruquintinib outside of China for $400 million up front, plus $730 million in potential milestone payments. Takeda also will help develop fruquintinib, which can be applied to subtypes of refractory metastatic colorectal cancer, regardless of biomarker status, the companies said.

January 29, 2023

Vir taps Bayer dealmaker Marianne De Backer as its next CEO

Life sciences

On April 3, Scangos, who’s been chief executive officer at Vir since the start of 2017, will hand over the reins to Marianne De Backer, Ph.D. De Backer comes over from Bayer, where she currently heads up pharmaceutical strategy, business development and licensing. Alongside her CEO appointment, De Backer is set to join Vir’s board of directors, the company said Wednesday.

How can we help you?

We're easy to reach