Jason Mast
Editor
Joan Butterton
Joan Butterton was sitting 30,000 feet above the Atlantic, flying to a conference in Europe, when the Merck scientist seated next to her started gushing about the HIV molecule the big pharma had just licensed from a small Japanese company. It was so potent in monkeys, the scientist said, that they couldn’t figure out what the lowest effective dose was and it stayed in the animals for an incredibly long time, far longer than the approved drugs HIV patients took daily.
Nine years and a few clinical trials later, Merck has shown that the drug, islatravir, can keep patients’ viruses suppressed with just one pill. Now Butterton, who now runs Merck’s late-stage infectious disease trials, will try to chart a blockbuster future for the drug, as the NJ pharma teams with a longtime rival to make it the base of a franchise that remakes HIV treatment.
In a rare collaboration between two of the biggest HIV drug developers, Merck and Gilead announced Monday that they will collaborate to turn one of the most promising molecules from each of their pipelines into a two-drug combo that can provide patients options outside of the daily pills that have dominated the field for years.
“Really, we’re seeing this drug as something that is foundational,” Butterton told Endpoints News.
With the deal, Merck and Gilead will combine two molecules with different mechanisms that have already shown efficacy in the clinic. Merck’s islatravir is a new kind of reverse transcriptase inhibitor, singlehandedly mucking up two different processes the virus relies on to replicate. Gilead’s lenacapavir, which they recently showed could effectively reduce viral levels in patients with drug-resistant HIV, inhibits the HIV’s shell, commonly called its capsid.
The idea is that the combo could become a potent once-a-week pill and, in another formulation, an injectable that patients can take as infrequently as once every six months. Either of those accomplishments would instantly make the drug a leading contender in one of the competitive fields in HIV: the hunt for a long-acting drug.
It’s an important branch of medicine, potentially helping patients who struggle with or face stigma taking a daily pill. And it’s currently led by GlaxoSmithKline’s spinout ViiV, which won approval this year for a first-of-its-kind once-a-month shot for HIV patients.
Merck and Gilead are already gaming out the potential for a blockbuster laying out terms for how profit sharing will change if annual sales exceed $2 billion or $3.5 billion, depending on whether it’s the oral or injectable form.
Diana Brainard
In an interview, Gilead HIV chief Diana Brainard called the collaboration “historic,” touting the potential for the cocktail to give new options for patients with HIV.
“They’re both highly potent,” Brainard said of the two molecules. “The more potent the drug is, the lower the dose is and when you’re looking at long-acting, that’s important because you have to give a whole weeks of a dose, or whole three months worse of a dose in one oral pill or one injection.”
Analysts praised the deal for both teams. Piper Sandler’s Tyler Van Buren said it was a “direct acknowledgment” from Gilead that after years of a one-sided race between the two drugmakers, Merck finally has a molecule that can compete. Jefferies’ Michael Yee said it was an “incremental positive” for Gilead that would allow them to take a larger share of the market in the long term.
The two companies will now combine the new drugs in multiple trials, testing both pills and injectable forms. The first study will test an oral combo and begin in the second half of this year. Because Gilead and Merck have yet to devise a formula that combines the molecules into a single pill, the first volunteers will simply take one of each.
The companies also have work to do on creating a single injectable formulation, Brainard said, a complicated task that could determine how long the shot will last. They hope to have one formulation complete next year.
Gilead and Merck will split costs 60/40. They will share profits 50/50 unless sales exceed $2 billion per year for the oral formula or $3.5 billion for the injectable formula. At that point, Gilead would begin taking 65% of sales. Both companies have another type of molecule, an integrase inhibitor, in trials. In the deal, Merck gave Gilead an option to license their integrase inhibitor and vice versa.
The long-acting treatment program represents just one of several applications each developer has for their molecules, alongside use in drug-resistant patients and as pre-exposure prophylaxis to prevent infection. Merck thinks an implant of islatravir alone could protect patients from an HIV for a year — an application that’s still in early development but which would provide the closest thing the field has to a vaccine.
“At Merck, we are resolute in our commitment to advancing the care of people living with HIV as part of our mission to save and improve lives,” Merck CEO Ken Frazier said in a statement. “This collaboration with Gilead brings together two companies dedicated to the fight against HIV to develop potential new long-acting treatment options, and is an important step forward in our strategy to harness the full potential of islatravir for the treatment of HIV.”
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