Merck pays Moderna $250m for personalized cancer vaccine

The shot is designed to stop skin cancer from returning after surgery.

Pharma giant Merck has paid Moderna $250 million to co-develop and commercialize a promising personalized cancer vaccine based on its mRNA technology.

The background: In 2016, pharma giant Merck gave Moderna $200 million to research and develop personalized cancer vaccines based on mRNA. At the time, it was a big bet — mRNA technology had yet to be translated into any approved vaccine.

Part of the original agreement specified that if Moderna could complete proof-of-concept studies of mRNA-based personalized cancer vaccines in humans, Merck had the option to pay an undisclosed amount to co-develop and commercialize the shots with Moderna.

Since then, mRNA has proven itself with the development of COVID-19 vaccines, and many other vaccines are in development. And now, based on that success, they’re moving ahead with cancer vaccines, too.

Most vaccines are mass produced, but Moderna’s cancer vaccine is personalized for each patient.

What’s new? Merck is now exercising its option on mRNA-4157, a personalized cancer vaccine in a phase 2 clinical trial for skin cancer. It’s being studied in combination with Merck’s cancer treatment Keytruda, a humanized monoclonal antibody.

“This long-term collaboration combining Merck’s expertise in immuno-oncology with Moderna’s pioneering mRNA technology has yielded a novel tailored vaccine approach,” said Eliav Barr, head of global clinical development and CMO of Merck Research Laboratories. 

A personalized cancer vaccine: Moderna’s cancer vaccine works differently than most vaccines because it’s designed to treat an existing disease rather than prevent it entirely. It’s also personalized for each patient, while other shots are typically mass produced and distributed to the population.

To create each vaccine, Moderna takes a sample of a patient’s tumor. It then uses genetic sequencing technology to identify proteins in the tissue called “neoantigens.” These proteins are found only on the surface of cancer cells, and they are unique to each person’s tumor.

Moderna then uses its mRNA technology to create a vaccine that instructs cells to make up to 34 of the cancer’s specific neoantigens, which are shown off to immune cells as potential targets. The idea is that this will trigger an immune response against the neoantigens, helping the immune system identify and attack cancerous cells.

Given Merck’s new investment in the vaccine, it seems reasonable to expect positive trial results.

Looking ahead: For Moderna’s ongoing phase 2 trial of mRNA-4157, 157 patients with high-risk melanoma had their tumors removed via surgery. 

Some of the patients were then given nine doses of a personalized cancer vaccine and a dose of Keytruda every three weeks for approximately one year or until their melanoma came back. The rest were given just a dose of Keytruda every three weeks for one year.

The trial’s primary endpoint is recurrence-free survival, and given Merck’s new investment in the vaccine, it seems reasonable to expect positive results.

“With data expected this quarter on [personalized cancer vaccine], we continue to be excited about the future and the impact mRNA can have as a new treatment paradigm in the management of cancer,” said Moderna President Stephen Hoge.

We’d love to hear from you! If you have a comment about this article or if you have a tip for a future Freethink story, please email us at [email protected].

New brain cancer vaccine completes clinical trial
Northwest Biotherapeutics reports that its new brain cancer vaccine can extend glioblastoma patients’ lives by months or even years.
New chemo pump for brain tumors could avoid side effects
A fully implantable chemo pump could help extend the lives of people with deadly brain tumors while minimizing treatment side effects.
UK study suggests single dose of monkeypox vaccine is 78% effective
A new analysis by the UK Health Security Agency has determined that one shot of a monkeypox vaccine is 78% effective at preventing infection.
$3.5 million treatment for hemophilia wins FDA approval
The FDA has approved biotech company CSL Behring’s Hemgenix, a hemophilia B treatment that costs $3.5 million per dose.
New CRISPR cancer treatment tested in humans for first time
A new personalized CRISPR cancer treatment modifies the immune system’s T cells to help them recognize a specific patient’s tumor cells.
Up Next
Subscribe to Freethink for more great stories