Skip to content

Project

Intismeran autogene

Personalized mRNA cancer vaccine made from each patient's tumor mutations, developed by Moderna and Merck under the codes mRNA-4157/V940.

Known aliases

  • individualized neoantigen therapy
  • INT
  • intismeran
  • Moderna-Merck personalized cancer vaccine
  • mRNA-4157
  • mRNA-4157/V940
  • V940

Current stories

scienceOne report1 publisher

Merck and Moderna weigh which tumors to test next for their melanoma vaccine

Merck and Moderna are preparing to file their personalized mRNA melanoma vaccine after a Phase 3 trial showed it delayed recurrence. At the STAT Summit, executives said the next task is showing it works in other tumors, and that they must pick where to look first.

Publishers:statnews.com

Reality

Evidence40
Adoption
Not scored
Hype gap+15
Incentives60
Confidence55
scienceOne report1 publisher

Merck and Moderna's melanoma result leaves the next target for mRNA cancer vaccines unsettled

Merck and Moderna's mRNA vaccine intismeran autogene slowed the return and spread of melanoma when added to an existing treatment in a late-stage trial. One trial cannot say which other cancers the same approach can treat.

Publishers:statnews.com

Reality

Evidence35
Adoption
Not scored
Hype gap+10
Incentives40
Confidence40
investConfirmed6 publishers

Moderna doubles on a Phase 3 win whose effect size has not been published yet

Intismeran autogene plus Keytruda beat Keytruda alone in resected melanoma. The market added roughly $35bn to Moderna on a result the companies described only in adjectives.

Perspective Coverage

6 publishers
Builder
Builder 29%
Operator
Operator 25%
Investor
Investor 46%

Reality

Evidence45
Adoption5
Hype gap+55
Incentives70
Confidence60
productConfirmed3 publishers

Moderna's per-patient cancer vaccine cleared Phase 3. Now it is a manufacturing problem.

Intismeran autogene met both primary endpoints in a 1,137-patient melanoma trial. Every dose is built from one tumour's sequence, which turns approval into a question about process, not product.

Perspective Coverage

3 publishers
Builder
Builder 38%
Operator
Operator 42%
Investor
Investor 20%

Reality

Evidence40
Adoption5
Hype gap+40
Incentives75
Confidence55
scienceConfirmed4 publishers

Merck and Moderna clear the Phase 3 bar on a personalized cancer vaccine, minus the numbers

The companies say intismeran plus Keytruda slowed melanoma's return after surgery in the first randomized Phase 3 test of neoantigen vaccines. No detailed data has been released.

Perspective Coverage

4 publishers
Builder
Builder 39%
Operator
Operator 36%
Investor
Investor 25%

Reality

Evidence40
Adoption3
Hype gap+40
Incentives70
Confidence55
scienceConfirmed3 publishers

Phase III for a bespoke mRNA cancer therapy repriced the sequencing vendors, not just Moderna

Merck and Moderna put out no efficacy figures. Illumina still rose 16% and PacBio 18%, because an approved per-patient therapy implies a sequencing run per patient.

Perspective Coverage

3 publishers
Builder
Builder 27%
Operator
Operator 32%
Investor
Investor 41%

Reality

Evidence45
Adoption
Not scored
Hype gap+40
Incentives55
Confidence55
investOne report1 publisher

Tempus AI's 31.91% week supplied nine points of a Korean ETF's 19.56% return

Hana Asset Management's medical AI fund led every ETF listed in South Korea last week, helped by a Morgan Stanley estimate that Medicare coverage could add $330m to $400m of annual revenue at its largest holding.

Publishers:en.sedaily.com

Reality

Evidence45
Adoption
Not scored
Hype gap+40
Incentives75
Confidence45
scienceOne report1 publisher

Software picks the 34 neoantigens in Moderna and Merck's cancer vaccine

Intismeran autogene would arrive with a selection procedure where other drugs have a fixed molecule, and the outside expert STAT asked could not say what the software weighs. That makes the ranking code the hard part of any review.

Publishers:statnews.com

Reality

Evidence34
Adoption21
Hype gap+32
Incentives66
Confidence41
investOne report1 publisher

An mRNA vaccine cleared Phase 3 on Keytruda, and the read-through lands on Alteogen

Moderna and MSD's V940 hit both endpoints in adjuvant melanoma. The commercial consequence sits with Keytruda SC, whose conversion rate reached 10.6% in July.

Publishers:en.sedaily.com

Reality

Evidence52
Adoption44
Hype gap+24
Incentives72
Confidence45