INSIGHTS

Lipid Cuts, Big Deals, and a New CRISPR Era

CRISPR Therapeutics’ early data, major deals, and new diagnostics fuel rapid momentum in gene editing

24 Nov 2025

Eli Lilly corporate building with prominent red Lilly logo on modern glass façade.

The gene editing field is moving with fresh urgency. CRISPR Therapeutics has released early trial results for its one time therapy, CTX310, showing sharp reductions in blood fats tied to heart disease and stirring broad excitement across biotech.

The treatment cut ANGPTL3 by 73% while trimming triglycerides and LDL cholesterol by about one half. Although the data are early, the consistency of these shifts has energized scientists who have long waited for clear signs that gene edits can deliver reliable clinical effects. One senior researcher at the company called the findings a turning point and said the edits are behaving in a stable and predictable way.

Momentum is also rising through high profile deals. Verve Therapeutics, a leading name in cardiovascular gene editing, is set to join Eli Lilly’s growing heart disease portfolio in a transaction valued at up to US$1.3 billion and projected to close in the third quarter of 2025. Analysts view the move as evidence that major drugmakers now see genetic medicines as anchors for future treatment strategies.

Diagnostics are gaining speed as well. Mammoth Biosciences is expanding its CRISPR based testing platform through new partnerships, including a licensing agreement with VedaBio that aims to deliver faster and more precise diagnostic tools. The effort broadens access to gene editing technologies and strengthens the surrounding ecosystem.

Challenges remain on the road to everyday use. Permanent DNA edits demand rigorous regulatory scrutiny, long term safety data, and clear evidence for insurers evaluating coverage of high cost therapies. Production at scale continues to pose technical hurdles.

Even so, confidence is building. Each advance, from clinical data to corporate moves, fuels expectations that CRISPR may soon reshape treatment for widespread diseases. The next wave of results could push the field even closer to that reality.

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