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Myricx Bio to be Acquired by Novartis to Advance Next-Generation ADC Payloads for Oncology with Novel NMTi Platform

Key Takeaway: Myricx Bio has announced its acquisition by Novartis for up to $1.5 billion, including $1.1 billion in cash upfront. This acquisition aims to leverage Novartis's oncology expertise and Myricx's innovative N-myristoyltransferase inhibitor (NMTi) payload platform, which has potential applications across various solid tumors. The deal is expected to close in the second half of 2026, pending regulatory approvals.
Price reaction · baseline $159.9 (2026-07-02 close) · hit pre-market · 1 other NVS headline(s) in the window, move may be shared
day 0 close · peak
-2.8%

Market Sentiment Analysis

POSITIVE FACTORS

  • Novartis acquires Myricx Bio to enhance ADC innovation.
  • The NMTi platform offers a differentiated mechanism of action.
  • Transaction valued at up to $1.5 billion indicates strong market confidence.
  • Potential to address significant unmet needs in oncology.

BiopharmaWatch Analysis

From our catalyst data and publicly available data · not financial advice
Best trade, last catalyst
+25%
120-day peak, hindsight
Typical move
1.9%
average across 15 past catalysts
Lead asset
Vildagliptin
Phase 1 · Healthy

Full Press Release Details

• Potential first-in-class N-myristoyltransferase inhibitor (NMTi) ADC payload with a differentiated mechanism of action
• Combines oncology expertise of Novartis with Myricx Bio’s novel ADC assets and platform having broad potential across multiple solid tumour types
• Transaction valued at up to $1.5 billion including $1.1 billion cash upfront
LONDON, July 06, 2026 (GLOBE NEWSWIRE) -- Myricx Bio, a UK-headquartered biotech company focusing on the discovery and development of a novel class of payloads for antibody-drug conjugates (ADCs), today announced that it has reached agreement to be acquired by Novartis for up to $1.5 billion including $1.1 billion cash upfront plus potential milestone payments.
The acquisition advances ADC innovation by bringing together the strengths of Novartis in oncology with Myricx Bio’s two lead ADC assets and next-generation first-in-class N-myristoyltransferase inhibitor (NMTi) payload platform, having potential impact across multiple solid tumour settings.
Since its founding in 2019, Myricx Bio has translated its founders’ extensive research and world leading insights in NMT biology and chemistry into ADC payloads with a novel, orthogonal and differentiated mode of action to address limitations of commonly used ADC payload classes such as TOPO-1 and tubulin inhibitors. Myricx Bio has advanced a pre-clinical pipeline of proprietary NMTi-ADCs with lead assets directed towards established targets B7-H3 and HER2.
“There is a widely recognised and critical unmet need for new ADC payloads that can improve the standard of care over current payloads, overcome payload resistance, improve tolerability and offer a wider therapeutic index. We are delighted that Novartis recognises the transformative promise of our NMTi-ADC platform to deliver this next-generation of potential first-in-class, highly differentiated ADC therapeutics,”said Mohit Rawat, CEO of Myricx Bio. “This acquisition is a tremendous endorsement of the leadership of our NMTi-ADC platform, and the insights, innovation and achievements of our founders and team towards our mission of providing more effective and better tolerated therapeutic options for cancer patients. Together with Novartis, we look forward to building upon our work to transform the landscape of cancer treatment.”
“ADCs have become an important part of cancer treatment, but there remains a clear need for new payload mechanisms to overcome resistance and expand their impact for patients,”said Fiona Marshall, President of Biomedical Research at Novartis. “Myricx Bio has developed a promising NMTi payload platform with a differentiated mechanism that could broaden the use of ADCs across multiple tumour settings. This proposed acquisition reflects our strategy to scale innovative platforms, as we have with radioligand therapies, to deliver more durable, transformative treatments for patients.”
Myricx Bio was spun out from Imperial College London and the Francis Crick Institute, by Professor Ed Tate Ph.D., Roberto Solari Ph.D. and Andrew Bell Ph.D., supported by Cancer Research UK, and backed by seed investment from Brandon Capital and Sofinnova Partners. Under the leadership of current Myricx Bio CTO, Robin Carr Ph.D., the company raised £90m ($114m) in a Series A in mid-2024 led by Novo Holdings and Abingworth who were joined by British Business Bank, Cancer Research Horizons and Eli Lilly, and existing investors. This enabled the company to scale its operations and expand the team to rapidly advance its pipeline. Mohit Rawat joined as CEO in 2025 to steer the company through pre-clinical development and its next stage of growth, leading to this groundbreaking deal.
The transaction is expected to close in H2 2026, subject to the satisfaction or waiver of customary closing conditions, including regulatory approvals.
Goodwin was legal advisor to Myricx Bio through the transaction.

Caption:Mohit Rawat, Myricx Bio CEO

Copyright:Myricx Bio

Access to a media library of high-resolution photographs atMyricx Bio Media Kit

At the CompanyMohit Rawat, CEO, Myricx Bio,info@myricxbio.com

Media EnquiriesCharles ConsultantsSue Charles -Sue@charles-consultants.com+44 (0)7968 726585Chris Gardner -Chris@CGComms.onmicrosoft.com+44 (0)7956 031077

Notes to Editors:

About N-myristoyltransferase inhibition and ADCs

N-myristoyltransferase (NMT) is an enzyme responsible for the addition of a specific lipid to multiple proteins that are crucial for cancer cell survival. Myricx Bio has developed a pipeline of antibody-drug conjugates (ADCs) to address significant unmet needs in oncology, leveraging its NMT inhibitor (NMTi) payload chemistry platform. These ADCs have demonstrated exceptional preclinical efficacy and tolerability across multiple solid tumour-associated antigens and cancer cell types.
Retreatment with ADCs with the same payload class leads to poor outcomes with a >50% reduction in the objective response rate (ORR). Toxicity is currently a major challenge for ADCs often limiting tolerable ADC doses to levels below those required for substantial anti-cancer efficacy. Many of the leading ADCs have >50% treatment interruptions or dose reductions due to adverse effects. There is thus an urgent need for novel and differentiated ADC payloads.
NMT is critical to maintaining multiple pathways required for cancer cell survival. Pre-clinical observations suggest inhibition of this enzyme drives complete tumour regression, including in challenging tumour types. In addition, due to the completely novel MOA, NMTi-ADCs have a differentiated toxicity profile and the potential to treat cancers that have become resistant to or are unresponsive to current ADCs.

About Myricx Bio -www.myricxbio.com

Myricx Bio (“Myricx Bio”) is a private biotechnology company focused on the discovery and development of therapeutics for the treatment of patients with cancer. It has pioneered the development of a completely novel class of payloads for antibody-drug conjugates (ADCs), based on inhibition of N-myristoyltransferase (NMT).
A spin out from Imperial College London and the Francis Crick Institute, Myricx Bio is headquartered in London with teams based in the UK and USA. Investors include Abingworth, Brandon Capital Partners, British Business Bank, Cancer Research Horizons, Eli Lilly, Novo Holdings and Sofinnova Partners.
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Frequently Asked Questions

What is the value of the acquisition deal?

The acquisition deal is valued at up to $1.5 billion, including $1.1 billion cash upfront.

What is the NMTi platform developed by Myricx Bio?

The NMTi platform is a novel payload mechanism for antibody-drug conjugates aimed at improving cancer treatment.

When is the acquisition expected to close?

The transaction is expected to close in the second half of 2026, pending regulatory approvals.

What are the potential benefits of the NMTi payload?

The NMTi payload has the potential to overcome resistance and improve tolerability in cancer therapies.

Last updated: Jul 6, 2026