Stock Markets July 6, 2026 05:24 AM

Novartis to Buy Myricx Bio for $1.1 Billion to Add Novel ADC Payload Platform

Deal brings N-myristoyltransferase inhibitor payloads and two lead ADC candidates targeting B7-H3 and HER2 to Novartis' oncology pipeline

By Ajmal Hussain
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Novartis has agreed to acquire UK-based Myricx Bio for $1.1 billion upfront plus up to $400 million in contingent milestones. The acquisition brings a potential first-in-class N-myristoyltransferase inhibitor (NMTi) antibody-drug conjugate (ADC) payload platform — intended to address resistance to existing ADC payloads — and two lead ADC assets aimed at B7-H3 and HER2 into Novartis' oncology portfolio. The transaction is expected to close in the second half of 2026, subject to customary conditions and regulatory approvals.

Novartis to Buy Myricx Bio for $1.1 Billion to Add Novel ADC Payload Platform
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Key Points

  • Novartis will acquire Myricx Bio for $1.1 billion upfront plus up to $400 million in milestone payments.
  • The acquisition adds a potential first-in-class NMTi ADC payload platform aimed at overcoming resistance to current ADC payloads.
  • Two lead ADC candidates targeting B7-H3 and HER2 join Novartis' oncology pipeline, with potential application across multiple solid tumor types.

Novartis has entered into a definitive agreement to acquire Myricx Bio, a privately held biotechnology firm based in the United Kingdom, for $1.1 billion in upfront consideration and up to $400 million in additional milestone payments.

The deal will add a novel ADC payload platform that uses N-myristoyltransferase inhibitors (NMTi) to Novartis' suite of oncology assets. The platform is described as potentially first-in-class and was developed with the stated aim of tackling resistance mechanisms that limit the effectiveness of existing ADC payload classes.

Myricx Bio's approach deploys NMTi payloads within antibody-drug conjugates to deliver a cytotoxic agent directly to tumor cells. The company positions this mechanism as a response to constraints associated with commonly used ADC payload families, including TOPO-1 inhibitors, by offering an alternative intracellular target.

The acquisition brings two lead ADC candidates into Novartis' clinical development pipeline. Both assets are directed against established oncology targets - B7-H3 and HER2 - and are positioned for potential use across multiple solid tumor indications.

"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.

At a mechanistic level, N-myristoyltransferase is an enzyme that enables key proteins to function inside cells, a process that supports cancer cell growth and survival. Myricx's NMTi payload is intended to inhibit that enzyme and thereby disrupt cellular processes cancer cells depend on.

According to preclinical data provided with the announcement, the NMTi payload has shown activity in models of solid tumors, including models that are resistant to TOPO-1 inhibitors. Those preclinical findings form part of the rationale Novartis cited for the acquisition.

The transaction is expected to complete in the second half of 2026, contingent on customary closing conditions and receipt of required regulatory approvals.


Context and implications

The deal expands Novartis' ADC capabilities by adding a distinct payload strategy and two disease-targeted assets, reinforcing its portfolio in solid tumor oncology development.

Risks

  • Completion of the transaction depends on customary closing conditions and regulatory approvals - any delay or failure in approvals could affect the timing or completion of the acquisition (impacts healthcare and corporate M&A activity).
  • Preclinical activity does not guarantee clinical efficacy - the NMTi payload's activity in preclinical models, including TOPO-1 resistant models, may not translate to successful human clinical outcomes (impacts biotech and pharmaceutical R&D risk).

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