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Roche announces global collaboration with Nurix Therapeutics to co-develop and co-commercialise potential best-in-class BTK degrader bexobrutideg across malignant haematology, immunology and neurology

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Roche (OTCQX:RHHBY) entered an exclusive global licensing and collaboration agreement with Nurix Therapeutics to co-develop and co-commercialise bexobrutideg (NX-5948), an oral BTK degrader for B-cell malignancies, immunology and neurology.

Bexobrutideg is planned to enter Phase 3 CLL trials in summer 2026. Nurix receives $700 million upfront and may earn up to $2.3 billion in total deal value, including milestones. Development costs are shared 60% Roche / 40% Nurix, with 50/50 U.S. profit and loss sharing and ex-U.S. royalties for Nurix in the low- to high-teens.

The transaction is subject to customary conditions, including Hart-Scott-Rodino clearance, and is expected to close in the third quarter of 2026.

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Positive

  • Upfront payment of $700 million secures global rights to bexobrutideg
  • Potential total deal value up to $2.3 billion aligns incentives with Nurix
  • Roche funds 60% of development while gaining 50% of U.S. profits
  • Co-commercialisation in the U.S. with profit/loss split diversifies revenue exposure
  • Exclusive ex-U.S. commercial rights with tiered royalties to Nurix
  • Planned Phase 3 CLL start in summer 2026 advances malignant haematology pipeline

Negative

  • Roche commits to $700 million upfront plus up to $2.3 billion in milestones
  • Roche bears 60% of global development costs for bexobrutideg
  • Bexobrutideg remains investigational with Phase 3 trials yet to commence
  • Transaction closing is contingent on Hart-Scott-Rodino waiting period expiration or termination

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  • Agreement offers potential best-in-class targeted protein degrader therapy option for people living with B-cell malignancies
  • Collaboration adds to Roche’s oncology pipeline and offers potential indications in immunology (chronic spontaneous urticaria) and neurology (multiple sclerosis)
  • Bexobrutideg utilises a novel approach to eliminate the Bruton’s Tyrosine Kinase (BTK) protein, potentially overcoming existing resistance mechanisms found with current standard-of-care BTK inhibitors

Basel, 08 June 2026 - Roche (SIX: RO, ROP; OTCQX: RHHBY) announced today that it has entered into an exclusive licensing and collaboration agreement with Nurix Therapeutics, Inc. (Nasdaq: NRIX). Under the terms of this agreement, the two companies will collaborate to co-develop and co-commercialise bexobrutideg (NX-5948), Nurix’s investigational Bruton’s Tyrosine Kinase (BTK) degrader. The collaboration encompasses a clinical development plan spanning B-cell malignancies, immunology and neurology. The addition of bexobrutideg complements Roche’s existing strengths in haematology and provides a cross-therapeutic opportunity to extend the pipeline's reach in immunology and neurology.

Patients with B-cell–driven malignancies continue to face significant unmet need despite advances with BTK inhibitors and other therapies. In haematology, many patients with CLL ultimately experience disease progression due to acquired resistance mutations, incomplete pathway suppression, or intolerance that limits long-term use, and treatment options remain limited once patients relapse.

BTK-targeting assets represent a leading class within the expanding non-Hodgkin lymphoma (NHL) and CLL markets. The combined market is projected to reach $41 billion by 2031, with BTK inhibitors (BTKi) expected to remain the sales-leading class at approximately $19 billion.¹ This growth is particularly evident in the CLL sector, which is forecast to increase from $12 billion in 2024 to $16 billion by 2035.²

Bexobrutideg, an oral targeted BTK degrader, is planned for Phase 3 clinical trial initiation in summer 2026 for the second-line treatment of CLL. Available clinical data suggests it has the potential to become a best-in-class treatment option with higher efficacy and more favorable tolerability than established therapies. In addition, it offers the potential to overcome resistance mechanisms found in current standard-of-care BTK inhibitors. This collaboration creates a unique opportunity to leverage Roche’s industry-leading malignant haematology portfolio.

Levi Garraway, Roche Chief Medical Officer and Head of Global Product Development: “At Roche, our goal is to create new possibilities for patients with challenging diseases. We believe bexobrutideg could represent a major leap forward in the fight against complex blood cancers and other diseases. We are proud to join forces with Nurix to accelerate these potential breakthroughs.”

Arthur T. Sands, M.D., Ph.D., president and chief executive officer of Nurix Therapeutics: “We believe Roche is the ideal partner to help translate the promise of targeted protein degradation into meaningful impact for patients worldwide. As a single agent, bexobrutideg has shown highly promising results in B cell malignancy clinical trials to date and we can now rapidly expand our Phase 3 program enhanced by Roche’s global reach. We are also excited to explore combination regimens utilising selected agents from Roche’s portfolio of successful B-cell malignancy drugs. In addition, collaborating with Roche uniquely enables our ability to extend the cross-therapeutic opportunity of bexobrutideg in immunology and neurology.”

While BTK is a proven target in B-cell malignancies, it is also a critical signaling node driving various conditions in immunology and neurology. Because of bexobrutideg's ability to eliminate both the kinase and scaffolding functions of BTK across immune cell types it has the potential for improved efficacy and durability in these diseases.

Terms of the agreement
Under the terms of the agreement, Nurix will receive an upfront cash payment of USD 700 million and is eligible to receive development, regulatory and sales milestones for a potential total deal value of up to USD 2.3 billion. Development costs will be shared 40% by Nurix and 60% by Roche. The parties will equally split the profits and losses from U.S. commercialisation. Nurix and Roche will co-commercialise bexobrutideg in the United States across all indications. Outside of the United States, Roche will be responsible for commercialisation, with Nurix receiving royalties ranging from the low- to high-teens.

The transaction is subject to customary closing conditions, including the expiration or termination of the waiting period under the Hart-Scott-Rodino Antitrust Improvements Act of 1976. The parties currently expect the transaction to close in the third quarter of 2026.

About bexobrutideg
Bexobrutideg (NX-5948) is an investigational, orally bioavailable, brain-penetrant BTK degrader for the treatment of relapsed or refractory B-cell malignancies and potentially diseases in immunology and neurology. BTK is a central signaling node controlling B cell growth, development and immunologic activity. Unlike conventional BTK inhibitors, which block BTK kinase activity, bexobrutideg harnesses the body's natural protein disposal system. Bexobrutideg selectively eliminates BTK protein from cells, removing both its kinase activity and scaffolding function, potentially overcoming existing treatment-emergent resistance mutations and unlocking new therapeutic potential of targeting BTK.

About malignant haematology
B-cell malignancies, including chronic lymphocytic leukaemia (CLL), represent a significant health challenge where recent scientific advances can help meet high unmet medical needs. CLL is a slow-growing cancer in the blood and bone marrow and is one of the most common forms of leukemia in adults. While outcomes have improved in recent years, patients often face long treatment durations and ongoing disease management challenges. Although signs of CLL may disappear for a while after initial treatment, many people require additional treatment due to the return of cancerous cells.

About CSU and MS
CSU is a debilitating, long-term, immune mediated skin condition characterized by recurring, itchy hives. MS is a chronic disease affecting nearly 3 million people worldwide. It occurs when the immune system attacks the protective covering of nerves in the brain and spinal cord, disrupting signals throughout the body and causing movement and neurological challenges.

About Roche
Roche (SIX: RO, ROP; OTCQX: RHHBY) is a healthcare company uniquely placed to prevent, stop and cure diseases by uniting leading science and technology across diagnostics, medicines and digital solutions.

Roche was founded in Basel, Switzerland in 1896 and today is a leading provider of transformative medicines and diagnostics for millions of people in over 150 countries around the world. It is dedicated to tackling healthcare challenges that place the greatest strain on patients, families, communities and healthcare systems. Across its Diagnostics and Pharmaceutical divisions, Roche focuses on areas including oncology, neurology, cardiovascular and metabolic diseases, ophthalmology, infectious diseases and immunology with the aim of providing real and positive change for patients, the people they love and the professionals who care for them.

Genentech in the United States is a fully owned subsidiary in the Roche Group. Roche is the majority shareholder in Chugai Pharmaceutical, a major innovator in the Japanese therapeutic antibody market.

For more information, please visit www.roche.com.

All trademarks used or mentioned in this release are protected by law.

References
[1] Clarivate, NHL/CLL Disease Landscape and Forecast, 2024.
[2] DRG (Decision Resources Group) & Datamonitor Healthcare, CLL Market Analysis, 2025.

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FAQ

What did Roche (RHHBY) announce about its collaboration with Nurix on bexobrutideg?

Roche announced an exclusive global licensing and collaboration deal with Nurix to co-develop and co-commercialise bexobrutideg across oncology, immunology and neurology. According to Roche, the agreement focuses on B-cell malignancies and expands potential indications into chronic spontaneous urticaria and multiple sclerosis.

How much is Roche paying Nurix in the June 2026 bexobrutideg (RHHBY) deal?

Roche will pay Nurix a $700 million upfront cash payment and up to $2.3 billion in total deal value. According to Roche, the additional amount includes development, regulatory and sales milestones tied to bexobrutideg’s progress and commercial performance.

How are development costs and U.S. profits shared in the Roche–Nurix bexobrutideg collaboration (RHHBY)?

Development costs for bexobrutideg will be split 60% by Roche and 40% by Nurix, with equal U.S. profit and loss sharing. According to Roche, both companies will co-commercialise in the United States across all indications.

When will Phase 3 trials of bexobrutideg for CLL start under Roche (RHHBY) and Nurix?

Phase 3 clinical trial initiation of oral BTK degrader bexobrutideg for second-line CLL is planned for summer 2026. According to Roche, existing clinical data suggest potential best-in-class efficacy and tolerability compared with established Bruton’s Tyrosine Kinase therapies.

What therapeutic areas will Roche and Nurix target with bexobrutideg in the RHHBY agreement?

Roche and Nurix will target malignant haematology, immunology and neurology indications with bexobrutideg, including CLL, chronic spontaneous urticaria and multiple sclerosis. According to Roche, BTK’s role across immune cell types supports cross-therapeutic development opportunities.

How will ex-U.S. commercialisation of bexobrutideg work in the Roche–Nurix (RHHBY) deal?

Outside the United States, Roche will lead commercialisation of bexobrutideg and pay Nurix tiered royalties from the low- to high-teens. According to Roche, this structure grants Roche global reach while providing Nurix with ongoing ex-U.S. revenue participation.

When is the Roche and Nurix bexobrutideg (RHHBY) transaction expected to close?

The transaction is expected to close in the third quarter of 2026, subject to customary conditions. According to Roche, closing depends on expiration or termination of the Hart-Scott-Rodino waiting period and other standard regulatory clearances.