US-based biopharmaceutical company Epizyme has entered into a collaboration agreement with Genentech, a member of the Roche Group, to carry out a clinical trial to evaluate the anti-cancer effects of tazemetostat in combination with Tecentriq (atezolizumab) to treat non-hodgkin lymphoma (NHL).

Tazemetostat is Epizyme’s clinical-stage EZH2 inhibitor, while Tecentriq is Genentech’s recently approved anti-PD-L1 cancer immunotherapy.

Discover B2B Marketing That Performs

Combine business intelligence and editorial excellence to reach engaged professionals across 36 leading media platforms.

Find out more

Patients afflicted with relapsed or refractory diffuse large B-cell lymphoma (DLBCL) will be administered with a combination regimen of the two medical products.

Epizyme president and CEO Robert Bazemore said: "A key part of Epizyme’s long-term vision is expanding the benefit that tazemetostat can bring to patients, and includes combining tazemetostat with checkpoint inhibitors.

"This collaboration aligns us with a global leader in oncology and hematology, and advances Epizyme’s leadership position in the development of epigenetic therapeutics."

"We believe this study will be enhanced by our partner’s deep expertise in the field of immuno-oncology.

"This collaboration aligns us with a global leader in oncology and hematology, and advances Epizyme’s leadership position in the development of epigenetic therapeutics."

GlobalData Strategic Intelligence

US Tariffs are shifting - will you react or anticipate?

Don’t let policy changes catch you off guard. Stay proactive with real-time data and expert analysis.

By GlobalData

As part of the deal, Genentech will be responsible for managing the planned clinical trial.

The planned Phase Ib clinical trial will start enrolling patients in the second half of this year.

Tazemetostat is a first-in-class small molecule created by Epizyme based on its patented product platform, and is indicated to treat NHL and certain genetically defined solid tumours

It inhibits EZH2, which is responsible in triggering dysregulation of genes that control cell proliferation, leading to a rapid and unconstrained growth of tumour cells.

Tecentriq recently received accelerated approval from the US Food and Drug Administration (FDA) for people with a specific type of advanced bladder cancer.

Clinical Trials Arena Excellence Awards - Nominations Closed

Nominations are now closed for the Clinical Trials Arena Excellence Awards. A big thanks to all the organisations that entered – your response has been outstanding, showcasing exceptional innovation, leadership, and impact

Excellence in Action
Science 37 has won the Research and Development Award in the Site Innovation category for its FDA inspected Direct-to-Patient Site model, delivering nationwide access, faster enrollment and higher retention. Explore how its virtual-first, in home approach is reshaping trial operations and accelerating time to data-driven decisions..

Discover the Impact