Explore recent issues of Contract Pharma covering key industry trends.
Read the full digital version of our magazine online.
Behind every facility expansion, technology investment, and quality milestone in the CDMO sector is a leadership team making deliberate choices about where to focus, how to grow, and when to take calculated risks.
Stay informed! Subscribe to Contract Pharma for industry news and analysis.
Get the latest updates and breaking news from the pharmaceutical and biopharmaceutical industry.
Discover the newest partnerships and collaborations within the pharma sector.
Keep track of key executive moves and promotions in the pharma and biopharma industry.
Updates on the latest clinical trials and regulatory filings.
Stay informed with the latest financial reports and updates in the pharma industry.
A video roundup of the week’s top industry news stories.
Expert Q&A sessions addressing crucial topics in the pharmaceutical and biopharmaceutical world.
In-depth articles and features covering critical industry developments.
Access exclusive industry insights, interviews, and in-depth analysis.
Insights and analysis from industry experts on current pharma issues.
A one-on-one video interview between our editorial teams and industry leaders.
Listen to expert discussions and interviews in pharma and biopharma.
Contract Pharma Stream offers a centralized destination where users can watch expert-led sessions anytime, anywhere
A detailed look at the leading US players in the global pharmaceutical and BioPharmaceutical industry.
Browse companies involved in pharmaceutical manufacturing and services.
Comprehensive company profiles featuring overviews, key statistics, services, and contact details.
A comprehensive glossary of terms used in the pharmaceutical and biopharmaceutical industry.
Watch in-depth videos featuring industry insights and developments.
Download in-depth eBooks covering various aspects of the pharma industry.
Access detailed whitepapers offering analysis on industry topics.
View and download brochures from companies in the pharmaceutical sector.
Explore content sponsored by industry leaders, providing valuable insights.
Stay updated with the latest press releases from pharma and biopharma companies.
Explore top companies showcasing innovative pharma solutions.
Meet the leaders driving innovation and collaboration.
Engage with sessions and panels on pharma’s key trends.
Hear from experts shaping the pharmaceutical industry.
Join online webinars discussing critical industry topics and trends.
A comprehensive calendar of key industry events around the globe.
Live coverage and updates from major pharma and biopharma shows.
Find advertising opportunities to reach your target audience with Contract Pharma.
Review the editorial standards and guidelines for content published on our site.
Understand how Contract Pharma handles your personal data.
View the terms and conditions for using the Contract Pharma website.
What are you searching for?
Genentech will have license exclusivity, while DualityBio will lead discovery and early clinical development.
August 28, 2026
By: Patrick Lavery
Editor’s Take: As certain ADCs move into earlier lines of therapy across major solid tumor indications, an unmet need remains.
DualityBio will partner with Genentech to use the proprietary DualityBio Unique Payload Antibody Conjugate (DUPAC), developing next-generation antibody-drug conjugates (ADCs).
The collaboration and license agreement gives Genentech, a member of the Roche Group, exclusivity to ADCs produced from the partnership. DualityBio will generate and develop the ADCs against oncology targets Genentech defines, using payloads from the DUPAC platform.
DUPAC is dedicated to payloads with novel mechanisms of action, comprising multiple distinct payloads each built on unique antitumor mechanisms. These are then paired with optimized, compatible linker technologies that are designed for systemic stability and tumor-specific release.
DualityBio uses a common set of criteria to engineer DUPAC payloads. Among these: high potency, broad-spectrum activity across tumor types, short systemic half-life, and a bystander effect suited to heterogeneous tumors.
Topoisomerase inhibitor-based ADCs are moving into earlier lines of therapy across major solid tumor indications. This means that patients who progress on this payload class are indicative of a large, growing area of unmet need.
Highlighting this issue, John Zhu, PhD, DualityBio Founder and CEO.
“We built DUPAC to help address this challenge with a family of next-generation payloads designed to overcome resistance,” Zhu said. “We can advance these programs with greater speed and scale and bring differentiated medicines to more patients around the world.”
Boris L. Zaïtra, head of Roche Corporate Business Development, agreed.
“By further enhancing targeted medicines like ADCs, we focus our innovation where the need is highest,” Zaïtra said. “Collaborating with partners such as DualityBio enables us to identify novel treatment options, so we can tackle patients’ unmet needs.”
Financially, DualityBio receives a $45 million upfront payment. The company is then eligible to get more than $1 billion additionally through milestone payments across all programs.
Enter your account email.
A verification code was sent to your email, Enter the 6-digit code sent to your mail.
Didn't get the code? Check your spam folder or resend code
Set a new password for signing in and accessing your data.
Your Password has been Updated !