CytomX Therapeutics Announces 2026 Business Update and Milestones
Source: GlobeNewsWire
CytomX Therapeutics (CTMX) Provides Key Updates on Clinical Trials
SOUTH SAN FRANCISCO, Calif. - CytomX Therapeutics, Inc. (Nasdaq: CTMX), a leader in conditionally activated biologics, announced significant business updates and anticipated milestones for 2026 on January 8. Key developments include progress on the CX-2051 (varsetatug masetecan) for colorectal cancer and ongoing studies for the CX-801 (masked interferon-alpha-2b) in combination with KEYTRUDA® for advanced melanoma.
2026 Clinical Program Milestones
CytomX is on track to deliver important clinical data for its product candidates in the coming year. Here are the key milestones related to CTMX's clinical programs:
- CX-2051 (Varsetatug Masetecan): Phase 1 colorectal cancer expansion data expected in Q1 2026.
- Combination Study: A Phase 1 study with bevacizumab starting in Q1 2026, with initial data anticipated by 1H 2027.
- CX-801 (Masked Interferon-alpha-2b): Initial combination data with KEYTRUDA® in melanoma is expected by the end of 2026.
- The company will present at the 44th Annual JP Morgan Healthcare Conference on January 14, 2026.
Leadership Insights on Clinical Progress
Dr. Sean McCarthy, CEO and Chairman of CytomX, expressed enthusiasm regarding the company’s progress: “We are excited to build on our transformational progress at CytomX with Varseta-M and will be focused on advancing this novel, potential first-in-class ADC towards a registrational study in late-line CRC.”
Dr. McCarthy emphasized the significance of the drug's design to target a broad, unselected CRC patient population, notably due to the consistent expression of EpCAM. He noted the promising initial clinical activity observed in the ongoing Phase 1 dose escalation studies.
Detailed Updates on Varseta-M and CX-801
Varseta-M (CX-2051) Developments
The ongoing Phase 1 expansions are exploring doses of 7.2 mg/kg, 8.6 mg/kg, and 10 mg/kg administered every three weeks. The trial is on track to enroll approximately 100 patients, with plans to align with the FDA regarding the study design for a potential registrational application in advanced CRC.
Progress on CX-801
The CX-801 study in advanced melanoma continues to demonstrate safety at increasing dose levels. The Phase 1 dose escalation for CX-801 in combination with KEYTRUDA® has also begun, with initial biomarker data supporting its mechanism presented at the 2025 SITC Annual Meeting.
About CytomX Therapeutics
CytomX is a clinical-stage, oncology-focused biopharmaceutical company aiming to develop innovative, conditionally activated biologics, designed to concentrate therapy within the tumor microenvironment. Through its proprietary PROBODY® platform, CytomX is committed to creating effective and safer cancer treatments.
The company's pipeline includes diverse therapeutic candidates from antibody-drug conjugates (ADCs) to T-cell engagers and immune modulators. Notable partnerships have been established with industry leaders such as Amgen, Astellas, Bristol Myers Squibb, Regeneron, and Moderna.
Forward-Looking Statements
This release includes forward-looking statements that involve risks and uncertainties, impacting the actual results and performance of CytomX and its collaborations. Investors are encouraged to refer to the statements regarding the future potential of CTMX's product candidates, including varsetatug masetecan and CX-801.