Press Releases May 21, 2026 08:00 AM

CytomX Therapeutics to Present at Upcoming June Investor Conferences

CytomX Therapeutics to Participate in Major June Investor Conferences to Highlight Oncology Pipeline

By Nina Shah CTMX

CytomX Therapeutics announced its participation in the upcoming Jefferies Global Healthcare Conference and Goldman Sachs 47th Annual Global Healthcare Conference in June 2026. The clinical-stage biopharmaceutical company will showcase its novel PROBODY therapeutics focused on localized cancer treatments, including candidates Varseta-M and CX-801. Management will also hold one-on-one investor meetings and provide live webcasts of presentations.

CytomX Therapeutics to Present at Upcoming June Investor Conferences
CTMX

Key Points

  • CytomX will present at two major June healthcare investor conferences, providing updates to investors and analysts.
  • The company focuses on masked, conditionally activated biologics with a pipeline addressing multiple cancer treatment modalities, including antibody-drug conjugates and cytokines.
  • Strategic collaborations with leading oncology companies like Amgen, Regeneron, and Moderna support CytomX's development efforts.

SOUTH SAN FRANCISCO, Calif., May 21, 2026 (GLOBE NEWSWIRE) -- CytomX Therapeutics, Inc. (Nasdaq: CTMX), a leader in the field of masked, conditionally activated biologics, today announced that management will participate in the following investor conferences in June.

Jefferies Global Healthcare Conference
Date: Thursday, June 4, 2026
Fireside Chat: 3:10 p.m. ET
Location: New York, NY

Goldman Sachs 47th Annual Global Healthcare Conference
Date: Wednesday, June 10, 2026
Fireside Chat: 9:20 a.m. ET
Location: Miami, FL

A live webcast of the presentation will be available on the Events and Presentations page of CytomX’s website at www.cytomx.com. In addition, management will be available for one-on-one meetings with investors who are registered to attend the conferences.

About CytomX Therapeutics, Inc.

CytomX is a clinical-stage, oncology-focused biopharmaceutical company focused on developing novel conditionally activated, masked PROBODY® therapeutics designed to be localized to the tumor microenvironment. By pioneering a novel pipeline of localized biologics, powered by its PROBODY therapeutic platform, CytomX’s vision is to create safer, more effective therapies for the treatment of cancer. CytomX’s robust and differentiated pipeline comprises therapeutic candidates across multiple treatment modalities including antibody-drug conjugates (“ADCs”), cytokines and T-cell engagers. CytomX’s clinical-stage pipeline includes varsetatug masetecan (Varseta-M; CX-2051) and CX-801. Varseta-M is a masked, conditionally activated ADC armed with a topoisomerase-1 inhibitor payload and directed toward epithelial cell adhesion molecule (EpCAM). EpCAM is a highly expressed tumor antigen that has previously been undruggable due to expression on normal tissues. Varseta-M is designed to open a therapeutic window for this high potential target and is initially being developed for the treatment of metastatic colorectal cancer. Varseta-M was discovered in collaboration with ImmunoGen, now part of AbbVie. CX-801 is a masked interferon alpha-2b PROBODY® cytokine with broad potential applicability in traditionally immuno-oncology sensitive as well as insensitive (cold) tumors. CX-801 is initially being developed for the treatment of metastatic melanoma. CytomX has established strategic collaborations with multiple leaders in oncology, including Amgen, Regeneron and Moderna. For more information about CytomX and how it is working to make conditionally activated treatments the new standard-of-care in the fight against cancer, visit www.cytomx.com and follow us on LinkedIn and X (formerly Twitter).

Company Contact:
Chris Ogden
SVP, Chief Financial Officer
[email protected]

Investor Contact:
Precision AQ
Stephanie Ascher
[email protected]

Media Contact:
Precision AQ
Colleen Ketchum
[email protected]


Risks

  • Clinical-stage drug candidates such as Varseta-M and CX-801 face typical development and regulatory risks that could delay or alter outcomes impacting the oncology and biopharmaceutical sectors.
  • Dependence on continued strategic partnerships and collaborations, which if reduced or lost, may affect development pipelines and commercialization potential.
  • Market and investor reception to presentations could be muted if no new substantive clinical or regulatory progress is disclosed.

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