Press Releases April 30, 2026 08:00 AM

CytomX Therapeutics to Report First Quarter 2026 Financial Results on May 7, 2026

CytomX Therapeutics to announce Q1 2026 financial results on May 7, 2026, followed by webcast and conference call

By Avery Klein
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CTMX

CytomX Therapeutics, a clinical-stage biopharmaceutical company focused on developing conditionally activated biologics for cancer treatment, will report its Q1 2026 financial results after U.S. market close on May 7, 2026, and host a subsequent webcast and conference call. The company specializes in PROBODY therapeutics, with a pipeline including Varseta-M and CX-801 targeting metastatic cancers, and maintains collaborations with leading oncology firms.

CytomX Therapeutics to Report First Quarter 2026 Financial Results on May 7, 2026
CTMX
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Key Points

  • CytomX will release Q1 2026 financial results on May 7, 2026, with a follow-up webcast and conference call.
  • The company develops masked, conditionally activated biologics aiming to improve cancer therapy safety and effectiveness, including ADCs and cytokines.
  • CytomX has strategic collaborations with major oncology companies such as Amgen, Bristol Myers Squibb, Regeneron, and Moderna.

SOUTH SAN FRANCISCO, Calif., April 30, 2026 (GLOBE NEWSWIRE) -- CytomX Therapeutics, Inc. (Nasdaq: CTMX), a leader in the field of masked, conditionally activated biologics, today announced that it will report first quarter financial results on Thursday, May 7, 2026, after the close of U.S. markets. Following the announcement, the Company will host a conference call and webcast at 5:00 p.m. ET / 2:00 p.m. PT.

Participants may access the live webcast of the conference call from the Events and Presentations page of CytomX’s website at https://ir.cytomx.com/events-and-presentations. Participants may register for the conference call here and are advised to do so at least 10 minutes prior to joining the call. An archived replay of the webcast will be available on the Company’s website.

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, Bristol Myers Squibb, 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
cogden@cytomx.com

Investor Contact:
Precision AQ (formerly Stern Investor Relations)
Stephanie Ascher
stephanie.ascher@precisionaq.com

Media Contact:
Precision AQ
Colleen Ketchum
colleen.ketchum@precisionaq.com


Risks

  • As a clinical-stage biopharmaceutical company, CytomX’s product candidates are still under development and face risks of clinical trial failure or regulatory delays.
  • The success of conditionally activated PROBODY therapeutics in treating cancers is uncertain and depends on scientific and clinical advances.
  • Collaborations with partners may be subject to risks including changes in partner priorities or terms, which could impact development and commercialization.

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