Cartherics to present CTH-401 ovarian cancer data at SITC 2026
Cartherics will present new CTH-401 data at the Society for Immunotherapy of Cancer 2026 Annual Meeting in Phoenix, with an oral talk and poster on its off-the-shelf iPSC-derived CAR-NK therapy for ovarian cancer. The company says IND-enabling studies are complete and a first-in-human trial is planned for early 2027, pending regulatory approval.
Why it matters: - Ovarian cancer causes more than 200,000 deaths worldwide each year. - Most patients are diagnosed at an advanced stage. - Fewer than 30% of patients survive five years. - CTH-401 is designed as an off-the-shelf immune cell therapy, which could avoid the need to custom-make treatment for each patient. - Cartherics is aiming to bring the program into the clinic in early 2027, subject to regulatory approval.
What happened: - Cartherics said it will present an update on CTH-401 at the Society for Immunotherapy of Cancer 2026 Annual Meeting in Phoenix, Arizona. - Deputy Chief Scientific Officer Dr. Keefe Chan will deliver an oral presentation and a poster. - The oral presentation is scheduled for Oral Abstract Session 2 on Friday, Nov. 6, from 3:58 p.m. to 4:13 p.m. Mountain Time. - The poster number is 161. - The presentation title is “CTH-401: Allogeneic iPSC-derived CAR-NK cells for the treatment of ovarian cancer.”
The details: - CTH-401 is made from induced pluripotent stem cells, or iPSCs. - The therapy is engineered to target TAG-72, a protein found on ovarian and other adenocarcinomas with negligible expression on normal adult tissues. - The cells include two gene deletions, DGKα and DGKζ, which remove an internal brake that normally dampens natural killer cell function after activation. - Cartherics manufactures CTH-401 in its own clinical manufacturing facility in Melbourne. - The product is made in advance from a master cell bank. - The company says the therapy is designed to be manufactured at scale and delivered off the shelf, unlike autologous cell therapies made for each patient. - Key findings for the presentation include high-consistency production from a fully characterised, GMP-compliant master cell bank. - Laboratory studies showed CTH-401 killed TAG-72-positive cancer cells. - The gene deletions significantly improved resistance to tumour immunosuppression. - CTH-401 produced significant tumour control in a preclinical ovarian cancer model. - GLP toxicology studies showed an acceptable safety profile at dose equivalents well above the intended clinical range. - IND-enabling studies are complete. - Read the abstract published in the Journal for ImmunoTherapy of Cancer.
Between the lines: - The presentation positions Cartherics as moving from preclinical development toward first-in-human testing. - In-house discovery, process development and manufacturing may give the company more control over quality, cost and timelines. - TAG-72 expression in colorectal, gastric and other adenocarcinomas suggests a possible path beyond ovarian cancer. - The company’s iPSC platform is also intended to support additional programs, including endometriosis. - Dr. Chan said the work reflects years of development, from gene editing iPSCs to building a scalable manufacturing process for an off-the-shelf iPSC-derived natural killer cell product.
What's next: - Cartherics plans a first-in-human ovarian cancer trial for early 2027, pending regulatory approval. - The company may expand CTH-401 into other solid tumors if future data support broader use. - Additional product programs from the iPSC platform could follow, including work in endometriosis.
The bottom line: - Cartherics is using SITC 2026 to showcase a lead ovarian cancer cell therapy that is preclinical, manufacturable at scale and nearing the clinic.
Disclaimer: This article was produced by AGP Wire with the assistance of artificial intelligence based on original source content and has been refined to improve clarity, structure, and readability. This content is provided on an “as is” basis. While care has been taken in its preparation, it may contain inaccuracies or omissions, and readers should consult the original source and independently verify key information where appropriate. This content is for informational purposes only and does not constitute legal, financial, investment, or other professional advice.
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