Teclison

Teclison

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Private Company

Total funding raised: $12.5M

Overview

Teclison is a private, pre-revenue biotech founded in 2015 and based in San Diego, CA. The company is advancing a novel therapeutic platform that combines tumor-hypoxia-inducing procedures with immune system activation to treat solid tumors, with a lead program (TEC-001) in Phase 2 trials for various cancers including hepatocellular carcinoma (HCC). Teclison has a strategic collaboration with Merck and is targeting a significant unmet need in patients who respond poorly to current immunotherapies.

Oncology

Technology Platform

A platform designed to remodel the tumor immune microenvironment by inducing controlled tumor hypoxia. This triggers tumor necrosis and the release of antigens, which primes a systemic anticancer immune response, particularly to enhance the efficacy of immune checkpoint inhibitors.

Funding History

2
Total raised:$12.5M
Series A$12M
Grant$500K

Opportunities

Teclison addresses the large unmet need in patients with solid tumors, especially liver metastases, who are resistant to current immunotherapies.
Its platform, if successful, could become a foundational combination partner for blockbuster checkpoint inhibitors across multiple major cancer indications.
The strategic collaboration with Merck provides validation and critical resources for development.

Risk Factors

The company faces high clinical development risk, as its novel approach must prove effective in ongoing trials.
It is dependent on partners for combination drugs and substantial future financing.
Intense competition in the immuno-oncology space from larger, well-funded entities poses a significant challenge.

Competitive Landscape

Teclison competes in the crowded immuno-oncology combination therapy arena, facing numerous companies developing next-gen cytokines, cancer vaccines, oncolytic viruses, and other TME modulators. Its differentiation lies in its specific hypoxia-inducing mechanism to prime immunity, but it must demonstrate superior clinical efficacy to established and emerging combination regimens.