STAb Therapeutics

STAb Therapeutics

Barcelona, Spain· Est.
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Private Company

Total funding raised: $14.5M

Overview

STAb Therapeutics, a 2018 spin-off from the Research Institute Hospital 12 de Octubre (imas12), is pioneering a novel T cell redirecting immunotherapy. Its STAb platform engineers T cells to secrete T cell engagers (TCEs) in vivo, aiming to enhance anti-tumor responses through sustained drug levels and recruitment of bystander T cells. The company is advancing its lead candidate, STAb-T19 for B-cell malignancies, towards clinical trials, supported by non-dilutive grants from Spanish public entities. It operates as a private, preclinical-stage biotech based in Madrid.

OncologyHematological Malignancies

Technology Platform

STAb (Secreting T-cell Adoptive therapy) platform: A hybrid immunotherapy that engineers patient T cells to secrete T cell engager (TCE) antibodies in vivo, combining principles of adoptive cell therapy and bispecific antibodies.

Funding History

2
Total raised:$14.5M
Series A$12M
Seed$2.5M

Opportunities

The STAb platform addresses key limitations of existing cell therapies and bispecific antibodies by enabling sustained, in vivo drug production and polyclonal T cell recruitment.
Success with the lead CD19 program could validate the platform for rapid expansion into other hematological and solid tumor targets, tapping into multi-billion dollar oncology markets.

Risk Factors

The novel, unproven technology carries high clinical risk regarding safety and efficacy in humans.
As a pre-revenue, early-stage company, securing sufficient funding for costly clinical trials is a major hurdle.
It also faces intense competition in the crowded CD19-targeted therapy landscape.

Competitive Landscape

STAb Therapeutics competes in the advanced therapy space against approved CD19 CAR-T products (e.g., Novartis's Kymriah, Gilead's Yescarta) and bispecific antibodies (e.g., Amgen's Blincyto). Its differentiation strategy is based on its hybrid platform's potential for improved persistence, broader T cell recruitment, and sustained pharmacokinetics compared to these established modalities.