Adoptive Immunotherapy for Advanced MUC1* Positive Breast Cancer With Autologous T Cells Engineered to Express a Chimeric Antigen Receptor, huMNC2-CAR44 or huMNC2-CAR22, Specific for a Cleaved Form of MUC1 (MUC1*)
Minerva Biotechnologies Corporation is advancing a novel adoptive immunotherapy approach for advanced MUC1* positive breast cancer using autologous T cells engineered to express either huMNC2-CAR44 or huMNC2-CAR22. This therapy targets a specific form of MUC1, which is prevalent in various solid tumors, including breast cancer. The market for breast cancer therapies is substantial, with a growing demand for innovative treatments, particularly in advanced stages where current therapies often yield limited efficacy. The competitive landscape includes established players in CAR-T therapies and emerging biotech firms focusing on similar targets. Successful outcomes in this trial could position Minerva favorably within this competitive environment, potentially leading to partnerships or acquisition interest. Diligence should focus on the safety profile and the ability to demonstrate significant clinical efficacy compared to existing therapies.
Indication: Metastatic Breast Cancer
Modality: protein therapy
Target: Chimeric Antigen Receptor (CAR) targeting the cleaved form of MUC1 (MUC1*)
Sponsor: Minerva Biotechnologies Corporation
Source URL: ClinicalTrials.gov
Source updated: Detailed source ingestion pending
Ingested: Jun 23, 2026
Model: trialsignal-ai-v1
Validation: validated
Matched by target_normalized: Chimeric Antigen Receptor (CAR) targeting the cleaved form of MUC1 (MUC1*)
View original source fields
Condition raw: Metastatic Breast Cancer
Condition normalized: Metastatic Breast Cancer
Modality raw: protein therapy
Modality normalized: protein therapy
Target raw: Chimeric Antigen Receptor (CAR) targeting the cleaved form of MUC1 (MUC1*)
Target normalized: Chimeric Antigen Receptor (CAR) targeting the cleaved form of MUC1 (MUC1*)