Immune System to Work Against Disease
About Our Approach
We use a patient’s own cells to manufacture a personalized therapy. After blood collection, we isolate target cell types, use our SQZ® technology to engineer their functions and administer them back to the patient. This manufacturing process typically takes less than 24hrs and a patient can receive their first dose about a week after blood collection. Once administered, SQZ® engineered cells are designed to home to specialized immune structures, such as the lymph nodes and spleen, and direct the patient’s immune system to target disease.
Our clinical programs are in oncology for the treatment of HPV16 positive cancers.
The Patient Experience
No lengthy hospital stays
Time to treatment: ~1 week
Administration is a simple syringe push
Patients and their physicians can expect rapid answers to questions about our clinical trial. Your time is important, and we will endeavor to respond with urgency.
Current Active Enrollment · Oncology
SQZ Biotech is actively enrolling in the following trials for patients with HPV16+ cancers with multiple sites in the United States.
Enrolling HPV+ Cancers
- Head and Neck
- Male or Female 18 years of age or older
- Histologically confirmed incurable or metastatic solid tumors that are HPV16+
- Cancer progression after at least one available standard therapy for incurable disease, or patient is intolerant to or refuses standard therapy(ies) or has a tumor for which no standard therapy(ies) exist
COMMANDER-001 · PHASE 1/2 CLINICAL TRIAL
Enhanced APC (eAPC) therapeutic candidate derived from patient’s own white blood cells
- Designed to leverage the advantages and functionalities of five different mRNAs squeezed into white blood cells
- Administered as monotherapy or in combination with checkpoint inhibitor pembrolizumab
- In preclinical studies, SQZ® eAPCs have been shown to generate robust CD8 T cell responses against multiple antigens, through simultaneous expression of antigens, CD86, membrane bound IL-2, and membrane bound IL-12
SQZ-AAC-HPV-101 · PHASE 1/2 CLINICAL TRIAL
AAC therapeutic candidate derived from patient’s own red blood cells
- Designed to transport tumor-specific antigen and activating adjuvant to a patient’s own antigen presenting cells in vivo
- Administered as a monotherapy or in combination with checkpoint inhibitors ipilimumab or nivolumab
- In preclinical studies, SQZ® AACs have demonstrated robust immune responses, CD8 T cell infiltration, and correlated tumor reduction
Expanded Access Policy
In expanded access programs, patients with serious diseases or life-threatening conditions who have exhausted all available options and do not meet the eligibility criteria to participate in a clinical trial may be able to access investigational therapies. At this time in our clinical development path, however, we do not offer expanded access as we believe that enrollment in our clinical trial is the best way for us to develop safe and effective treatments that would ultimately benefit a larger number of patients.
We encourage all patients and physicians who are interested in accessing our investigational therapy to contact us for information. You can also visit trial and enrollment details and see additional details on clinicaltrials.gov
COMMANDER-001 ENROLLING SITES
- HonorHealth, Scottsdale, AZ
- University of Colorado, Aurora, CO
- Tennessee Oncology, Nashville, TN
- University of Cincinnati, Cincinnati, OH
- Massachusetts General Hospital, Boston, MA
- More sites expected to open soon!
SQZ-AAC-HPV-101 ENROLLING SITES
- City of Hope Medical Center, CA
- Barbara Ann Karmanos Cancer Institute, MI
- Roswell Park Comprehensive Cancer Center, NY
- Icahn School of Medicine at Mount Sinai, NY
- Oregon Health & Science University, OR
We are committed to advancing the clinical development of cell therapies that are safe, effective and accessible to patients worldwide. We are actively engaged with leading advocacy organizations working to support patients and their families living with cancer. For additional information on HPV+ cancers, the following organizations can provide educational and other resources.
We are not responsible for content provided by these organizations.