A Phase 1 Basket Study Evaluating the Safety and Feasibility of T-Plex, Autologous Customized T Cell Receptor-Engineered T Cells Targeting Multiple Peptide/HLA Antigens in Participants With Antigen-positive Locally Advanced (Unresectable) or Metastatic Solid Tumors

Status: Recruiting
Location: See all (21) locations...
Intervention Type: Biological
Study Type: Interventional
Study Phase: Phase 1
SUMMARY

TScan Therapeutics is developing cellular therapies across multiple solid tumors in which autologous participant-derived engeneered T cells are engineered to express a T cell receptor that recognizes cancer-associated antigens presented on specific Human Leukocyte Antigen (HLA) molecules. This is a multi-center, non-randomized, multi-arm, open-label, basket study evaluating the safety and preliminary efficacy of single and repeat dose regimens of TCR'Ts as monotherapies and as T-Plex combinations after lymphodepleting chemotherapy in participants with locally advanced, metastatic solid tumors disease.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Must be at least 18 years.

• Locally advanced (unresectable) or metastatic solid tumor for which there are no available curative treatment options, after failure of the standard of care systemic therapies for that particular indication.

• Solid tumors, including but not limited to non-nasopharyngeal head and neck cancer, non-small cell lung cancer, cutaneous melanoma, cervical cancer, ovarian cancer, anal cancer and genital cancers. Other tumor types may be permitted if approved by TScan.

• Participants must express one of the following HLA types, as assessed by a qualified genomics assay in screening study TSCAN-003: HLA-B\*07:02, HLA-A\*01:01, HLA-C\*07:02 and/or HLA-A\*02:01

• Tumor must express one or more of the following: MAGE-A1, MAGE-A4, MAGE-C2, PRAME and HPV16 assessed in the last 8 months in screening study TSCAN-003 (NCT05812027).

• Eastern Cooperative Oncology Group (ECOG) Performance status 0-1 at screening.

• Participants must be able to understand and be willing to give informed consent; decision-impaired adults may consent with their legally authorized representative.

• At least 1 measurable lesion per modified Response Evaluation Criteria in Solid Tumors (RECIST) v1.1.

• Adequate bone marrow and organ function.

Locations
United States
Arizona
HonorHealth Research and Innovation Institute
RECRUITING
Scottsdale
California
University of California San Diego
RECRUITING
San Diego
Connecticut
Yale Cancer Center
RECRUITING
New Haven
Florida
Memorial Healthcare System
RECRUITING
Hollywood
University of Miami, Sylvester Comprehensive Cancer Center
RECRUITING
Miami
Orlando Health
RECRUITING
Orlando
University of South Florida
RECRUITING
Tampa
Illinois
University of Chicago
RECRUITING
Chicago
Kentucky
Norton Cancer Institute
RECRUITING
Louisville
Michigan
Karmanos Cancer Institute
RECRUITING
Detroit
Minnesota
University of Minnesota Masonic Cancer Center
RECRUITING
Minneapolis
North Carolina
University of North Carolina at Chapel Hill
RECRUITING
Chapel Hill
New York
Columbia University Herbert Irving Comprehensive Cancer Center
RECRUITING
New York
Ohio
Oncology Hematology Care
RECRUITING
Cincinnati
The Cleveland Clinic
RECRUITING
Cleveland
Oklahoma
OU Health Stephenson Cancer Center
RECRUITING
Oklahoma City
Oregon
Providence Cancer Institute Franz Clinic
RECRUITING
Portland
Pennsylvania
Allegheny Hospitals Network
RECRUITING
Pittsburgh
University of Pittsburgh Medical Center
RECRUITING
Pittsburgh
Tennessee
Sarah Cannon Research Institute
RECRUITING
Nashville
Texas
Baylor College of Medicine
RECRUITING
Houston
Contact Information
Primary
Erica Gagnon
medicalaffairs@tscan.com
857-399-9887
Backup
Kapadi CRO
kapadisites@kapadi.com
843-321-9429
Time Frame
Start Date: 2024-05-06
Estimated Completion Date: 2026-12-30
Participants
Target number of participants: 840
Treatments
Experimental: Monotherapy Cohort A
TSC-204-A0201
Experimental: Monotherapy Cohort B
TSC-204-C0702
Experimental: Monotherapy Cohort C
TSC-200-A0201
Experimental: T-Plex Combination Cohort A + B
TSC-204-A0201 and TSC-204-C0702
Experimental: T-Plex Combination Cohort B + C
TSC-204-C0702 and TSC-200-A0201
Experimental: T-Plex Combination Cohort A + C
TSC-204-A0201 and TSC-200-A0201
Experimental: Monotherapy Cohort D
TSC-203-A0201
Experimental: T-Plex Combination Cohort A + D
TSC-204-A0201 + TSC-203-A0201
Experimental: T-Plex Combination Cohort B + D
TSC-204-C0702 + TSC-203-A0201
Experimental: Monotherapy Cohort E
TSC-204-A0101
Experimental: Monotherapy Cohort F
TSC-201-B0702
Experimental: T-Plex Combination Cohort A + E
TSC-204-A0201 + TSC-204-A0101
Experimental: T-Plex Combination Cohort A + F
TSC-204-A0201 + TSC-201-B0702
Experimental: T-Plex Combination Cohort B + E
TSC-204-C0702 + TSC-204-A0101
Experimental: T-Plex Combination Cohort B + F
TSC-204-C0702 + TSC-201B0702
Experimental: T-Plex Combination Cohort C + D
TSC-200-A0201 + TSC-203-A0201
Experimental: T-Plex Combination Cohort C + E
TSC-200-A0201 + TSC-204-A0101
Experimental: T-Plex Combination Cohort C + F
TSC-200-A0201 + TSC-201B0702
Experimental: T-Plex Combination Cohort D + E
TSC-203-A0201 + TSC-204A0101
Experimental: T-Plex Combination Cohort D + F
TSC-203-A0201 + TSC-201B0702
Experimental: T-Plex Combination Cohort E + F
TSC-204-A0101 + TSC-201-B0702
Experimental: Monotherapy Cohort G
TSC-202-A0201
Experimental: T-Plex Combination Cohort A + G
TSC-204-A0201 + TSC-202-A0201
Experimental: T-Plex Combination Cohort B + G
TSC-204-C0702 + TSC-202-A0201
Experimental: T-Plex Combination Cohort C+ G
TSC-200-A0201 + TSC-202-A0201
Experimental: T-Plex Combination Cohort D + G
TSC-203-A0201 + TSC-202-A0201
Experimental: T-Plex Combination Cohort E + G
TSC-204-A0101 + TSC-202-A0201
Experimental: T-Plex Combination Cohort F + G
TSC-201-B0702 + TSC-202-A0201
Sponsors
Leads: TScan Therapeutics, Inc.

This content was sourced from clinicaltrials.gov

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