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A Basket Study of Customized Autologous TCR-T Cell Therapies in Patients With Locally Advanced (Unresectable) or Metastatic Solid Tumors

← catalyst calendar

NCT05973487 · readout in 133 d

Sponsored by TScan Therapeutics, Inc. (industry) · TCRX — their whole pipeline →.

Phase
Phase 1
Status
Active, not recruiting
Study type
Interventional
Design
Non randomized · None · Treatment
Enrollment
840estimated
Sites
21
Country
United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2024-05-06actualWhen the study began enrolling
Primary completion2026-12-30estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2026-12-30estimatedThe whole study's end, after follow-up
First posted2023-08-03actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-11-17actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Head and Neck Cancer
  • Cervical Cancer
  • Non-small Cell Carcinoma
  • Melanoma
  • Ovarian Cancer
  • Anogenital Cancers
  • HPV - Anogenital Human Papilloma Virus Infection
  • HPV-Related Cervical Carcinoma
  • HPV-Related Carcinoma
  • HPV-Related Squamous Cell Carcinoma
  • HPV-Related Malignancy
  • HPV-Related Adenocarcinoma
  • HPV Positive Oropharyngeal Squamous Cell Carcinoma
  • HPV-Related Adenosquamous Carcinoma
  • HPV-Associated Vaginal Adenocarcinoma
  • HPV-Related Endocervical Adenocarcinoma
  • HPV-Related Anal Squamous Cell Carcinoma
  • HPV-Related Verrucous Carcinoma
  • HPV-Related Penile Squamous Cell Carcinoma
  • HPV-Related Vulvar Squamous Cell Carcinoma
  • HPV Positive Rectal Squamous Cell Carcinoma

Interventions

  • Biological: TSC-204-A0201
  • Biological: TSC-204-C0702
  • Biological: TSC-200-A0201
  • Biological: TSC-204-A0201 + TSC-204-C0702
  • Biological: TSC-204-A0201 + TSC-200-A0201
  • Biological: TSC-204-C0702 + TSC-200-A0201
  • Biological: TSC-204-A0201 + TSC-203-A0201
  • Biological: TSC-204-C0702 + TSC-203-A0201
  • Biological: TSC-200-A0201 + TSC-203-A0201
  • Biological: TSC-203-A0201
  • Biological: TSC-204-A0101
  • Biological: TSC-201-B0702
  • Biological: TSC-204-A0201 + TSC-204-A0101
  • Biological: TSC-204-A0201 + TSC-201-B0702
  • Biological: TSC-204-C0702 + TSC-204-A0101
  • Biological: TSC-204-C0702 + TSC-201-B0702
  • Biological: TSC-200-A0201 + TSC-204-A0101
  • Biological: TSC-200-A0201 + TSC-201-B0702
  • Biological: TSC-203-A0201 + TSC-204-A0101
  • Biological: TSC-203-A0201 + TSC-201-B0702
  • Biological: TSC-202-A0201
  • Biological: TSC-204-A0201 + TSC-202-A0201
  • Biological: TSC-204-C0702 + TSC-202-A0201
  • Biological: TSC-200-A0201 + TSC-202-A0201
  • Biological: TSC-203-A0201 + TSC-202-A0201
  • Biological: TSC-204-A0101 + TSC-202-A0201
  • Biological: TSC-201-B0702 + TSC-202-A0201

Primary outcomes

what the primary-completion date above is the date OF
Evaluate the safety of monotherapy and T- Plex combination TCR-Ts
measured 28 days
Determine the recommended phase 2 dose of monotherapy and T- Plex combination TCR-Ts
measured Up to 12 months

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