A Phase I Feasibility And Safety Study of Fluorescein-Specific (FITC-E2) CAR T Cells In Combination With Parenterally Administered Folate-Fluorescein (UB-TT170) For Osteogenic Sarcoma

A Phase I Feasibility And Safety Study of Fluorescein-Specific (FITC-Ew) CAR T Cells In Combination With Parenterally Administered Folate-Fluorescein (UB-TT170) For Osteogenic Sarcoma

The purpose of this study is to see if a new treatment could help patients who have osteosarcoma that does not go away with treatment (is refractory) or comes back after treatment (is recurrent).This study is testing a combination of study therapies, UB-TT170 and genetically modified chimeric antigen receptor T lymphocyte (CAR T) cells, which work together in a way that is different from chemotherapy.

In this study, researchers will take some of your blood and remove the T cells in a process called "apheresis". Then the T cells are taken to a lab and changed to CAR T cells that recognize the flags from UB-TT170. Once researchers think they have grown enough CAR T cells, called antiFL(FITC-E2) CAR T cells, to fight your cancer, you may get some chemotherapy to make room in your body for the new cells and then have those cells put back in your body.

A few days after the you get your CAR T cell infusion you will start to get infusions of UB-TT170, with the dose slowly increasing for the first few infusions until you have reached a maximum dose that you will get on a regular schedule. The UB-TT170 will attach to your tumor cells and flag them so that they attract the CAR T cells. When the CAR T cells see the labeled tumor cells they can kill the tumor cells.

The active part of the study lasts about 8 months, and if you get the CAR T cell infusion you will be in long-term follow-up for 15 years.

Study Overview

• Status: Active, not recruiting
• Conditions: Osteosarcoma
• Intervention / Treatment: Biological: SCRI-E2CAR_EGFRtv1; Drug: UB_TT170

• Study Type: Interventional
• Enrollment (Estimated): 21
• Phase: Phase 1

Contacts and Locations

Study Locations

• United States
  • Washington
    • Seattle, Washington, United States, 98105
      • Seattle Children's Hospital

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 11 years to 26 years (Child, Adult)
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

• Refractory or recurrent/progressive osteosarcoma that has failed first line therapy for Osteosarcoma per NCCN or upfront Children's Oncology Group clinical trial and is not amenable to surgical resection (must meet one of the following):

  1. New site of measurable disease by radiographic imaging or histologic confirmation
  2. New site of evaluable disease by radiographic imaging (including FDG-PET) or histologic confirmation
  3. Greater than 20% increase in at least one tumor dimension documented by CT/MRI, AND a maximum absolute increase of 5 mm in longest dimension of existing lesion(s) (previously irradiated lesions may be included)
  4. Persistent measurable disease or FDG-PET avid bone metastasis that has failed to achieve complete remission to upfront conventional therapy (surgery, radiotherapy and/or chemotherapy)
• Able to tolerate apheresis, including placement of temporary apheresis catheter, if necessary, or already has an apheresis product available for use in manufacturing
• Life expectancy ≥ 8 weeks
• Lansky or Karnofsky score ≥ 50
• Anti-cancer agents, radiotherapy, cytoxic chemotherapy, biologic therapy, anti-tumor antibody therapy, genetically modified cell therapy, and, if no apheresis product available, corticosteroid therapy (excluding physiologic replacement), discontinued within protocol specified wash-out period
• Adequate hematologic, renal, hepatic, cardiac, and respiratory function.
• Negative HIV, hepatitis B and C test within 3 months
• If of child-bearing or fathering potential, willing to use highly effective contraception through 12 months following final stud drug infusion

Exclusion Criteria:

• Active malignancy other than primary malignant solid tumor diagnosis (CNS intracranial metastases are allowed)
• Ongoing, symptomatic CNS pathology requiring medical intervention
• Receiving external beam radiotherapy
• Presence of active, severe infection
• Primary immunodeficiency syndrome
• Pregnant or breast feeding
• Unwilling to provide consent/assent for study participation, including 15 year follow up
• Presence of any condition that, in the opinion of the investigator, would prohibit the subject from undergoing treatment under this protocol.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: UB-TT170 following SCRI-E2CAR_EGFrtv1; Following CAR T cell administration, subjects will receive a first Course of 3 escalating doses of UB-TT170 over 2 weeks followed by fixed weekly dosing for 2 weeks. If eligible, subjects may proceed to Courses 2 - 4 consisting of 7 weekly doses of UB-TT170.	Biological: SCRI-E2CAR_EGFRtv1; Autologous CD4+ and CD8+ T cells that have been genetically modified to express antiFL(FITC-E2); Drug: UB_TT170; Bispecific small molecule adapter formulated with phosphate buffered saline

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Adverse events associated with ex-vivo expanded autologous T cells genetically modified to express an antiFL(FITC-E2) CAR administered with UB-TT170 will be assessed	The type, frequency, severity, and duration of adverse events will be summarized	30 days

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Ability to manufacture antiFL(FITC-E2) CAR cells	The number of successfully manufactured antiFL(FITC-E2) CAR products will be assessed	28 Days
Evaluate the pharmacokinetics of UB-TT170 in combination with the anti-FL(FITC-E2) CAR T cells	Pharmacokinetics of UB-TT170 in combination with the anti-FL(FITC-E2) CAR T cells	25 days

Collaborators and Investigators

• Sponsor: Seattle Children's Hospital
• Collaborators: Umoja Biopharma
• Investigators: Principal Investigator: Catherine Albert, MD, Seattle Children's Hospital

Study record dates

Study Major Dates

• Study Start (Actual): May 20, 2022
• Primary Completion (Actual): March 12, 2025
• Study Completion (Estimated): May 1, 2040

Study Registration Dates

• First Submitted: March 20, 2019
• First Submitted That Met QC Criteria: March 28, 2022
• First Posted (Actual): April 5, 2022

Study Record Updates

• Last Update Posted (Actual): November 20, 2025
• Last Update Submitted That Met QC Criteria: November 17, 2025
• Last Verified: October 1, 2025

More Information

Terms related to this study

• Keywords: osteosarcoma; bone cancer; pediatric sarcoma; young adult sarcoma
• Additional Relevant MeSH Terms: Bone Diseases; Musculoskeletal Diseases; Neoplasms by Site; Neoplasms; Neoplasms by Histologic Type; Sarcoma; Neoplasms, Connective and Soft Tissue; Neoplasms, Bone Tissue; Neoplasms, Connective Tissue; Osteosarcoma; Bone Neoplasms
• Other Study ID Numbers: ENLIGHTen-01

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: Yes
• Studies a U.S. FDA-regulated device product: No
• product manufactured in and exported from the U.S.: No