Phase I Study of Radiolabeled OTSA101-DTPA in Patients With Relapsed or Refractory Synovial Sarcoma

Last updated: January 31, 2024
Sponsor: OncoTherapy Science, Inc.
Overall Status: Terminated

Phase

1

Condition

Sarcoma

Treatment

OTSA101-DTPA-111In

OTSA101-DTPA-90Y

Clinical Study ID

NCT04176016
OTS3050102
  • Ages > 18
  • All Genders

Study Summary

The purpose of this study is to evaluate safety and pharmacokinetics as well as the biodistribution of OTSA101-DTPA-111In and to evaluate the safety of intravenous administration of OTSA101-DTPA-90Y.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Patients with a documented relapsed or refractory synovial sarcoma after standardchemotherapy
  2. Patients ≥18 years of age at the time of obtaining informed consent
  3. Patients with an Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0 or 1
  4. Patients with measurable lesion
  5. Patients not received any anti-malignancy agent or specified surgical interventionwithin 28 days or specified radiotherapy within 14 days prior to study registration.
  6. Patients without any clinically significant laboratory abnormality.
  7. Patients with adequate heart function as measured by echocardiography or multiplegated acquisition scan (MUGA).
  8. Patients with adequate pulmonary function as measured by pulmonary function tests.
  9. Patients who are either not of childbearing potential or who agree to use acontraception method during the study and for 12 months after the last dose of studydrug
  10. Patients must be able to understand and be willing to sign a written informed consent

Exclusion

Exclusion Criteria:

  1. Patients with documented concurrent malignancy.
  2. Patients with brain metastasis with clinical symptoms.
  3. Patients with any infection requiring systemic treatment.
  4. Patients with lung inflammation or pulmonary fibrosis.
  5. Patients with a known history of hypersensitivities to antibody agents or serumalbumin agents.
  6. Patients with a known history of autoimmune diseases.
  7. Patients with myocardial infarction (MI) within 6 months prior to study registration.
  8. Patients with uncontrolled diseases.
  9. Patients with any disease requiring continuous systemic administration of steroids orimmunosuppressants.
  10. Patients with evidence of active HBV, HCV or HIV infection.
  11. Pregnant or breastfeeding female patients, or female patients with suspectedpregnancy.
  12. Patients who are participating any other investigational treatments during the study.
  13. Patients with psychiatric disorders and is considered to have difficulty to studyparticipation.

Study Design

Total Participants: 12
Treatment Group(s): 2
Primary Treatment: OTSA101-DTPA-111In
Phase: 1
Study Start date:
January 10, 2020
Estimated Completion Date:
January 11, 2024

Connect with a study center

  • Osaka International Cancer Institute

    Osaka,
    Japan

    Site Not Available

  • Cancer Institute Hospital of JFCR

    Tokyo,
    Japan

    Site Not Available

  • National Cancer Center Hospital

    Tokyo,
    Japan

    Site Not Available

Not the study for you?

Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.