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
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Patients with a documented relapsed or refractory synovial sarcoma after standardchemotherapy
- Patients ≥18 years of age at the time of obtaining informed consent
- Patients with an Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0 or 1
- Patients with measurable lesion
- Patients not received any anti-malignancy agent or specified surgical interventionwithin 28 days or specified radiotherapy within 14 days prior to study registration.
- Patients without any clinically significant laboratory abnormality.
- Patients with adequate heart function as measured by echocardiography or multiplegated acquisition scan (MUGA).
- Patients with adequate pulmonary function as measured by pulmonary function tests.
- 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
- Patients must be able to understand and be willing to sign a written informed consent
Exclusion
Exclusion Criteria:
- Patients with documented concurrent malignancy.
- Patients with brain metastasis with clinical symptoms.
- Patients with any infection requiring systemic treatment.
- Patients with lung inflammation or pulmonary fibrosis.
- Patients with a known history of hypersensitivities to antibody agents or serumalbumin agents.
- Patients with a known history of autoimmune diseases.
- Patients with myocardial infarction (MI) within 6 months prior to study registration.
- Patients with uncontrolled diseases.
- Patients with any disease requiring continuous systemic administration of steroids orimmunosuppressants.
- Patients with evidence of active HBV, HCV or HIV infection.
- Pregnant or breastfeeding female patients, or female patients with suspectedpregnancy.
- Patients who are participating any other investigational treatments during the study.
- 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,
JapanSite Not Available
Cancer Institute Hospital of JFCR
Tokyo,
JapanSite Not Available
National Cancer Center Hospital
Tokyo,
JapanSite Not Available
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