Nivolumab (Opdivo®) Plus ABI-009 (Nab-rapamycin) for Advanced Sarcoma
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|ClinicalTrials.gov Identifier: NCT03190174|
Recruitment Status : Recruiting
First Posted : June 16, 2017
Last Update Posted : September 6, 2018
|Condition or disease||Intervention/treatment||Phase|
|Undifferentiated Pleomorphic Sarcoma Liposarcoma Chondrosarcoma Osteosarcoma Ewing Sarcoma||Drug: Nab-Rapamycin Biological: Nivolumab||Phase 1 Phase 2|
The primary objective of this study is to investigate the maximum tolerated dose of ABI-009, an mTOR inhibitor, when given sequentially with nivolumab in advanced UPS, LPS, CS, OS and Ewing sarcoma.
The secondary objectives are to investigate the disease control rate (DCR) and progression free survival (PFS) using nivolumab/ABI-009 combination therapy in advanced UPS, LPS, CS, OS and Ewing sarcoma.
The exploratory objectives are (1) To correlate progression free survival (PFS) based on Immune-related Response Criteria (irRECIST) with that based on RECIST v1.1, and (2) To correlate PFS with PD-1 and PD-L1 expression in patients' tumors.
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||40 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||A Phase 1b Single Center Investigation of Safety/Efficacy of Nivolumab (Opdivo®) and ABI-009 (Nab-rapamycin) in Patients With Advanced Undifferentiated Pleomorphic Sarcoma, Liposarcoma, Chondrosarcoma, Osteosarcoma and Ewing Sarcoma|
|Actual Study Start Date :||August 24, 2017|
|Estimated Primary Completion Date :||February 1, 2020|
|Estimated Study Completion Date :||April 1, 2020|
Experimental: Arm 1
This is an open label, dose-seeking phase 1b study using a defined dose of nivolumab and escalating doses of Nab-Rapamycin (ABI-009) given intravenously.
I. Dose Escalation Phase 1 Part of Study: The study will employ the standard "cohort of three" design. No intra-patient dose escalation will take place.
II. Expansion Phase 1b Part of Study: Following dose escalation, an additional 22-28 patients will receive ABI-009 at the MTD and defined doses of nivolumab to assess overall safety and potential efficacy in a greater number of patients. Patients in the expansion phase of the study may continue treatment up to 18 three-week cycles or until significant disease progression or unacceptable toxicity occurs.
Escalating doses of ABI-009 will be given IV over 30 min for 2 of every 3 weeks beginning Day 8 Cycle 2. Only nivolumab will be given in Cycle 1. At Dose Level 1, 3-6 patients will receive 56 mg/m2; at Dose Level 2, 3-6 six patients will receive 75 mg/m2; and at Dose Level 3, 3-6 patients will receive 100 mg/m2.
Other Name: ABI-009
A defined dose of nivolumab, 3 mg/kg, will be given IV over 30 minutes q 3 weeks
Other Name: Opdivo
- Maximum tolerated dose [ Time Frame: 6 months ]Dose escalation study, determination of maximum tolerated dose (MTD) in previously treated patients with soft tissue sarcoma
- Disease control rate [ Time Frame: 24 months ]Effect of dual therapy with ABI-009 and nivolumab on Disease Control Rate in advanced soft tissue sarcoma
- Progression free survival [ Time Frame: 24 months ]Effect of dual therapy with ABI-009 and nivolumab on progression free survival (PFS)
- Overall survival [ Time Frame: 24 months ]Effect of dual therapy with ABI-009 and nivolumab on overall survival in advanced soft tissue sarcoma
- Disease control rate and PD-L1 expression in tumors [ Time Frame: 30 months ]Correlation between disease control rate and PD-L1 expression in patients' tumors
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03190174
|Contact: Erlinda M Gordon, MDemail@example.com|
|Contact: Victoria Chua-Alcalafirstname.lastname@example.org|
|United States, California|
|Sarcoma Oncology Research Center||Recruiting|
|Santa Monica, California, United States, 90403|
|Contact: Erlinda M Gordon, MD 310-552-9999 email@example.com|
|Contact: Victoria Chua-Alcala 310-552-9999 firstname.lastname@example.org|
|Principal Investigator: Erlinda M Gordon, MD|
|Sub-Investigator: Sant P Chawla, MD|
|Sub-Investigator: Kamalesh K Sankhala, MD|
|Sub-Investigator: Doris Quon, MD|
|Principal Investigator:||Erlinda M Gordon, MD||Sarcoma Oncology Research Center|