A Phase I/II Study of Intratumoral Injection of SD-101
Part of paid clinical trials in Stanford, California.
- Sponsor
- Robert Lowsky
- Study ID
- NCT02254772
- Phase
- PHASE1/PHASE2
- Status
- Completed
Conditions
- Extranodal Marginal Zone B-cell Lymphoma of Mucosa-associated Lymphoid Tissue
- Nodal Marginal Zone B-cell Lymphoma
- Recurrent Grade 1 Follicular Lymphoma
- Recurrent Grade 2 Follicular Lymphoma
- Recurrent Marginal Zone Lymphoma
- Recurrent Small Lymphocytic Lymphoma
- Splenic Marginal Zone Lymphoma
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Ipilimumab — BIOLOGICALA dose of 10 mg in cohort 1 or 25mg in cohort 2 via intratumoral injection on day 2, week 1.
- SD-101 — DRUGStarted on day 2 week 1, then once every week x 4 successive weeks for a total of 5 injections.
- Radiation therapy — RADIATIONUndergo low-dose radiation therapy to 1 site of disease
Study Details
This phase 1-2 trial studies the side effects and best dose of ipilimumab in combination with toll-like receptor 9 (TLR9) agonist SD-101 and radiation therapy in treating patients with recurrent low-grade B-cell lymphoma.
Key Dates
- Start date
- Sep 30, 2014
- Status verified
- Feb 2017
- Primary completion
- Nov 10, 2016
- Completion
- Jan 26, 2017
Study Design
- Enrollment
- 9 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: TreatmentPatients receive TLR9 agonist SD-101 via intratumoral injections; ipilimumab via intratumoral injection; and undergo radiation therapy on days 1 and 2.
Primary Outcome Measure
Number of Dose-limiting Toxicity (DLT) Events of Ipilimumab Plus a Fixed Dose of SD-101 (1 mg/Week) [ Time Frame: Up to 10 weeks ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Stanford University Hospitals and Clinics | Stanford | California | 94305 | - |
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