Study of Repeat Intranodal Injections of Ad-ISF35
NCT00942409 · Status: TERMINATED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 5
Last updated 2015-12-30
Summary
This is a Phase II, open label, fixed dose, repeat injection, single institution study. Eligible subjects will receive up to six doses of Ad-ISF35 injected directly into a selected lymph node under ultrasound guidance. The primary goal is to determine and monitor clinical and biological responses in patients treated with repeat intranodal injections of Ad-ISF35.
Conditions
- Non-Hodgkin's Lymphoma
- Follicular Lymphoma
- Diffuse Large Cell Lymphoma
- Mantle Cell Lymphoma
- Small Lymphocytic Lymphoma
- Chronic Lymphocytic Leukemia
Interventions
- BIOLOGICAL
-
ISF35
Subjects participating in this study will be treated with multiple doses of Ad-ISF35 given via intranodal injection using a fixed dose of 3.3 x 10\^10 ISF35 viral particles. Intranodal injections will be administered every 2-4 weeks up to six total injections.
Sponsors & Collaborators
-
Memgen, LLC
collaborator INDUSTRY -
Januario Castro, M.D.
lead OTHER
Principal Investigators
-
Januario Castro, M.D. · Associate Clinical Professor in the Blood and Bone Marrow Transplantation Division
-
Thomas J Kipps, M.D., Ph.D. · Professor of Medicine, Evelyn and Edwin Tasch Chair in Cancer Research in the UCSD School of Medicine
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2009-06-30
- Primary Completion
- 2009-07-31
- Completion
- 2014-07-31
Countries
- United States
Study Locations
More Related Trials
-
A Study of Atezolizumab in Combination With an Immunotherapy Agent Investigated With or Without Anti-Cd20 Therapy in Patients With Relapsed or Refractory Non-Hodgkin Lymphoma
NCT03369964 ·Status: WITHDRAWN ·Phase: PHASE1
-
Denileukine Diftitox for Relapsed ALCL
NCT00801918 ·Status: WITHDRAWN ·Phase: PHASE2
-
Vorinostat and Lenalidomide in Treating Patients With Relapsed or Refractory Hodgkin Lymphoma or Non-Hodgkin Lymphoma
NCT01116154 ·Status: TERMINATED ·Phase: PHASE1
-
Aflibercept and Standard Chemotherapy (R-CHOP) in First Line of Non Hodgkin B-cell Lymphoma
NCT00644124 ·Status: COMPLETED ·Phase: PHASE1
-
Relmacabtagene Autoleucel As Second-Line Therapy in Adult Patients with Aggressive B-cell NHL
NCT06093841 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE2
-
SB-715992 in Treating Patients With Metastatic or Unresectable Solid Tumors or Hodgkin's or Non-Hodgkin's Lymphoma
NCT00101244 ·Status: TERMINATED ·Phase: PHASE1
-
Study of ADCT-301 in Patients With Relapsed or Refractory Hodgkin and Non-Hodgkin Lymphoma
NCT02432235 ·Status: COMPLETED ·Phase: PHASE1
-
Autologous or Donor Stem Cell Transplantation in Treating Patients With Recurrent Non-Hodgkin's Lymphoma (BMT CTN 0202)
NCT00096460 ·Status: TERMINATED ·Phase: PHASE2/PHASE3
-
Vorinostat and Combination Chemotherapy Before Donor Stem Cell Transplantation for the Treatment of Relapsed Aggressive B-cell or T-cell Non-Hodgkin Lymphoma
NCT04220008 ·Status: WITHDRAWN ·Phase: PHASE2
-
Study to Evaluate Safety, Tolerability, and Pharmacokinetics of Idelalisib in Japanese Participants With Relapsed or Refractory Indolent B-Cell Non-Hodgkin Lymphomas (iNHL) or Chronic Lymphocytic Leukemia (CLL)
NCT02242045 ·Status: COMPLETED ·Phase: PHASE1
-
Autologous Stem Cell Transplant Followed by Donor Stem Cell Transplant in Treating Patients With Relapsed or Refractory Lymphoma
NCT00005803 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
A Study Evaluating GDC-0980 Administered Once Weekly in Patients With Refractory Solid Tumors or Non-Hodgkin's Lymphoma
NCT00854126 ·Status: COMPLETED ·Phase: PHASE1
-
A Study to Assess Safety and Efficacy of CHO-H01 as a Single Agent/Combined With Lenalidomide in Subjects With Refractory or Relapsed Non-Hodgkin's Lymphoma
NCT05950165 ·Status: RECRUITING ·Phase: PHASE1/PHASE2
-
p53/p16-Independent Epigenetic Therapy With Oral Decitabine/Tetrahydrouridine for Refractory/Relapsed Lymphoid Malignancies
NCT02846935 ·Status: COMPLETED ·Phase: EARLY_PHASE1
-
A Phase I Dose Escalation Study of the Safety and Pharmacokinetics of LAM-002A In Patients With Non-Hodgkin's Lymphoma
NCT02594384 ·Status: COMPLETED ·Phase: PHASE1
-
Tagraxofusp and Low-Intensity Chemotherapy for the Treatment of CD123 Positive Relapsed or Refractory Acute Lymphoblastic Leukemia or Lymphoblastic Lymphoma
NCT05032183 ·Status: TERMINATED ·Phase: PHASE1/PHASE2
-
A Safety Study of PF-08046045/SGN-35T in Adults With Advanced Cancers
NCT06120504 ·Status: TERMINATED ·Phase: PHASE1
-
MEN1309 I.v. Infusion in Pts With CD205-positive Metastatic Solid Tumors and Relapsed or Refractory NHL Ph I Study
NCT03403725 ·Status: TERMINATED ·Phase: PHASE1
-
Safety, Pharmacokinetics, and Clinical Activity of LP-284 in Adult Patients With Relapsed or Refractory Lymphomas and Solid Tumors
NCT06132503 ·Status: RECRUITING ·Phase: PHASE1
-
Dose Augmented Rituximab and ICE for Pts With Primary Refractory and Poor Risk Relapsed Aggressive B-Cell NHL
NCT00588094 ·Status: COMPLETED ·Phase: PHASE2
-
Dose De-escalation Study of the PI3k Alpha/Delta Inhibitor, Copanlisib Given in Combination With the Immunotherapeutic Agents, Nivolumab and Rituximab in Patients With Relapsed/Refractory Indolent Lymphoma
NCT04431635 ·Status: TERMINATED ·Phase: PHASE1
-
Lenalidomide and Obinutuzumab in Treating Patients With Relapsed Indolent Non-Hodgkin Lymphoma
NCT01995669 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Study Evaluating the Safety and Efficacy of KTE-C19 in Adult Participants With Refractory Aggressive Non-Hodgkin Lymphoma
NCT02348216 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Combination Chemotherapy, Rituximab, and Ixazomib Citrate in Treating Patients With Non-Hodgkin Lymphoma
NCT02481310 ·Status: UNKNOWN ·Phase: PHASE1/PHASE2
-
A Study of YY-20394 in Participants With Relapsed/Refractory Follicular Non-Hodgkin's Lymphoma
NCT04370405 ·Status: UNKNOWN ·Phase: PHASE2