Trials / Terminated
TerminatedNCT03586869
QUILT-3.080: NANT Pancreatic Cancer Vaccine
QUILT-3.080: Phase 1B/2 Trial Of The NANT Pancreatic Cancer Vaccine As Treatment For Subjects With Pancreatic Cancer Who Have Progressed on or After Standard-Of-Care Therapy
- Status
- Terminated
- Phase
- Phase 1 / Phase 2
- Study type
- Interventional
- Enrollment
- 3 (actual)
- Sponsor
- ImmunityBio, Inc. · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This is a phase 1b/2 study to evaluate the safety and efficacy of metronomic combination therapy in subjects with pancreatic cancer who have progressed on or after previous Standard of Care (SoC) chemotherapy.
Detailed description
Treatment will be administered in two phases, an induction and a maintenance phase, as described below. Subjects will continue induction treatment for up to 1 year. Treatment in the study will be discontinued if the subject experiences progressive disease (PD) or unacceptable toxicity (not corrected with dose reduction), withdraws consent, or if the Investigator feels it is no longer in the subject's best interest to continue treatment. Those who have a complete response (CR) in the induction phase will enter the maintenance phase of the study. Subjects who experience ongoing stable disease (SD) or an ongoing partial response (PR) at 1 year may enter the maintenance phase at the Investigator's discretion. Subjects may remain on the maintenance phase of the study for up to 1 year. Treatment will continue in the maintenance phase until the subject experiences PD or unacceptable toxicity (not corrected with dose reduction), withdraws consent, or if the Investigator feels it is no longer in the subject's best interest to continue treatment. The maximum time on study treatment, including both the induction and maintenance phases, is 2 years.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Aldoxorubicin HCl | Aldoxorubicin Hydrochloride |
| BIOLOGICAL | ALT-803 | Recombinant human super agonist interleukin-15 (IL-15) complex |
| BIOLOGICAL | ETBX-011 | Ad5 \[E1-, E2b-\]-CEA |
| BIOLOGICAL | ETBX-021 | Ad5 \[E1-, E2b-\]-HER2 |
| BIOLOGICAL | ETBX-051 | Ad5 \[E1-, E2b-\]-Brachyury |
| BIOLOGICAL | ETBX-061 | Ad5 \[E1-, E2b-\]-MUC1 |
| BIOLOGICAL | GI-4000 | RAS yeast |
| BIOLOGICAL | GI-6207 | Carcinoembryonic Antigen (CEA) yeast |
| BIOLOGICAL | GI-6301 | Brachyury yeast |
| BIOLOGICAL | haNK for infusion | NK-92 \[CD16.158V, ER IL-2\] |
| BIOLOGICAL | bevacizumab | Recombinant human anti-Vascular Endothelial Growth Factor (VEGF) IgG1 monoclonal |
| DRUG | Capecitabine | 5'-deoxy-5-fluoro-N-\[(pentyloxy) carbonyl\]-cytidine |
| DRUG | Cyclophosphamide | 2-\[bis(2-chloroethyl)amino\]tetrahydro-2H-1,3,2-oxazaphosphorine 2-oxide monohydrate |
| DRUG | Fluorouracil | 5-fluoro-2,4 (1H,3H)-pyrimidinedione |
| DRUG | Leucovorin | L-Glutamic acid, N-\[4-\[\[(2-amino-5-formyl-1,4,5,6,7,8-hexahydro-4-oxo-6-pteridinyl)methyl\]amino\]benzoyl\]-, calcium salt |
| DRUG | nab-Paclitaxel | Benzenepropanoic acid, β-(benzoylamino)-α-hydroxy-(2aR, 4S, 4aS, 6R, 9S, 11S, 12S, 12aR, 12bS)-6,12b-bis(acetyloxy)-12-(benzoyloxy)-2a, 3, 4, 4a, 5, 6, 9, 10, 11, 12, 12a, 12b-dodecahydro-4,11-dihydroxy-4a, 8, 13, 13-tetramethyl-5-oxo-7,11-methano-1H-cyclodeca\[3,4\]benz\[1,2-b\]oxet-9-y1ester,(αR,βS)-(9CI) bound to albumin |
| DRUG | Oxaliplatin | cis-\[(1 R,2 R)-1,2-cyclohexanediamine-N,N'\] \[oxalato(2-)- O,O'\] platinum |
| BIOLOGICAL | Avelumab | Recombinant human anti-programmed death-ligand 1 (PD-L1) IgG1 monoclonal antibody |
| PROCEDURE | SBRT | Stereotactic Body Radiation Therapy |
Timeline
- Start date
- 2018-07-17
- Primary completion
- 2019-04-17
- Completion
- 2019-08-01
- First posted
- 2018-07-16
- Last updated
- 2024-08-27
- Results posted
- 2024-08-27
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT03586869. Inclusion in this directory is not an endorsement.