Drugs / PROSTVAC-F

Trials 14 · a red edge is where a trial was stopped

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 12 trials
Phase 1 NCT03532217 Sep 2018 → Apr 2022 metastatic prostate carcinoma Washington University School of Medicine Completed No outcome recorded
Phase 1 NCT00113984 Jun 2005 → Feb 2008 prostate neoplasm National Cancer Institute (NCI) Completed No outcome recorded
Phase 1/22 trials
Phase 1/2 NCT02933255 Apr 2017 → Jun 2023 prostate cancer National Cancer Institute (NCI) Completed No outcome recorded
Phase 1/2 NCT00060528 May 2003 → Mar 2006 prostate neoplasm National Cancer Institute (NCI) Completed No outcome recorded
Phase 29 trials
Phase 2 NCT03315871 Mar 2018 → Jun 2024 prostate cancer National Cancer Institute (NCI) Completed No outcome recorded
Phase 2 NCT02772562 Jul 2016 → Apr 2024 prostate cancer Medical University of South Carolina Terminated No outcome recorded
Phase 2 NCT02649855 Jan 2016 → Jul 2022 prostate cancer National Cancer Institute (NCI) Completed No outcome recorded
Phase 2 NCT02649439 Dec 2015 → Mar 2019 prostate cancer National Cancer Institute (NCI) Completed No outcome recorded
Phase 2 NCT02153918 May 2014 → Jul 2017 prostate cancer National Cancer Institute (NCI) Completed No outcome recorded
Phase 2 NCT01875250 Jul 2013 → Sep 2019 prostate cancer National Cancer Institute (NCI) Completed No outcome recorded
Phase 2 NCT00450463 Feb 2007 → Apr 2017 prostate cancer National Cancer Institute (NCI) Completed No outcome recorded
Phase 2 NCT00450619 Feb 2007 → Nov 2012 prostate cancer National Cancer Institute (NCI) Completed No outcome recorded
Phase 2 NCT00108732 Feb 2006 → Oct 2010 grade III prostatic intraepithelial neoplasia National Cancer Institute (NCI) Completed No outcome recorded
Phase 31 trial
Phase 3 NCT01322490 Nov 2011 → Sep 2017 metastatic prostate carcinoma Bavarian Nordic Completed No outcome recorded

Evidence & citations 7 cited values

Every value below carries the sentence it was read from. 15 sources stand behind the page.

FieldValueCited text
Known as PROSTVAC-F PROSTVAC-F (fowlpox) will be administered subcutaneously in an extremity (e.g., thigh) at a dose of 1x10\^9 infectious units.” NCT02933255
8

“0.5 ml containing at least 1 x 109 Inf.U PROSTVAC-F given on days 15, 28, 57, 85, 113, 141.” NCT02772562

PROSTVAC-F (Fowlpox)/TRICOM” NCT00108732

NCT01322490

NCT02649439

NCT03315871

NCT03532217

NCT01875250

NCT02649855

Known as PROSTVAC-F (rilimogene galvacirepvec/rilimogene glafolivec)/TRICOM (triad of costimulatory molecules PROSTVAC-F (rilimogene galvacirepvec/rilimogene glafolivec)/TRICOM (triad of costimulatory moleculesNCT00450463
Known as PROSTVAC-F/TRICOM PROSTVAC-F/TRICOM (fowlpox) 1 x 10\^9 pfu subcutaneously on days 15, 29, and then every 4 weeks.” NCT00450619
4

NCT00060528

NCT00450463

NCT02153918

NCT00113984

Known as Recombinant Fowlpox-PSA (L155)-TRICOM “Drug: Recombinant Fowlpox-PSA (L155)-TRICOM (PROSTVAC-F/TRICOM)” NCT00060528
Action Deplete “The immune stimulating vaccine will help white blood cells recognize and kill the cancer cells throughout the body.” NCT01875250
Modality Vaccine “a vaccine using recombinant vaccinia virus (prime) and recombinant fowlpox virus (boost)” PMID 17707059 Aug 2007
Route Subcutaneous “Given SC” NCT00108732