Drugs / recombinant vaccinia-CEA(6D)-TRICOM vaccine
last change Mar 2015 re-read 9 days ago

recombinant vaccinia-CEA(6D)-TRICOM vaccine

Vaccine

Developed for
female breast carcinoma · lung cancer
Investigated by
National Cancer Institute (NCI)

Trials 2

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PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 21 trial
Phase 2 NCT00052351 Sep 2002 → Oct 2007 female breast carcinoma National Cancer Institute (NCI) Completed No outcome recorded
Phase not applicable1 trial
— NCT00091039 Aug 2004 → Feb 2006 lung cancer National Cancer Institute (NCI) Completed No outcome recorded
Comparator or background therapy2 trials
Phase 1 NCT00217373 Background Jun 2005 → Jan 2013 neoplasm National Cancer Institute (NCI) Completed No outcome recorded
Phase 1 NCT00088933 Background Jun 2004 → Nov 2007 non-small cell lung carcinoma, rectal carcinoma, small cell lung carcinoma National Cancer Institute (NCI) Terminated No outcome recorded

Evidence & citations 5 cited values

Every value below carries the sentence it was read from. 4 sources stand behind the page.

FieldValueCited text
Known as recombinant vaccinia-CEA(6D)-TRICOM vaccine ClinicalTrials.gov intervention name — accepted as the source's own label NCT00052351 ↗
3

NCT00217373 ↗

NCT00088933 ↗

NCT00091039 ↗

Known as vaccinia-CEA-TRICOM vaccine “Patients receive vaccinia-CEA-TRICOM vaccine subcutaneously (SC) on day 0 and fowlpox-CEA-TRICOM (rF-CEA-TRICOM) vaccine SC on days 14, 29, 43, 57, 70, 91, and 112.” NCT00091039 ↗
Action Deplete “Vaccines may make the body build an immune response to kill tumor cells.” NCT00088933 ↗
Modality Vaccine “Vaccines made from a gene-modified virus may make the body build an immune response to kill tumor cells.” NCT00052351 ↗
Route Subcutaneous “all patients receive vaccinia-CEA-TRICOM vaccine subcutaneously (SC) on day 1” NCT00052351 ↗