All terms in NCIT
| Label | Id | Description |
|---|---|---|
| Analgesic Agent | NCIT_C241 | [Compounds that alleviate pain without loss of consciousness. Analgesics act by various mechanisms including binding with opioid receptors and decreasing inflammation. Choice of analgesic may be determined by the type of pain. These compounds include opioid, non-opioid and adjuvant analgesic agents.] |
| Neoantigen-based Melanoma-Poly-ICLC Vaccine | NCIT_C112003 | [A peptide-based melanoma cancer vaccine consisting of neoantigens and peptides derived from patient-specific melanoma immunogenic epitopes, combined with the immunostimulant poly-ICLC with potential immunomodulating and antineoplastic activities. Vaccination with the neoantigen-based melanoma vaccine stimulates the host immune system to mount a cytotoxic T lymphocyte (CTL) response against tumor cells expressing the neoantigens, which results in tumor cell lysis. The adjuvant poly-ICLC, composed of double-stranded RNA molecules of polyinosinic-polycytidylic acid stabilized with poly L-lysine in carboxymethylcellulose, is a ligand for toll-like receptor-3 (TLR3) and induces the release of cytokines which may help to boost the immune response against the selected neoantigens.] |
| Melanoma Vaccine | NCIT_C2517 | |
| p70S6K/Akt Inhibitor MSC2363318A | NCIT_C112004 | [An orally available inhibitor of the serine/threonine protein kinases ribosomal protein S6 Kinase (p70S6K) and Akt (protein kinase B), with potential antineoplastic activity. Upon administration, p70S6K/Akt inhibitor MSC2363318A binds to and inhibits the activity of p70S6K and Akt. This prevents the activation of the PI3K/Akt/p70S6K signaling pathway and inhibits tumor cell proliferation in cancer cells that have an overactivated PI3K/Akt/p70S6K signaling pathway. Constitutive activation and dysregulated signaling of the PI3K/Akt/p70S6K pathway are frequently associated with tumorigenesis of many tumor types; targeting multiple kinases in this pathway is more efficacious than targeting a single kinase.] |
| Adenovirus 5-Human Guanylyl Cyclase C-PADRE Vaccine | NCIT_C112005 | [A replication-defective, recombinant adenoviral serotype 5 (Ad5) encoding human guanylyl cyclase C (hGCC) and the synthetic Pan DR epitope (PADRE), with potential antineoplastic and immunomodulating activities. Upon intramuscular administration, the Ad5-hGCC-PADRE vaccine expresses hGCC, which may induce both humoral and cellular immune responses against tumor cells expressing the hGCC antigen. This results in the immune-mediated inhibition of tumor cell proliferation, and leads to tumor death. The hGCC protein is normally restricted to intestinal epithelial cells but is overexpressed by metastatic colorectal tumors. PADRE is a helper T-lymphocyte epitope that is able to augment the magnitude and duration of the cytotoxic T-lymphocyte (CTL) response.] |
| Control Type | NCIT_C49647 | [A characteristic of a treatment regimen employed as a comparator against which the study treatment is evaluated.] |
| Placebo Control | NCIT_C49648 | [Use of an inactive compound identical in appearance to drug or treatment being tested in experimental research, which may or may not be known to the physician and/or subject, administered to distinguish between drug action and suggestive effect of the drug or treatment under study. The effects of the active drug or treatment are compared to the effects of the placebo.] |
| Active Control | NCIT_C49649 | [The use of a pharmacologic substance as a control within a treatment regimen where the pharmacologic properties of that substance are relevant to the condition being treated.] |
| Oraxol | NCIT_C112000 | [A combination formulation composed of a capsule containing the taxane compound paclitaxel and a tablet containing the multidrug resistance (MDR) efflux pump P-glycoprotein (P-gp) inhibitor HM30181A, with potential antineoplastic activity. Upon oral administration of oraxol, the HM30181A moiety binds to and inhibits P-gp, which prevents P-gp-mediated efflux of paclitaxel, therefore enhancing its oral bioavailability. In turn, paclitaxel binds to and stabilizes microtubules, preventing their depolymerization, which results in the inhibition of cellular motility, mitosis, and replication. Altogether, this may result in greater intracellular concentration of paclitaxel, and enhanced cytotoxicity against tumor cells, when compared to the administration of paclitaxel alone. P-gp, encoded by the MDR-1 gene, is a member of the ATP-binding cassette (ABC) superfamily of transmembrane transporters; it prevents the intestinal uptake and intracellular accumulation of various cytotoxic agents.] |
| Anti-LIV-1 Monoclonal Antibody-MMAE Conjugate SGN-LIV1A | NCIT_C112001 | [An antibody-drug conjugate (ADC) composed of a humanized monoclonal antibody directed against the anti-solute carrier family 39 zinc transporter member 6 (SLC39A6; LIV-1; ZIP6) protein that is conjugated, via a protease-cleavable linker, to the cytotoxic agent monomethyl auristatin E (MMAE), with potential antineoplastic activity. Upon administration and internalization by LIV-1-positive tumor cells, anti-LIV-1 antibody-drug conjugate SGN-LIV1A undergoes enzymatic cleavage to release MMAE into the cytosol. In turn, MMAE binds to and inhibits tubulin polymerization, which may result in G2/M phase cell cycle arrest and apoptosis in LIV-1-expressing tumor cells. LIV-1, a member of the zinc transporter family, is expressed in several types of solid tumors and plays a key role in tumor cell progression and metastasis. The linkage system in SGN-LIV1A is highly stable in plasma, resulting in cytotoxic specificity against LIV-1-positive cells.] |
| Cure Study | NCIT_C49654 | [A type of study protocol designed to evaluate intervention(s) aimed to cure a disease or condition.] |
| Clinical Study by Intent | NCIT_C49652 | [The name of a code list that contains terms to define the type of trial, e.g. cure or prevention.] |
| Anti-Carcinoembryonic Antigen Antibody-Carboxypeptidase G2 Fusion Protein MFECP1 | NCIT_C74600 | |
| Adverse Effect Mitigation Study | NCIT_C49655 | [A type of study designed to identify actions necessary to eliminate or reduce the risk to human life or well-being as a result of a particular medication, treatment regimen, procedure, or any other medical intervention.] |
| Parenchyma | NCIT_C74601 | [The tissue that constitutes the essential part of an organ as contrasted with e.g., connective tissue and blood vessels.] |
| Treatment Study | NCIT_C49656 | [A type of study protocol designed to evaluate intervention(s) for disease treatment.] |
| Mitotic Figure | NCIT_C74602 | [The microscopic appearance of a cell undergoing mitosis.] |
| Prevention Study | NCIT_C49657 | [A type of study protocol designed to evaluate intervention(s) for disease prevention.] |
| Diagnosis Group | NCIT_C49650 | [A grouping of individuals on the basis of a shared procedure or disease, or lack thereof (e.g. healthy volunteers, type 2 diabetic subjects, subjects with renal cell cancer). Standardized naming systems are available that define the groups within which a subject should be placed.] |
| Group | NCIT_C43359 | [Any number of entities (members) considered as a unit.] |