Drugs / pyrazoloacridine
pyrazoloacridine
Trials 8
Evidence & citations 7 cited values
Every value below carries the sentence it was read from. 10 sources stand behind the page.
| Field | Value | Cited text |
|---|---|---|
| Known as | pyrazoloacridine | ClinicalTrials.gov intervention name — accepted as the source's own label NCT00053950 ↗ |
| Known as | NSC-366140 | “A Phase II Trial of Pyrazoloacridine (NSC 366140, IND 36325) in Metastatic Cutaneous and Ocular Melanoma” NCT00003802 ↗1“Pyrazoloacridine, PZA, NSC-366140.” NCT00002656 ↗ |
| Known as | NSC-627168 | ChEMBL registry synonym — accepted as the source's own label CHEMBL118841 ↗ |
| Known as | PD 115934 | ChEMBL registry synonym — accepted as the source's own label CHEMBL118841 ↗ |
| Known as | PZA | “Pyrazoloacridine (PZA), a rationally synthesized acridine derivative, has shown promising antitumor activity against glioma lines in combination with platinum compounds.” PMID 16133802 ↗ Oct 20054“All patients receive intravenous pyrazoloacridine (PZA) every 3 weeks in the absence of progressive disease or unacceptable toxicity.” NCT00002585 ↗ “Patients receive pyrazoloacridine (PZA) IV over 3 hours on day 1.” NCT00006355 ↗ “Pyrazoloacridine, PZA, NSC-366140.” NCT00002656 ↗ “PZA” NCT00003714 ↗ |
| Modality | Small molecule | “Pyrazoloacridine (PZA), a rationally synthesized acridine derivative” PMID 16133802 ↗ Oct 2005 |
| Route | Intravenous | “All patients receive intravenous pyrazoloacridine (PZA) every 3 weeks in the absence of progressive disease or unacceptable toxicity.” NCT00002585 ↗ |