Drugs / Dociparstat

Trials 6 · a red edge is where a trial was stopped

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 12 trials
Phase 1 NCT02995655 Apr 2017 → Sep 2018 acute myeloid leukemia, myelodysplastic syndrome Washington University School of Medicine Completed No outcome recorded
Phase 1 NCT02056782 Dec 2013 → Feb 2015 acute myeloid leukemia Jazz Pharmaceuticals Completed No outcome recorded
Phase 22 trials
Phase 2 NCT02873338 Aug 2016 → Jun 2019 acute myeloid leukemia Jazz Pharmaceuticals Completed No outcome recorded
Phase 2 NCT01461915 Nov 2011 → Dec 2012 malignant pancreatic neoplasm Jazz Pharmaceuticals Terminated No outcome recorded
Phase 2/31 trial
Phase 2/3 NCT04389840 Jul 2020 → May 2021 COVID-19, acute lung injury Jazz Pharmaceuticals Terminated No outcome recorded
Phase 31 trial
Phase 3 NCT04571645 Apr 2021 → May 2022 acute myeloid leukemia Jazz Pharmaceuticals Terminated No outcome recorded

Evidence & citations 6 cited values

Every value below carries the sentence it was read from. 6 sources stand behind the page.

FieldValueCited text
Known as Dociparstat ClinicalTrials.gov intervention name — accepted as the source's own label NCT01461915
3

NCT04389840

NCT04571645

NCT02056782

Known as CX-01 ClinicalTrials.gov intervention name — accepted as the source's own label NCT02995655
Known as dociparstat sodium “This was a randomized, double-blind, placebo-controlled Phase 2/3 study to evaluate the safety and efficacy of dociparstat sodium in adult patients with acute lung injury (ALI)...” NCT04389840
2

“A Pilot Study of Dociparstat Sodium (ODSH) in Acute Myeloid Leukemia” NCT02056782

NCT02873338

Action Inhibit “Autophagy appears to be largely driven by the binding of high mobility group box-1 protein (HMGB1) to the receptor for advanced glycation end-products (RAGE), which is strongly...” NCT01461915
Modality Other / unclassified “Dociparstat is a glycosaminoglycan derived from porcine heparin.” NCT04389840
Route Intravenous “dociparstat IV bolus at 4 mg/kg will be administered in 5 minutes immediately after completion of gemcitabine administration.” NCT01461915