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NCT03319914: OF-CALISTA

Observational Follow-up to ST-001 Calciphylaxis Pain Treatment With Intravenous Sodium Thiosulfate

Terminated Last updated 20 November 2018
What this trial tests

trial in Calciphylaxis in 5 participants. Terminated before completion.

Timeline
20 October 2017
Primary endpoint
9 November 2018
9 November 2018

Quick facts

Lead sponsorHope Pharmaceuticals
StatusTerminated
Study typeOBSERVATIONAL
Enrollment5
Start date20 October 2017
Primary completion9 November 2018
Estimated completion9 November 2018
Sites3 locations across United States

Conditions studied

Sponsor

Hope Pharmaceuticals

Who can join

18 and older, any sex, with Calciphylaxis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is an 8-week observational follow-up study of patients who participated in the ST-001 CALISTA study (A Phase 3, Intravenous Sodium Thiosulfate for Acute Calciphylaxis Treatment: A Multicenter, Randomized, Double-blind, Placebo-controlled Clinical Trial).

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Management of Cutaneous Calciphylaxis.
    Kodumudi V, Jeha GM, Mydlo N, Kaye AD. · · 2020 · cited 23× · PMID 32997277 · DOI 10.1007/s12325-020-01504-w

Verify or expand the search:

Other recruiting trials for Calciphylaxis

Currently open trials in the same condition.

Other Hope Pharmaceuticals trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03319914.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing