CompletedPhase 1NCT02728492
Safety, Tolerability and Pharmacokinetics of Quisinostat, a Histone Deacetylase Inhibitor, in Combination With Chemotherapy
Studying Malignant non-epithelial tumor of ovary
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- NewVac LLC
- Principal Investigator
- Sergey Tjulandin, ProfRussian Oncological Research Center n.a. N. N. Blokhin RAMS
- Intervention
- Quisinostat(drug)
- Enrollment
- 51 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2013 – 2016
Study locations (6)
- Russian Oncological Research Center n.a. N. N. Blokhin RAMS, Moscow, Russia
- State Budgetary Healthcare Institution of Stavropol Territory "Pyatigorsk oncology dispensary", Pyatigorsk, Russia
- Saint-Peterburg State Budgetary healthcare Institution "City Clinical Oncology Dispensary", Saint Petersburg, Russia
- BioEq LLC, Saint Petersburg, Russia
- State Budget Institution of healthcare "Saint-Petersburg clinical research and practical centre of specialized medical aid (oncology)", Saint Petersburg, Russia
- State Healthcare Institution of Yaroslavl region "Regional Clinical oncology hospital", Yaroslavl, Russia
Collaborators
Janssen Pharmaceutica N.V., Belgium
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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