Last reviewed · How we verify
NCT00195104
Arsenic Trioxide in Combination With Cytarabine in Patients With High-risk MDS and Poor-prognosis AML
Phase 1, PHASE2 trial testing Arsenic Trioxide (Tricenox) in Myelodysplastic Syndrome in 87 participants. Completed in 20 June 2006.
17 March 2006
Quick facts
| Lead sponsor | Weill Medical College of Cornell University |
|---|---|
| Phase | Phase 1, PHASE2 |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | na |
| Design | single group |
| Masking | none |
| Primary purpose | treatment |
| Enrollment | 87 |
| Start date | 17 September 2003 |
| Primary completion | 17 March 2006 |
| Estimated completion | 20 June 2006 |
| Sites | 1 location across United States |
Drugs / interventions tested
- Arsenic Trioxide (Tricenox) — full drug profile →
- Cytarabine — full drug profile →
Conditions studied
- Myelodysplastic Syndrome — all drugs for Myelodysplastic Syndrome →
Sponsor
Weill Medical College of Cornell University
Who can join
18 and older, any sex, with Myelodysplastic Syndrome. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The purpose of this study is to find out the effectiveness and side effects of arsenic trioxide in combination with low-dose ara-C.
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Redox control of leukemia: from molecular mechanisms to therapeutic opportunities.
Irwin ME, Rivera-Del Valle N, Chandra J. · · 2013 · cited 111× · PMID 22900756 · DOI 10.1089/ars.2011.4258
Verify or expand the search:
- PubMed search for NCT00195104
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other recruiting trials for Myelodysplastic Syndrome
Currently open trials in the same condition.
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- NCT07107126 — Safety and Proof-of-Concept Study of RPT1G in Adults With Acute Myeloid Leukemia and High-Risk Myelodysplastic Syndromes · Phase 1 · recruiting
- NCT06781099 — Feasibility Trial of Extracorporeal Iron Purification in Patients With Myelodysplastic Syndrome or Myelofibrosis · NA · recruiting
- NCT07285044 — The Cancer Connected Access and Remote Expertise Beyond Walls Program to Provide In-Home Cancer Treatment and Improve Tr · Phase 2 · recruiting
Other Weill Medical College of Cornell University trials
Trials by the same sponsor.
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- NCT06818734 — Implementation of a Clinical Decision Support Tool for Postpartum Depression · NA · not yet recruiting
- NCT07485725 — Center for Research and Education on Aging and Technology Enhancement - CREATE V - Project 3 · NA · not yet recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT00195104 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Weill Medical College of Cornell University
- Last refreshed: 3 March 2017
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/NCT00195104.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing