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NCT00061620

Phase I Study of Continuous Infusion Schedule of FMdC in Hematologic Malignancies

Completed Phase 1 Last updated 1 November 2018
What this trial tests

Phase 1 trial testing Tezacitabine (FMdC) in Hematologic Malignancies in 19 participants. Completed in 12 February 2004.

Timeline
6 September 2001
Primary endpoint
12 February 2004
12 February 2004

Quick facts

Lead sponsorM.D. Anderson Cancer Center
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationnon randomized
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment19
Start date6 September 2001
Primary completion12 February 2004
Estimated completion12 February 2004
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

M.D. Anderson Cancer Center — full company profile →

Who can join

15 and older, any sex, with Hematologic Malignancies. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The goal of this clinical research study is to find the highest dose of Tezacitabine (FMdC) which can be safely given as a continuous infusion by vein to patients with hematologic malignancies. The general safety and effectiveness of this drug will also be studied.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Hematologic Malignancies

Currently open trials in the same condition.

Other M.D. Anderson Cancer Center 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/NCT00061620.

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