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Trial · NCT00858572

STA-9090 for Treatment of AML, CML, MDS and Myeloproliferative Disorders

NCT00858572, Phase 1, Completed, Synta Pharmaceuticals Corp.

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. STA-9090 for Treatment of AML, CML, MDS and Myeloproliferative Disorders. Trials, record NCT00858572. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00858572

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
STA-9090 for Treatment of AML, CML, MDS and Myeloproliferative Disorders
NCT number
NCT00858572
Status
Completed
Phases
Phase 1
Enrollment
31 participants, actual
Lead sponsor
Synta Pharmaceuticals Corp.
Conditions
AML, CML, MDS, Myeloproliferative Disorders
Interventions
STA-9090 (ganetespib)
First posted
2009-03-10
Last updated
2014-09-18

Source ClinicalTrials.gov

Registered outcomes6

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryTo characterize the safety and tolerability of STA-9090 (ganetespib) in subjects with hematologic malignanciesFeb 2011
PrimaryTo assess preliminary evidence of anti-neoplastic activityFeb 2011
PrimaryTo assess the pharmacokinetics of STA-9090 (ganetespib) when administered as a short-term intravenous infusionFeb 2011
SecondaryTo assess changes in biomarkers following study drug administrationFeb 2011
SecondaryTo investigate drug exposure levels/plasma concentrations and correlations with efficacy and safety parametersFeb 2011
SecondaryTo assess the impact of variations in drug metabolizing enzymes (DME pharmacogenomics) on the pharmacokinetics of STA-9090 (ganetespib)Feb 2011

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT00858572

GET https://conductscience.org/api/trials/v1/NCT00858572/registered