Trial · NCT00568750
Dasatinib as First-Line Therapy in Treating Patients With Gastrointestinal Stromal Tumors
NCT00568750, Phase 2, Completed, Swiss Cancer Institute
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Dasatinib as First-Line Therapy in Treating Patients With Gastrointestinal Stromal Tumors. Trials, record NCT00568750. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00568750
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Dasatinib as First-Line Therapy in Treating Patients With Gastrointestinal Stromal Tumors
- NCT number
- NCT00568750
- Status
- Completed
- Phases
- Phase 2
- Enrollment
- 47 participants, actual
- Lead sponsor
- Swiss Cancer Institute
- Conditions
- Gastrointestinal Stromal Tumor
- Interventions
- dasatinib
- First posted
- 2007-12-06
- Last updated
- 2019-06-17
- Other registries' IDs
- eudract:2007-002047-24
Source ClinicalTrials.gov
Registered outcomes9
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Response as assessed by fusion PET/CT scan according to EORTC PET Study Group criteria | at 4 weeks compared to baseline | |
| Secondary | Best response as assessed by CT scan/MRI | according to RECIST criteria | |
| Secondary | Best response as assessed by fusion PET/CT scan | at 4 weeks | |
| Secondary | Clinical benefit | Clinical benefit is defined as CR, PR, or as SD lasting at least 12 weeks, determined according to RECIST | |
| Secondary | Time to progression | calculated from registration until progression or death due to tumor | |
| Secondary | Progression-free survival | calculated from registration until progression or death | |
| Secondary | Time to treatment failure | calculated from registration until premature trial treatment termination due to any reason | |
| Secondary | Overall survival | Overall survival will be calculated from registration until death or last follow-up, up to 5 years. | |
| Secondary | Adverse drug reactions according to NCI CTCAE v3.0 | Tolerability will be assessed based on the frequency and severity of Adverse Drug Reactions (ADR) coded according to NCI CTCAE v3.0. |
Source ClinicalTrials.gov
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.
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/NCT00568750
GET https://conductscience.org/api/trials/v1/NCT00568750/registered