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Trial · NCT02560012

Personalized Targeted Inhibitors Treatment in Renal Cell Cancer

NCT02560012, Phase 2, Terminated, The University of Texas Health Science Center, Houston; results first posted 2018-10-12

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Personalized Targeted Inhibitors Treatment in Renal Cell Cancer. Trials, record NCT02560012. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT02560012

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Trial

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

Title
Personalized Targeted Inhibitors Treatment in Renal Cell Cancer
NCT number
NCT02560012
Status
Terminated
Phases
Phase 2
Enrollment
4 participants, actual
Lead sponsor
The University of Texas Health Science Center, Houston
Conditions
Carcinoma, Renal Cell
Interventions
Sunitinib, Temsirolimus, Sorafenib, Pazopanib, Everolimus, Axitinib
First posted
2015-09-25
Last updated
2018-10-12
Results first posted
2018-10-12

Source ClinicalTrials.gov

Registered outcomes1

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

ListOutcomeTime frameDescription
PrimaryNumber of Participants Who ProgressedFrom date of enrollment until the date of first documented progression, date of death from any cause, or date that the study was stopped, whichever came first, an average of 16 months
The PFS is defined as the time elapsed between treatment initiation and tumor progression or death from any cause, with censoring of patients who are lost to follow-up. Progression is defined using the Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.1): " At least a 20% increase in the sum of diameters of target lesions, taking as reference the smallest sum on study (this includes the baseline sum if that is the smallest on study). In addition to the relative increase of 20, the sum must also demonstrate an absolute increase of at least 5 mm. (Note: the appearance of one or more new lesions is also considered progression)."

Outcomes1

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYNumber of Participants Who ProgressedFrom date of enrollment until the date of first documented progression, date of death from any cause, or date that the study was stopped, whichever came first, an average of 16 monthsAll participants who received personalized therapy (sunitinib, temsirolimus, sorafenib, or pazopanib) based on their tumor's profile.ParticipantsCOUNT_OF_PARTICIPANTS

Results by group1

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

OutcomeGroupCategoryValueSpreadUnits
Number of Participants Who ProgressedPersonalized Therapy0Participants

Participant flow3

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDPersonalized Therapy3
Overall StudyCOMPLETEDPersonalized Therapy1
Overall StudyNOT COMPLETEDPersonalized Therapy2

Adverse events42

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

TypeEventOrgan systemGroupAffectedAt riskEvents
otherAbdominal painGastrointestinal disordersPersonalized Therapy131
otherAnaphylaxisImmune system disordersPersonalized Therapy131
otherAnemiaBlood and lymphatic system disordersPersonalized Therapy131
otherBack painMusculoskeletal and connective tissue disordersPersonalized Therapy232
otherBloatingGastrointestinal disordersPersonalized Therapy132
otherBone painMusculoskeletal and connective tissue disordersPersonalized Therapy131
otherBronchial infectionInfections and infestationsPersonalized Therapy131
otherBullous dermatitisSkin and subcutaneous tissue disordersPersonalized Therapy131
otherConstipationGastrointestinal disordersPersonalized Therapy132
otherCoughRespiratory, thoracic and mediastinal disordersPersonalized Therapy131

Adverse event totals3

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityPersonalized Therapy03
Total, other adverse eventsPersonalized Therapy33
Total, serious adverse eventsPersonalized Therapy03

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/NCT02560012

GET https://conductscience.org/api/trials/v1/NCT02560012/events?page=2