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Trial · NCT01622660

Gemcitabine and Pazopanib in Chemotherapy Naïve Patients With Advanced/Metastatic Urothelial Carcinoma Ineligible for Cisplatin-based Chemotherapy

NCT01622660, Phase 2, Terminated, Memorial Sloan Kettering Cancer Center; results first posted 2017-08-22

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Gemcitabine and Pazopanib in Chemotherapy Naïve Patients With Advanced/Metastatic Urothelial Carcinoma Ineligible for Cisplatin-based Chemotherapy. Trials, record NCT01622660. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT01622660

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Trial

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

Title
Gemcitabine and Pazopanib in Chemotherapy Naïve Patients With Advanced/Metastatic Urothelial Carcinoma Ineligible for Cisplatin-based Chemotherapy
NCT number
NCT01622660
Status
Terminated
Phases
Phase 2
Enrollment
2 participants, actual
Lead sponsor
Memorial Sloan Kettering Cancer Center
Conditions
Bladder Cancer
Interventions
Gemcitabine, Pazopanib
First posted
2012-06-19
Last updated
2017-08-22
Results first posted
2017-08-22

Source ClinicalTrials.gov

Registered outcomes1

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

ListOutcomeTime frameDescription
PrimaryProgression Free Survival (PFS)2 years
Progression Free Survival will be calculated from the start of treatment until progressive disease or death. Patients who die before documented progression will be considered failures at their time of death. If the patient did not progress or die, the patient will be censored on the date of last follow-up. Response and progression will be evaluated in this study using the international criteria by the Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1 Measurable lesions: lesions that can be accurately measured in at least one dimension with longest diameter ≥ 10 mm by clinical exam or with spiral CT scan or MRI (no less than double the slice thickness and a minimum of 10mm). Malignant lymph nodes must be 15 mm in the short axis when assessed by spiral CT scan to be considered measurable. Non-measurable lesions: all other lesions (or sites of disease) including small lesions (longest diameter \< 20 mm with conventional techniques or \< 10 mm u

Outcomes1

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYProgression Free Survival (PFS)2 yearsdaysNUMBER

Results by group1

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

OutcomeGroupCategoryValueSpreadUnits
Progression Free Survival (PFS)Gemcitabine and Pazopanib184days

Participant flow3

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDGemcitabine and Pazopanib2
Overall StudyCOMPLETEDGemcitabine and Pazopanib1
Overall StudyNOT COMPLETEDGemcitabine and Pazopanib1

Adverse events28

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

TypeEventOrgan systemGroupAffectedAt riskEvents
otherElevated ALTHepatobiliary disordersGemcitabine and Pazopanib12
otherLymphopeniaBlood and lymphatic system disordersGemcitabine and Pazopanib12
otherElevated Alkaline PhosphataseHepatobiliary disordersGemcitabine and Pazopanib12
otherAnemiaBlood and lymphatic system disordersGemcitabine and Pazopanib12
otherElevated ASTHepatobiliary disordersGemcitabine and Pazopanib12
otherBlood Bilrubin IncreasedHepatobiliary disordersGemcitabine and Pazopanib12
otherConstipationGastrointestinal disordersGemcitabine and Pazopanib12
otherDiarrheaGastrointestinal disordersGemcitabine and Pazopanib12
otherDysgeusiaNervous system disordersGemcitabine and Pazopanib12
otherFatigueGeneral disordersGemcitabine and Pazopanib22

Adverse event totals3

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityGemcitabine and Pazopanib02
Total, other adverse eventsGemcitabine and Pazopanib22
Total, serious adverse eventsGemcitabine and Pazopanib12

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/NCT01622660

GET https://conductscience.org/api/trials/v1/NCT01622660/events?page=2