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Trial · NCT03370718

Cabozantinib in Treating Patients With Locally Advanced or Metastatic Unresectable Adrenocortical Carcinoma

NCT03370718, Phase 2, Completed, M.D. Anderson Cancer Center; results first posted 2024-12-10

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Cabozantinib in Treating Patients With Locally Advanced or Metastatic Unresectable Adrenocortical Carcinoma. Trials, record NCT03370718. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT03370718

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Trial

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

Title
Cabozantinib in Treating Patients With Locally Advanced or Metastatic Unresectable Adrenocortical Carcinoma
NCT number
NCT03370718
Status
Completed
Phases
Phase 2
Enrollment
18 participants, actual
Lead sponsor
M.D. Anderson Cancer Center
Conditions
Metastatic Carcinoma in the Adrenal Cortex, Stage III Adrenal Cortex Carcinoma AJCC v8, Stage IV Adrenal Cortex Carcinoma AJCC v8, Unresectable Adrenal Cortex Carcinoma
Interventions
Cabozantinib, Pharmacogenomic Study, Pharmacokinetic Study
First posted
2017-12-12
Last updated
2024-12-10
Results first posted
2024-12-10

Source ClinicalTrials.gov

Registered outcomes1

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

ListOutcomeTime frameDescription
PrimaryProgression-free Survival (PFS) as Defined by Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 CriteriaAt 4 months
PFS rates will be monitored simultaneously using the Bayesian approach of Thall, Simon, Esty as extended by Thall and Sung. PFS is defined as no disease progression or death within the first 4 months of the proposed treatment.

Outcomes1

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYProgression-free Survival (PFS) as Defined by Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 CriteriaAt 4 monthsprecentage of participantsNUMBER

Results by group1

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

OutcomeGroupCategoryValueSpreadUnits
Progression-free Survival (PFS) as Defined by Response Evaluation Criteria in Solid Tumors (RECIST) 1.1 CriteriaCabozantinib72.295% Confidence Interval 46.5 to 90.3precentage of participants

Participant flow3

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDCabozantinib18
Overall StudyCOMPLETEDCabozantinib17
Overall StudyNOT COMPLETEDCabozantinib1

Adverse events127

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

TypeEventOrgan systemGroupAffectedAt riskEvents
otherAbdominal painGastrointestinal disordersCabozantinib718
otherAcneSkin and subcutaneous tissue disordersCabozantinib118
otherAcute respiratory failureRespiratory, thoracic and mediastinal disordersCabozantinib118
otherAlanine aminotransferase increasedInvestigationsCabozantinib1418
otherAlkaline phosphatase increasedInvestigationsCabozantinib1118
otherAnemiaBlood and lymphatic system disordersCabozantinib718
otherAnorexiaMetabolism and nutrition disordersCabozantinib618
otherArthralgiaMusculoskeletal and connective tissue disordersCabozantinib118
otherAspartate aminotransferase increasedInvestigationsCabozantinib1318
otherBack painMusculoskeletal and connective tissue disordersCabozantinib318

Adverse event totals3

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityCabozantinib118
Total, other adverse eventsCabozantinib1818
Total, serious adverse eventsCabozantinib018

Papers1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed as
38608694DERIVED

Source PubMed

Grants1

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.

ProjectTitlePrincipal investigatorsOrganizationFunderFiscal years
P30CA016672The University of Texas MD Anderson Cancer Center Support Grant (CCSG)KOONG, ALBERTUNIVERSITY OF TX MD ANDERSON CAN CTRNATIONAL CANCER INSTITUTE1985 to 2026

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/NCT03370718

GET https://conductscience.org/api/trials/v1/NCT03370718/events?page=2