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Trial · NCT04635059

Pacritinib for Biochemical Relapse After Definitive Treatment for Prostate Cancer

NCT04635059, Phase 2, Terminated, Medical College of Wisconsin; results first posted 2024-12-17

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Pacritinib for Biochemical Relapse After Definitive Treatment for Prostate Cancer. Trials, record NCT04635059. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04635059

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Trial

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

Title
Pacritinib for Biochemical Relapse After Definitive Treatment for Prostate Cancer
NCT number
NCT04635059
Status
Terminated
Phases
Phase 2
Enrollment
6 participants, actual
Lead sponsor
Medical College of Wisconsin
Conditions
Prostate Cancer
Interventions
Pacritinib
First posted
2020-11-18
Last updated
2025-11-17
Results first posted
2024-12-17

Source ClinicalTrials.gov

Registered outcomes3

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

ListOutcomeTime frameDescription
PrimaryThe Number of Patients With Six-month PSA Progression-free Survival.Six monthsPSA progression-free survival is defined as the length of time that a subject will be alive and free from PSA progression per PCWG3 guidelines.
SecondaryPSA LevelsCycle1Day1 (month 0), every month up to month 4.PSA level in blood is measured in units of nanograms per milliliter.
SecondaryTestosterone MeasurementBaseline and three monthsSerum testosterone will be measured in nanograms per deciliter.

Outcomes3

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYThe Number of Patients With Six-month PSA Progression-free Survival.Six monthsParticipantsCOUNT_OF_PARTICIPANTS
SECONDARYPSA LevelsCycle1Day1 (month 0), every month up to month 4.Two subjects were not tested in month 4.ng/mLMEAN
SECONDARYTestosterone MeasurementBaseline and three monthsTwo subjects were not tested in month 3.ng/dLMEAN

Results by group8

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

OutcomeGroupCategoryValueSpreadUnits
The Number of Patients With Six-month PSA Progression-free Survival.Pacritinib0Participants
PSA LevelsPacritinibPSA at C1D1 (month 0), ng/mL1.9Standard Deviation .5ng/mL
PSA LevelsPacritinibPSA at month 1, ng/mL3.2Standard Deviation .8ng/mL
PSA LevelsPacritinibPSA at month 2, ng/mL4.1Standard Deviation 1.3ng/mL
PSA LevelsPacritinibPSA at month 3, ng/mL4.7Standard Deviation .8ng/mL
PSA LevelsPacritinibPSA at month 4, ng/mL5.7Standard Deviation .3ng/mL
Testosterone MeasurementPacritinibTestosterone at screening, ng/dL390Standard Deviation 280ng/dL
Testosterone MeasurementPacritinibTestosterone at 3 months, ng/dL330Standard Deviation 181ng/dL

Participant flow3

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDPacritinib6
Overall StudyCOMPLETEDPacritinib2
Overall StudyNOT COMPLETEDPacritinib4

Adverse events56

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

TypeEventOrgan systemGroupAffectedAt riskEvents
otherAlanine aminotransferase increasedInvestigationsPacritinib162
otherAlkaline phosphatase increasedInvestigationsPacritinib161
otherAllergic rhinitisRespiratory, thoracic and mediastinal disordersPacritinib161
otherAnorexiaMetabolism and nutrition disordersPacritinib161
otherArthralgiaMusculoskeletal and connective tissue disordersPacritinib161
otherAspartate aminotransferase increasedInvestigationsPacritinib161
otherAtrial fibrillationCardiac disordersPacritinib161
otherBack painMusculoskeletal and connective tissue disordersPacritinib262
otherBladder spasmRenal and urinary disordersPacritinib161
otherBelchingGastrointestinal disordersPacritinib161

Adverse event totals3

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityPacritinib06
Total, other adverse eventsPacritinib66
Total, serious adverse eventsPacritinib06

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/NCT04635059

GET https://conductscience.org/api/trials/v1/NCT04635059/events?page=2