ConductScience.org, home

Trial · NCT04318145

Study to Evaluate Sex Differences in the Acute Effects of PL-3994 in Heart Failure Subjects

NCT04318145, Phase 2, Terminated, Palatin Technologies, Inc

3 sourcestrials-2026-11-12-0.5.0

Download JSON
Cite this record

ConductScience Library. Study to Evaluate Sex Differences in the Acute Effects of PL-3994 in Heart Failure Subjects. Trials, record NCT04318145. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04318145

On this page

Trial

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

Title
Study to Evaluate Sex Differences in the Acute Effects of PL-3994 in Heart Failure Subjects
NCT number
NCT04318145
Status
Terminated
Phases
Phase 2
Enrollment
15 participants, actual
Lead sponsor
Palatin Technologies, Inc
Conditions
Heart Failure With Preserved Ejection Fraction
Interventions
PL-3994 Aqueous Intravenous Solution Dose Ascention, PL-3994 Aqueous Intravenous Solution Single Dose
First posted
2020-03-23
Last updated
2025-12-15

Source ClinicalTrials.gov

Registered outcomes8

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

ListOutcomeTime frameDescription
PrimaryPart A: Dose Ascension1 dayReaching the maximum tolderated dose (MTD) as defined by meeting stopping criteria.
PrimaryPart B: Coronary Sinus Levels1 dayCoronary sinus levels of cGMP post PL-3994 infusion as compared to baseline.
SecondaryPart B: Blood pressure measured in mmHg1 dayMeasured at baseline (t=0) and at t=3, 6, 9, 12, and 15 minutes after the infusion of study drug.
SecondaryPart B: Heart rate measured in beats per minute1 dayMeasured at baseline (t=0) and at t=3, 6, 9, 12, and 15 minutes after the infusion of study drug.
SecondaryPart B: Right atrial pressure measured in mmHg1 dayMeasured at baseline (t=0) and at t=3, 6, 9, 12, and 15 minutes after the infusion of study drug.
SecondaryPart B: Pulmonary artery pressure measured in mmHg1 dayMeasured at baseline (t=0) and at t=3, 6, 9, 12, and 15 minutes after the infusion of study drug.
SecondaryPart B: Pulmonary capillary wedge pressure measured in mmHg1 dayMeasured at baseline (t=0) and at t=3, 6, 9, 12, and 15 minutes after the infusion of study drug.
SecondaryPart B: Cardiac output measured in L/min.1 dayMeasured at baseline (t=0) and at t=3, 6, 9, 12, and 15 minutes after the infusion of study drug.

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.

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/NCT04318145

GET https://conductscience.org/api/trials/v1/NCT04318145/registered