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Trial · NCT05011396

PH94B Nasal Spray for Anxiety Induced by a Public Speaking Challenge - 2

NCT05011396, Phase 3, Terminated, VistaGen Therapeutics, Inc.; results first posted 2025-11-24

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. PH94B Nasal Spray for Anxiety Induced by a Public Speaking Challenge - 2. Trials, record NCT05011396. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT05011396

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Trial

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

Title
PH94B Nasal Spray for Anxiety Induced by a Public Speaking Challenge - 2
NCT number
NCT05011396
Status
Terminated
Phases
Phase 3
Enrollment
228 participants, actual
Lead sponsor
VistaGen Therapeutics, Inc.
Conditions
Social Anxiety Disorder
Interventions
PH94B Nasal Spray, Placebo Nasal Spray
First posted
2021-08-18
Last updated
2025-11-24
Results first posted
2025-11-24

Source ClinicalTrials.gov

Registered outcomes2

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

ListOutcomeTime frameDescription
PrimarySubjective Units of Distress Scale (SUDS)Visit 2 (Baseline; Day 0) to Visit 3 (Day 7 ± 2 days)
The SUDS is a patient self-rated scale that is scored in the range of 0 to 100 (operationalized for participants in this study as 0=totally relaxed or no anxiety and 100=highest distress or anxiety ever felt
SecondaryProportions (%) of CGI-I Responders in PH94B-treated and Placebo-treated Groups at the End of Visit 3 (Treatment)Visit 2 (Baseline; Day 0) to Visit 3 (Day 7 ± 2 days)
The CGI-I scale is a clinician-rated scale to assess illness improvement. The CGI-I scale includes one item scored from 1 (Very much less anxious) to 7 (Very much more anxious) with 4 being no change. Subjects are considered CGI-I responders with scores of 1 (Very much less anxious) or 2 (Much less anxious).

Outcomes2

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

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYSubjective Units of Distress Scale (SUDS)Visit 2 (Baseline; Day 0) to Visit 3 (Day 7 ± 2 days)score on a scaleMEAN
SECONDARYProportions (%) of CGI-I Responders in PH94B-treated and Placebo-treated Groups at the End of Visit 3 (Treatment)Visit 2 (Baseline; Day 0) to Visit 3 (Day 7 ± 2 days)ParticipantsCOUNT_OF_PARTICIPANTS

Results by group6

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

OutcomeGroupCategoryValueSpreadUnits
Subjective Units of Distress Scale (SUDS)PH94BVisit 278.6Standard Deviation 12.11score on a scale
Subjective Units of Distress Scale (SUDS)PlaceboVisit 282.2Standard Deviation 11.58score on a scale
Subjective Units of Distress Scale (SUDS)PH94BVisit 364.1Standard Deviation 17.05score on a scale
Subjective Units of Distress Scale (SUDS)PlaceboVisit 372.4Standard Deviation 15.82score on a scale
Proportions (%) of CGI-I Responders in PH94B-treated and Placebo-treated Groups at the End of Visit 3 (Treatment)PH94B26Participants
Proportions (%) of CGI-I Responders in PH94B-treated and Placebo-treated Groups at the End of Visit 3 (Treatment)Placebo15Participants

Participant flow6

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

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDPH94B70
Overall StudySTARTEDPlacebo71
Overall StudyCOMPLETEDPH94B67
Overall StudyCOMPLETEDPlacebo68
Overall StudyNOT COMPLETEDPH94B3
Overall StudyNOT COMPLETEDPlacebo3

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 totals9

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityBefore V3 Dosing0228
Total, all-cause mortalityPH94B070
Total, all-cause mortalityPlacebo070
Total, other adverse eventsBefore V3 Dosing0228
Total, other adverse eventsPH94B070
Total, other adverse eventsPlacebo070
Total, serious adverse eventsBefore V3 Dosing0228
Total, serious adverse eventsPH94B070
Total, serious adverse eventsPlacebo070

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 comparisons1

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

Comparison
PH94B vs Placebo: Proportions (%) of CGI-I Responders in PH94B-treated and Placebo-treated Groups at the End of Visit 3 (Treatment)

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/NCT05011396

GET https://conductscience.org/api/trials/v1/NCT05011396/registered