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AQST US Equity

Aquestive Therapeutics, Inc.Health Care · Pharmaceutical Preparations · CIK 1398733 · FY ends Dec 31
$4.59
+0.27 (+6.25%)
USD · as of 2026-08-19 · marketstack
9 registered studies · 0 active

Studies where AQST is the lead sponsor, as filed with ClinicalTrials.gov. Completion dates are the sponsor's own projected windows and are revised as a study runs. Active studies first, then completed and stopped — newest readout first within each.

9 interventional · 6 with posted results

Held by 14 tracked-famous managers (TWO SIGMA INVESTMENTS, LP, Balyasny Asset Management L.P., CITADEL ADVISORS LLC, JANE STREET GROUP, LLC, RENAISSANCE TECHNOLOGIES LLC, +9 more) · FINRA short interest 8.9 days to cover (settled 2026-07-31) · insider 90d: 0 buys / 2 sells · government filings 180d: none disclosed

StudyPhaseStatusInterventionsConditionsEnrollmentPrimary completionUpdated
A Study to Evaluate the Pharmacokinetics, Pharmacodynamics, and Safety of DESF in Pediatric SubjectsNCT07703982CmaxOpen-label · TreatmentPhase 1CompletedDrug: DESFAllergic Reaction322025-03-14actual2026-07-15
Pharmacokinetics Study of DESF in Adults With Oral Allergy SyndromeNCT06527937CmaxRandomized · Open-label · TreatmentPhase 2CompletedDrug: DESF, Epinephrine InjectionAllergic Reaction362024-10-10actual2025-09-26
Safety and Tolerability Study of Diazepam Buccal Film (DBF) in Subjects With EpilepsyNCT03428360results2021-08-05Number of Subjects in the Safety Analysis Set With at Least 1 Treatment-emergent Adverse Event (TEAE)Open-label · TreatmentStudy Protocol · Statistical Analysis PlanPhase 3CompletedDrug: Diazepam Buccal Soluble Film 5, 7.5,10, 12.5,15 or 17.5 mg with individual dose determined according to age and weight categoryEpilepsy1492020-06-25actual2021-08-05
Pharmacokinetics and Safety Study of Diazepam Buccal Film (DBF) in Pediatric Subjects With EpilepsyNCT03222349results2021-05-26Area Under the Concentration Time Curve (AUC) 0 to 4 Hours Post-doseNon-randomized · Open-label · TreatmentStudy Protocol · Statistical Analysis PlanPhase 2CompletedDrug: Diazepam Buccal FilmEpilepsy242020-01-28actual2021-05-26
Diazepam Buccal Film (DBF) - Diastat Rectal Gel (DRG) Crossover StudyNCT03953820results2020-08-18AUC 0-tRandomized · Open-label · TreatmentStudy Protocol · Statistical Analysis PlanPhase 1/2CompletedDrug: Diazepam Buccal Film, Diastat® Rectal Gel (Valeant Pharmaceuticals USA)Epilepsy312019-07-31actual2020-08-18
Riluzole Oral Soluble Film (ROSF) Swallowing Safety in Amyotrophic Lateral Sclerosis (ALS)NCT03679975results2020-08-10Number of Participants Categorized by Differences From Baseline in Penetration Aspiration Scale (PAS) - Sum of Scores MethodOpen-label · OtherStudy Protocol · Statistical Analysis PlanPhase 2Terminatedsponsor's stated reason: The study is no longer requiredDrug: Riluzole Oral Soluble film (ROSF) 50 mgAmyotrophic Lateral Sclerosis92018-09-26actual2020-08-18
Study of Diazepam Buccal Film Administered in the Interictal and in the Ictal-Periictal States to Adults With EpilepsyNCT03179891results2020-09-18Tmax Pharmacokinetic EndPointsNon-randomized · Open-label · TreatmentStudy Protocol · Statistical Analysis PlanPhase 2CompletedDrug: Diazepam Buccal Film 12.5 mgEpilepsy352018-07-25actual2020-09-18
Riluzole Oral Soluble Film Safety and Tolerability in Amyotrophic Lateral SclerosisNCT03457753Change from baseline in NCI-CTC score at week 12Open-label · OtherPhase 2Withdrawnsponsor's stated reason: The Sponsor stopped the study due to a change in study plansDrug: Riluzole Oral Soluble FilmALS02018-03-27actual2019-05-13
Three-way Crossover Study Comparing Ondansetron ODFS Administered With and Without Water to Zofran ODT Without WaterNCT01220167results2020-08-18CmaxRandomized · Open-label · OtherPhase 1CompletedDrug: Ondansetron 8 mg ODFS without water, Ondansetron 8 mg ODFS with water, Zofran ODT (ondansetron 8 mg) without waterHealthy Participants18Aug 2008actual2020-08-18

Primary completion is the date the sponsor filed with the registry — their own projection, revised whenever they revise it, unless the row is marked actual.

Source: ClinicalTrials.gov, retrieved 2026-08-19