Drugs / SXC-2023

Trials 5

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 13 trials
Phase 1 NCT06343532 Oct → Dec 2024 substance-related disorder National Institute on Drug Abuse (NIDA) Completed No outcome recorded
Phase 1 NCT03542435 Apr → Aug 2018 — Promentis Pharmaceuticals, Inc. Completed No outcome recorded
Phase 1 NCT03301298 Sep 2017 → Feb 2018 — Promentis Pharmaceuticals, Inc. Completed No outcome recorded
Phase 22 trials
Phase 2 NCT03887429 Mar → Jul 2019 impulse control disorder Promentis Pharmaceuticals, Inc. Completed Mixed
Phase 2 NCT03797521 Dec 2018 → Dec 2019 trichotillomania Promentis Pharmaceuticals, Inc. Completed No outcome recorded

News releases announcing trial results or a regulatory action · 2

DateIssuerRelease
2019-10-31 Promentis Pharmaceuticals, Inc. Results Promentis Pharmaceuticals Announces Positive Results for Phase 2A Study of SXC-2023 Targeting Novel Glutamatergic Mechanism and Completion of Enrollment for Phase 2 Trichotillomania Study promentispharma.com ↗
The study reveals a clear effect associated with SXC-2023 administration in measures of impulse control closely related to trichotillomania and other indications of interest to the Company, and reinforces the attractive safety profile of SXC-2023.
2018-11-16 Promentis Pharmaceuticals, Inc. Results Promentis Pharmaceuticals Announces Successful Completion of Phase 1 Studies for SXC-2023 Targeting Novel Glutamatergic Mechanism promentispharma.com ↗
SXC-2023 proved to be safe and well-tolerated over a wide dose range in healthy volunteers in both the SAD and MAD studies, and demonstrated a very consistent PK profile.

Evidence & citations 2 cited values

Every value below carries the sentence it was read from. 5 sources stand behind the page.

FieldValueCited text
Known as SXC-2023 ClinicalTrials.gov intervention name — accepted as the source's own label NCT03797521 ↗
4

NCT03887429 ↗

NCT03542435 ↗

NCT03301298 ↗

NCT06343532 ↗

Route Oral “Single dose of 50 mg, given orally in capsule form.” NCT03301298 ↗