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NCT06673368

A Phase 2 Randomized Double-Blind, Parallel, Adaptive-Design, Clinical Trial to Evaluate the Safety and Efficacy of NRCT-101SR With NRCT-202XR Compared to NRCT-202XR Alone in Subjects With Attention-Deficit/Hyperactivity Disorder

Terminated Phase 2 Last updated 15 January 2026
What this trial tests

Phase 2 trial testing NRCT-101SR, NRCT-202XR in ADHD in 2 participants. Terminated before completion.

Timeline
25 February 2025
Primary endpoint
15 July 2025
15 July 2025

Quick facts

Lead sponsorNeurocentria, Inc.
PhasePhase 2
StatusTerminated
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposetreatment
Enrollment2
Start date25 February 2025
Primary completion15 July 2025
Estimated completion15 July 2025
Sites5 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Neurocentria, Inc. — full company profile →

Who can join

Adults 13 to 17, any sex, with ADHD. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

A combination therapy of NRCT-101 with NRCT-202 is being developed for patients with ADHD.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for ADHD

Currently open trials in the same condition.

Other Neurocentria, Inc. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06673368.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing