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Neurocentrx Pharma Limited is a private Scottish clinical-stage company developing NRCx-201 (Keticap) — an immediate-release, abuse-deterrent oral ketamine capsule paired with proprietary digital prescription safety software for regulated clinic-to-home care. Founded in 2013 by CEO Carmel Reilly at the University of Edinburgh, the company raised ~$6.15M total including a September 2025 seed extension (~$5M) led by the Wellcome Trust to fund a Phase 2 proof-of-concept trial in treatment-resistant bipolar depression (planned Q1 2026). Phase 1 (King's College London, EudraCT 2019-001019-22, n=18, 40–240mg) completed early 2023 with positive results: well-tolerated at all doses, no SAEs, PK comparable to IV/intranasal esketamine, no cognitive impairment. MHRA has indicated NRCx-201 is suitable for direct Phase 3 submission for TRD (company plans Phase 2 first). Key investors: Wellcome Trust, Neo Kuma Ventures, O2h Ventures, Equity Gap.

Development Programmes

1

NRCx-201 (Keticap)

Ketamine
Phase II

Treatment-resistant bipolar depression and TRD — immediate-release oral ketamine capsule with abuse-deterrent formulation + digital care combination

Programme Tracker

Treatment-Resistant Depression (TRD)

Primary: UK (MHRA)
Phase IIActive

Phase 2 PoC in treatment-resistant bipolar depression initiated Q1 2026 at King's College London, funded by Wellcome Trust (>$5M / £3.7M). Phase 1 full results published in Journal of Psychopharmacology (June 2025). Seeking Series A for separate Phase 2/3 MDD programme.

Milestones

Phase I topline

Completed

Actual: Oct 24, 2023

Positive Phase 1 top-line results announced — randomised, double-blind, placebo-controlled study at King's College London confirmed safety and tolerability of Keticap. PK profile comparable to IV ketamine and intranasal esketamine.

Why it matters: Phase 1 demonstrated that Keticap (oral IR ketamine with abuse-deterrent formulation) achieves plasma concentrations comparable to IV and intranasal routes. The abuse-deterrent design is the key differentiator — if effective, it could unlock primary care prescribing of ketamine for depression, which is currently limited by diversion concerns.

Watch next: Phase 2 efficacy data in bipolar depression

Phase I publication

Completed

Actual: Jun 1, 2025

Phase 1 full results published in Journal of Psychopharmacology (vol 39(6), pp 545-558). Investigators: Allan Young and Mario Juruena at King's College London.

Why it matters: Peer-reviewed publication validates the Phase 1 data and provides the scientific foundation for Phase 2 grant applications. The Wellcome Trust funding followed this publication.

Phase II started

Completed

Actual: Jan 1, 2026

Phase 2 proof-of-concept in treatment-resistant bipolar depression initiated at King's College London, funded by Wellcome Trust

Why it matters: Bipolar depression is notoriously difficult to treat — current options (lithium, quetiapine, lurasidone) have limited efficacy and significant side effects. Ketamine has shown rapid antidepressant effects in bipolar depression, but abuse/diversion risk limits prescribing. An abuse-deterrent oral formulation could change the risk-benefit calculus.

Watch next: Phase 2 PoC efficacy results; Series A for MDD Phase 2/3

Funding milestone

Completed

Actual: Sep 23, 2025

Closed seed extension round including >$5M (£3.7M) from Wellcome Trust

Why it matters: Wellcome Trust funding is highly competitive and validates the scientific rationale for abuse-deterrent oral ketamine. Provides non-dilutive capital for the Phase 2 bipolar depression study, reducing investor risk ahead of the Series A for the broader MDD programme.

Recorded Events

Jan 1, 2026: Phase II started

Sep 23, 2025: Funding milestone

Jun 1, 2025: Phase I publication

Oct 24, 2023: Phase I topline

Quick Facts

Type
Private Biotech
Lead Stage
Phase II
Website
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