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For investigators and research teams. See what NWPharmaTech has published about the CHR-P programme, with sources and limitations, build an agenda of points to discuss, and prepare a brief. No account is needed to explore the information or prepare a brief.

  1. Your focus (optional)
  2. Public information
  3. Agenda and brief
  4. Contact

The agenda, brief and online enquiry need JavaScript. Every card and its sources are listed below, and research collaboration enquiries can be made through the Contact page.

2 Relevant public information

Each card is taken from the Programme Room and the Evidence library, with its sources and limitations. Company statements and your own questions are always kept apart.

Clinical need and existing evidence

What published research says about people at clinical high risk of psychosis.

  • Finding NWPharmaTech public information

    An updated meta-analysis estimated that about one in four people identified as CHR-P (pooled estimate, 25%) developed psychosis within three years.

    Related stage: Stage 1 · Clinical need — stage work status: Background

    Sources and limitations (1)
    1. Salazar de Pablo et al. — probability of transition to psychosis (updated meta-analysis), JAMA Psychiatry

      Source type
      Published research
      Relates to
      The CHR-P field — no specific medicine
      Source date
      Published 2021
      Limitations
      The pooled estimate and the separate Kaplan–Meier series are different analyses and are not combined. Estimates span services and criteria; individual risk varies.
  • Limitation NWPharmaTech public information

    The pooled estimate and the separate Kaplan–Meier series are different analyses and are not combined. Estimates span services and criteria; individual risk varies.

    Related stage: Stage 1 · Clinical need — stage work status: Background

    Sources and limitations (1)
    1. Salazar de Pablo et al. — probability of transition to psychosis (updated meta-analysis), JAMA Psychiatry

      Source type
      Published research
      Relates to
      The CHR-P field — no specific medicine
      Source date
      Published 2021
      Limitations
      The pooled estimate and the separate Kaplan–Meier series are different analyses and are not combined. Estimates span services and criteria; individual risk varies.
  • Finding NWPharmaTech public information

    In England, psychological therapy is the recommended first step. NICE advises against antipsychotics to prevent psychosis in this group.

    Related stage: Stage 1 · Clinical need — stage work status: Background

    Sources and limitations (2)
    1. NICE CG155 — psychosis and schizophrenia in children and young people

      Source type
      Published guidance
      Relates to
      The CHR-P field — no specific medicine
      Source date
      Published 23 January 2013; last updated 26 October 2016
      Limitations
      Applies in England; guidance differs elsewhere.
    2. NICE CG178 — psychosis and schizophrenia in adults

      Source type
      Published guidance
      Relates to
      The CHR-P field — no specific medicine
      Source date
      Published 12 February 2014; last updated 4 September 2026
      Limitations
      Applies in England; guidance differs elsewhere.
  • Finding NWPharmaTech public information

    No preventive intervention has been shown to work better than the others.

    Related stage: Stage 1 · Clinical need — stage work status: Background

    Sources and limitations (1)
    1. Davies et al. — network meta-analysis of preventive interventions, World Psychiatry

      Source type
      Published research
      Relates to
      The CHR-P field — no specific medicine
      Source date
      Published 2018
      Limitations
      Few, small trials per intervention.

Formulation and absorption

What is known about giving cannabidiol by mouth, and about the NWPT-SM32300 softgel.

  • Finding NWPharmaTech public information

    Cannabidiol dissolves poorly in water. Taken by mouth while fasting, only about 6% of a dose is estimated to reach the bloodstream, and food changes absorption markedly (research on other CBD products).

    Related stage: Stage 2 · Formulation — stage work status: Completed

    Sources and limitations (2)
    1. Perucca and Bialer — oral cannabidiol bioavailability (review), CNS Drugs

      Source type
      Published research
      Relates to
      Other CBD products — not NWPT-SM32300
      Source date
      Published 2020
      Limitations
      Review of other CBD preparations; figures vary between studies.
    2. Taylor et al. — Phase 1 study of purified CBD, including a food-effect arm, CNS Drugs

      Source type
      Published research
      Relates to
      Other CBD products — not NWPT-SM32300
      Source date
      Published 2018
      Limitations
      Healthy volunteers; a different CBD product. A published correction exists.
  • Finding NWPharmaTech public information

    NWPT-SM32300 is a 300 mg softgel whose contents are designed to disperse into very small droplets in the gut.

    Related stage: Stage 2 · Formulation — stage work status: Completed

    Sources and limitations (1)
    1. Science — what is known and what remains open

      Source type
      Company records
      Relates to
      NWPT-SM32300 programme
      Source date
      No separate issue date (company web page)
      Website page last updated
      22 September 2026 (site map record; no review date is shown on the page)
      Limitations
      Summarises the questions; not a result.
  • Limitation NWPharmaTech public information

    Whether this formulation gives more consistent absorption than other CBD products. Phase 1 measured absorption; its results have not been published. How much reaches the brain has not been measured.

    Related stage: Stage 2 · Formulation — stage work status: Completed

    Sources and limitations (2)
    1. Phase 1 registration: NCT07186283 and ISRCTN25163383

      Source type
      Registry information
      Relates to
      NWPT-SM32300 programme
      Source date
      Registered 2025; exact registration date not available
      Limitations
      Healthy volunteers and single doses: measures absorption and short-term tolerability, not effectiveness in clinical high risk of psychosis.
    2. Science — what is known and what remains open

      Source type
      Company records
      Relates to
      NWPT-SM32300 programme
      Source date
      No separate issue date (company web page)
      Website page last updated
      22 September 2026 (site map record; no review date is shown on the page)
      Limitations
      Summarises the questions; not a result.

The Phase 1 study

The completed study in healthy volunteers, and what it can and cannot show.

  • Finding NWPharmaTech public information

    14 healthy adult volunteers; randomised, open-label, three-period crossover.

    Related stage: Stage 3 · Phase 1 — stage work status: Completed

    Sources and limitations (1)
    1. Phase 1 registration: NCT07186283 and ISRCTN25163383

      Source type
      Registry information
      Relates to
      NWPT-SM32300 programme
      Source date
      Registered 2025; exact registration date not available
      Limitations
      Healthy volunteers and single doses: measures absorption and short-term tolerability, not effectiveness in clinical high risk of psychosis.
  • Limitation NWPharmaTech public information

    Study activity ended on 10 December 2025. Results have not yet been published.

    Related stage: Stage 3 · Phase 1 — stage work status: Completed

    Sources and limitations (2)
    1. Phase 1 registration: NCT07186283 and ISRCTN25163383

      Source type
      Registry information
      Relates to
      NWPT-SM32300 programme
      Source date
      Registered 2025; exact registration date not available
      Limitations
      Healthy volunteers and single doses: measures absorption and short-term tolerability, not effectiveness in clinical high risk of psychosis.
    2. Study progress — Phase 1 milestones

      Source type
      Company records
      Relates to
      NWPT-SM32300 programme
      Record dates
      27 August 2025 to 30 March 2026
      Website page reviewed
      23 September 2026
      Limitations
      Database lock and analysis dates come from NWPharmaTech records (not published).
  • Limitation NWPharmaTech public information

    Healthy volunteers and single doses: measures absorption and short-term tolerability, not effectiveness in clinical high risk of psychosis.

    Related stage: Stage 3 · Phase 1 — stage work status: Completed

    Sources and limitations (1)
    1. Phase 1 registration: NCT07186283 and ISRCTN25163383

      Source type
      Registry information
      Relates to
      NWPT-SM32300 programme
      Source date
      Registered 2025; exact registration date not available
      Limitations
      Healthy volunteers and single doses: measures absorption and short-term tolerability, not effectiveness in clinical high risk of psychosis.

The planned Phase 2B study

Proposed research: its aims and current status.

  • Finding NWPharmaTech public information

    If it goes ahead: whether NWPT-SM32300 shows a dose response, changes symptoms, and is safe and tolerable in people at clinical high risk of psychosis.

    Related stage: Stage 5 · Phase 2B — stage work status: Proposed

    Sources and limitations (1)
    1. Study progress — current stage, aims and oversight

      Source type
      Company records
      Relates to
      NWPT-SM32300 programme
      Source date
      NWPharmaTech, September 2026
      Website page reviewed
      23 September 2026
      Limitations
      Phase 2B oversight arrangements not yet published.
  • Finding NWPharmaTech public information

    Status: planned. Not recruiting. The protocol is being finalised.

    Related stage: Stage 5 · Phase 2B — stage work status: Proposed

    Sources and limitations (2)
    1. Study progress — current stage, aims and oversight

      Source type
      Company records
      Relates to
      NWPT-SM32300 programme
      Source date
      NWPharmaTech, September 2026
      Website page reviewed
      23 September 2026
      Limitations
      Phase 2B oversight arrangements not yet published.
    2. Study progress — Phase 2B protocol finalisation (in progress)

      Source type
      Company records
      Relates to
      NWPT-SM32300 programme
      Record date
      23 February 2026 (as reported)
      Website page reviewed
      23 September 2026
      Limitations
      Company record; not published.
  • Finding NWPharmaTech public information

    The Phase 2B study can start only after regulatory and research ethics approval.

    Related stage: Stage 5 · Phase 2B — stage work status: Proposed

    Sources and limitations (1)
    1. Study progress — current stage, aims and oversight

      Source type
      Company records
      Relates to
      NWPT-SM32300 programme
      Source date
      NWPharmaTech, September 2026
      Website page reviewed
      23 September 2026
      Limitations
      Phase 2B oversight arrangements not yet published.
  • Limitation NWPharmaTech public information

    Oversight arrangements for the Phase 2B study have not yet been published.

    Related stage: Stage 5 · Phase 2B — stage work status: Proposed

    Sources and limitations (1)
    1. Study progress — current stage, aims and oversight

      Source type
      Company records
      Relates to
      NWPT-SM32300 programme
      Source date
      NWPharmaTech, September 2026
      Website page reviewed
      23 September 2026
      Limitations
      Phase 2B oversight arrangements not yet published.
  • Finding NWPharmaTech public information

    A larger UK trial of cannabidiol in this group (CANTOP-RCT) did not start owing to challenges in securing supply of the study drug, which is one reason this question remains open.

    Related stage: Stage 5 · Phase 2B — stage work status: Proposed

    Sources and limitations (1)
    1. Bhattacharyya S, Davies C, et al. — Cannabidiol as a treatment for patients who are clinically at high risk of developing psychosis: learnings from the CANTOP-RCT, NIHR Journals Library

      Source type
      Published research
      Relates to
      Other CBD products — not NWPT-SM32300
      Source date
      Published March 2025 (NIHR Journals Library PDF and PubMed record)
      Journal citation
      Efficacy Mech Eval 2026;13(7):197–214 (recommended citation on the current NIHR PDF)
      Limitations
      Produced no efficacy results; included to explain why a larger trial is still missing.
  • Limitation NWPharmaTech public information

    A small 21-day study of another CBD product in this group was published in 2024. Its findings are early, have not been confirmed in a larger trial, and do not apply directly to NWPT-SM32300.

    Related stage: Stage 5 · Phase 2B — stage work status: Proposed

    Sources and limitations (1)
    1. Bhattacharyya et al. — 21-day symptom study of another CBD product in clinical high risk, World Psychiatry

      Source type
      Published research
      Relates to
      Other CBD products — not NWPT-SM32300
      Source date
      Published 2024
      Limitations
      Very small, three weeks, short-letter format; not yet confirmed in a larger trial.

Open questions

What is not yet known.

  • Open question Unresolved NWPharmaTech public information

    Does NWPT-SM32300 reduce symptoms in people at clinical high risk?

    Not established. It would take the results of a pre-specified clinical study such as the planned Phase 2B.

    Related stage: Stage 5 · Phase 2B — stage work status: Proposed

    Sources and limitations (2)
    1. Study progress — current stage, aims and oversight

      Source type
      Company records
      Relates to
      NWPT-SM32300 programme
      Source date
      NWPharmaTech, September 2026
      Website page reviewed
      23 September 2026
      Limitations
      Phase 2B oversight arrangements not yet published.
    2. Bhattacharyya et al. — 21-day symptom study of another CBD product in clinical high risk, World Psychiatry

      Source type
      Published research
      Relates to
      Other CBD products — not NWPT-SM32300
      Source date
      Published 2024
      Limitations
      Very small, three weeks, short-letter format; not yet confirmed in a larger trial.
  • Open question Unresolved NWPharmaTech public information

    Is there a dose response, and which dose would be best?

    Not established. Dose response is one of the planned study’s aims.

    Related stage: Stage 5 · Phase 2B — stage work status: Proposed

    Sources and limitations (1)
    1. Study progress — current stage, aims and oversight

      Source type
      Company records
      Relates to
      NWPT-SM32300 programme
      Source date
      NWPharmaTech, September 2026
      Website page reviewed
      23 September 2026
      Limitations
      Phase 2B oversight arrangements not yet published.
  • Open question Unresolved NWPharmaTech public information

    Is it safe and well tolerated in this population?

    Not established. Phase 1 involved healthy volunteers and single doses only.

    Related stage: Stage 3 · Phase 1 — stage work status: Completed

    Sources and limitations (1)
    1. Phase 1 registration: NCT07186283 and ISRCTN25163383

      Source type
      Registry information
      Relates to
      NWPT-SM32300 programme
      Source date
      Registered 2025; exact registration date not available
      Limitations
      Healthy volunteers and single doses: measures absorption and short-term tolerability, not effectiveness in clinical high risk of psychosis.
  • Open question Unresolved NWPharmaTech public information

    How much reaches the brain?

    No study has measured it.

    Related stage: Stage 2 · Formulation — stage work status: Completed

    Sources and limitations (1)
    1. Science — what is known and what remains open

      Source type
      Company records
      Relates to
      NWPT-SM32300 programme
      Source date
      No separate issue date (company web page)
      Website page last updated
      22 September 2026 (site map record; no review date is shown on the page)
      Limitations
      Summarises the questions; not a result.
  • Open question Unresolved NWPharmaTech public information

    Can transition to psychosis be delayed or prevented?

    A longer-term question needing a separately powered trial with long follow-up.

    Related stage: Stage 6 · Longer term — stage work status: Open question

    Sources and limitations (1)
    1. Davies et al. — network meta-analysis of preventive interventions, World Psychiatry

      Source type
      Published research
      Relates to
      The CHR-P field — no specific medicine
      Source date
      Published 2018
      Limitations
      Few, small trials per intervention.

Exploring a collaboration

What this page can and cannot do, and questions you may want to raise.

  • Website statement NWPharmaTech public information

    This page brings together public information to help you prepare a conversation. It does not offer a study protocol, study medicine, sponsorship, funding or access to unpublished data. Selecting a card does not commit you or NWPharmaTech to anything.

  • Question for discussion Suggested wording for your question

    How does my research question relate to the aims of the planned Phase 2B study?

  • Question for discussion Suggested wording for your question

    Who could discuss methods or study-design questions with me?

  • Question for discussion Suggested wording for your question

    When are the Phase 1 results expected to be published?

  • Question for discussion Suggested wording for your question

    What should a collaboration enquiry include so that NWPharmaTech can consider it?

4 Contact about collaboration

Please do not include confidential or unpublished information, patient information or health data. This is not a diagnosis service, crisis line, or trial enrolment portal.

Online enquiries need JavaScript. To contact us about a research collaboration, email [email protected] with the subject “Research collaboration”, or see the Contact page.

Content version wwu-1 · public information reviewed 26 September 2026. Sources come from the Evidence library and the study records. See the privacy notice.

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