Type 1 Diabetes Trial, Recruiting NCT06807190 Sponsor: Novo Nordisk A/S Condition: Type 1 Diabetes
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Type 1 Diabetes Trial, Recruiting

NCT06807190
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People who have given signed consent before any study-related activities begin.
  • People for whom the treating doctor and the patient (or their legal representative) have already decided — independently from this study — to start treatment with the commercially available medication Awiqli.
  • People of any age, male or female.
  • People who have been diagnosed with diabetes mellitus, with no restrictions on the type of diabetes or previous diabetes treatments.

Who may not be able to join:

  • People who have previously taken part in this same study by giving informed consent.
  • People who have taken part in another clinical trial involving an experimental drug within the 30 days before joining this study.
  • People who, due to mental capacity, unwillingness, or language barriers, are unable to adequately understand or cooperate with the study.
  • People for whom this medication is listed as not suitable (contraindicated) according to the official Japanese prescribing information.
  • People who are currently experiencing symptoms of low blood sugar (hypoglycaemia).
  • People who have had an allergic reaction to any ingredient in this medication in the past.

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 15 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Clinical Transparency (dept. 2834), Novo Nordisk A/S

Phone: (+1) 866-867-7178

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Registry
ClinicalTrials.gov
Start date
15 April 2025
Est. completion
31 July 2027

Where this trial is recruiting

🇯🇵 Japan

Primary endpoints

Number of Adverse Reactions (ARs)

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 15 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov