Phase 2 Type 1 Diabetes Trial, Recruiting NCT06700538 Sponsor: Arrowhead Pharmaceuticals Condition: Type 1 Diabetes
Back to Type 1 Diabetes

Phase 2 Type 1 Diabetes Trial, Recruiting

NCT06700538
Recruiting Phase 2

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 with obesity, meaning a Body Mass Index (BMI) between 30 and 50 kg/m², as measured at the screening appointment.
  • People who have tried at least once to lose weight through lifestyle changes (such as diet and exercise) without success.
  • People who have had Type 2 diabetes for at least 6 months before screening, with blood sugar levels (HbA1c) in a specific range (6.0%–9.5%), and who have been on a stable diabetes medication routine for at least 3 months — this applies to certain parts of the trial only (confirm with trial site).
  • People who are willing and able to follow all study requirements, including keeping to a stable diet and exercise routine for the whole duration of the trial.
  • People who have no significant abnormal health findings at screening that could affect their safety or the study results, as judged by the study doctor.
  • People of childbearing potential who agree to use highly effective contraception during the study and for at least 90 days after the study ends or the last dose of study medication (whichever is later), and who agree not to donate sperm or eggs during that same period.

Who may not be able to join:

  • People who have lost or gained more than 5% of their body weight in the 3 months before screening.
  • People who have used GLP-1 receptor agonist medications (such as liraglutide or semaglutide) for any reason in the 6 months before screening.
  • People who have used other prescription or over-the-counter weight loss medications or supplements (such as naltrexone/bupropion, orlistat, or phentermine/topiramate) in the 3 months before screening.
  • People whose obesity is considered by the study doctor to be caused by a medication, a single-gene condition, or a hormonal disorder (conditions other than polycystic ovary syndrome).
  • People who have previously had surgery or a medical device used to treat obesity.
  • People who have used medications strongly linked to weight gain in the 3 months before screening.
  • People with Type 1 diabetes.
  • People with a history of an overactive thyroid, or whose thyroid hormone levels fall outside a specific range at screening.
  • People with significant disease affecting major organs (confirm with trial site for specific details).

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 28 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Phone: 626-304-3400

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
Phase 2
Sponsor
Arrowhead Pharmaceuticals
Registry
ClinicalTrials.gov
Start date
4 December 2024
Est. completion
17 September 2027

Where this trial is recruiting

🇳🇿 New Zealand

Primary endpoints

Number of Participants with Treatment-Emergent Adverse Events (TEAEs)

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: 28 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