Phase 3 Osteoarthritis Trial, Recruiting NCT07509307 Sponsor: Novo Nordisk A/S Condition: Osteoarthritis
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Phase 3 Osteoarthritis Trial, Recruiting

NCT07509307
Recruiting Phase 3 🇦🇺 Australian site

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 were male or female at birth, aged 18 or older at the time of signing the consent form
  • People who have been clinically diagnosed with knee osteoarthritis and have confirmed changes visible on X-ray in the knee being studied (rated at a certain level of severity by a central reviewer)
  • People whose knee osteoarthritis pain in the target knee first appeared more than 90 days before the screening visit, and who had pain on more than 15 days out of the past 30 days
  • People who are willing to stop taking most pain relief medications for 72 hours before certain study visits (a limited amount of paracetamol is allowed up until 24 hours before those visits)

Who may not be able to join:

  • People whose blood sugar marker (HbA1c) is measured at 6.5% or above in the screening blood test
  • People who have a history of type 1 or type 2 diabetes, either as reported by themselves or recorded in their medical history
  • People who have previously been treated with a class of medications known as GLP-1 receptor agonists, dual GLP-1/GIP receptor agonists, or amylin analogues (confirm with trial site if unsure whether a current or past medication falls into these categories)
  • People who have an artificial joint or joint replacement in the knee being studied
  • People who have had a knee scope procedure (arthroscopy) or an injection into the target knee within the 90 days before screening
  • People who have any other joint condition affecting the target knee, including gout or pseudogout

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 14 July 2026
Phase 3: approximately ~65% 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

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

Phone: (+1) 866-867-7178

Australian sites

Emeritus Research Sydney, Botany, New South Wales
Momentum Clinical Research Darlinghurst, Darlinghurst, New South Wales
Kolling Institute, St Leonards, New South Wales
Heart of Australia, Chelmer, Queensland
Coastal Digestive Health, Maroochydore, Queensland

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 3
Registry
ClinicalTrials.gov
Start date
20 April 2026
Est. completion
14 August 2028

Where this trial is recruiting

🇦🇺 Australia 🇧🇬 Bulgaria 🇨🇦 Canada 🇩🇰 Denmark 🇬🇷 Greece 🇮🇹 Italy 🇵🇱 Poland Puerto Rico 🇪🇸 Spain Turkey (Türkiye) 🇺🇸 United States

5 site(s) in Australia. Confirm current status and contact details directly with the trial site.

Primary endpoints

Relative change in body weight; Change in Western Ontario and McMaster Universities Osteoarthritis Index Numerical Rating Scale (NRS) 3.1 (24-hour) (WOMAC) pain score

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: 14 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