Phase 2 Gout Trial, Recruiting NCT07535034 Sponsor: Crystalys Therapeutics Condition: Gout
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Phase 2 Gout Trial, Recruiting

NCT07535034
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:

  • You are between 18 and 75 years old (inclusive) at the time of signing the consent form.
  • You have been diagnosed with gout (based on specific medical guidelines) for at least 1 year, AND either you have had problems tolerating or been advised against taking allopurinol or febuxostat, OR a previous uricase treatment did not work well enough or caused problems for you.
  • Your uric acid level in your blood is above 6.0 and below 10.5 mg/dL, confirmed at two separate screening appointments.
  • If you are a woman who could become pregnant, you must have a negative pregnancy test at two points during screening and must not be breastfeeding.
  • If you could father or become pregnant, you must agree to either abstain from heterosexual sex or use an acceptable form of birth control from signing the consent form until 30 days after your last dose of the trial drug.

Who may not be able to join:

  • You have had kidney stones within the past year.
  • You have had a cancer diagnosis in the last 5 years, except for certain treated skin cancers (basal or squamous cell carcinoma).
  • You have a known history of drug misuse, tested positive for drugs at the first screening visit, or have a recent history of alcohol misuse.
  • You have HIV, Hepatitis B, or Hepatitis C, or tested positive for these during screening.
  • You have any significant health condition that, in the trial doctor's opinion, could affect your safety, your ability to follow the trial requirements, or the accuracy of the trial results (confirm with trial site).

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: (858) 356-4740

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
Crystalys Therapeutics
Registry
ClinicalTrials.gov
Start date
8 May 2026
Est. completion
1 July 2027

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Percentage of Participants With an sUA Level <6.0 mg/dL at Week 24

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