Phase 2 Vasculitis Trial, Recruiting NCT02638701 Sponsor: University of California, San Francisco Condition: Vasculitis
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Phase 2 Vasculitis Trial, Recruiting

NCT02638701
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 who have a specific type of enlarged, widened artery (called a dolichoectatic aneurysm) in the back part of the brain that cannot be treated with surgery or other standard procedures.
  • People who are older than 18 years of age at the time the study treatment begins.

Who may not be able to join:

  • People who have taken certain immune-system-suppressing medications (such as abatacept, rituximab, tocilizumab, or similar "biologic" drugs) in the past 12 months.
  • People whose blood test results at the screening visit show too few white blood cells, too few platelets, low red blood cell levels, liver enzyme levels that are three or more times higher than normal, or poor kidney function.
  • People who test positive for tuberculosis (TB) exposure on a skin or blood test, unless there is documented proof that a full course of treatment or prevention treatment has been completed or is ongoing for at least 30 days. People with active TB infection are also excluded.
  • People who have a past history of a positive TB test or a chest X-ray suggesting prior TB, without records showing that TB treatment or preventive treatment was carried out.
  • People who currently have open sores or ulcers on their legs.
  • People who have a long-term or persistent infection, including HIV, untreated hepatitis B, listeria, TB, or other serious infections. (People with hepatitis C without serious liver damage, or those with chronic hepatitis B who are on antiviral treatment, may be considered on a case-by-case basis — confirm with the trial site.)
  • People who have had a serious active infection requiring hospital care or intravenous antibiotics, antivirals, or antifungal treatment in the 30 days before joining the trial, or who have taken oral antibiotics, antivirals, or antifungals in the 14 days before joining.
  • People who have received a live vaccine within 4 weeks before joining the trial.
  • People who have had a cancer diagnosis in the past 5 years, except for certain early-stage, localised skin cancers or cervical carcinoma in situ that have been fully treated.
  • People who, in the trial doctor's judgment, would face unacceptable risk by taking part in the study.
  • Women who are able to become pregnant, are sexually active, and do not agree to use an accepted form of contraception throughout the study (such as condoms, diaphragm, intrauterine device, oral or injected contraceptives started at least 2 months before the study drug, a vasectomised partner, or abstinence).
  • Women who are pregnant (a negative pregnancy blood test is required for all women who could potentially become pregnant) or who are currently breastfeeding.
  • People who have taken any other experimental drug or treatment within 4 weeks, or within 5 half-lives of that drug (whichever is earlier), before joining the trial.
  • People who have had a problem with drug or alcohol misuse in the 6 months before joining the trial.
  • People who have a known allergy or sensitivity to any of the study medications or products.
  • People who have a psychiatric condition that prevents them from being able to give informed consent to participate.
  • People who are unwilling or unable to follow the study requirements.
  • People who are unable to have an MRI scan.

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

Principal Investigator: Daniel L Cooke, MD, University of California, San Francisco

Phone: 415-353-1863

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
Registry
ClinicalTrials.gov
Start date
1 October 2024
Est. completion
1 June 2028

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Reduction in aneurysm volume (ml)

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