Clin2
NCT07767877Possibly a fitNot yet recruiting

Real-world study of medications for vascular anomalies

Vascular Anomalies

Part of Genetic & congenital, Heart & circulation clinical trials.

This study looks at how patients with vascular anomalies (abnormal blood vessel growths) respond to certain medications. It aims to gather real-world information about their care to improve future treatment.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
200 people
Ages
birth to 90 years
Study type
Observational

Who can take part

  • You have been diagnosed with a vascular anomaly (a condition involving abnormal blood vessels or lymph vessels).
  • You have been treated with one of the following types of medication for at least 3 months: mTOR inhibitors, MEK inhibitors, or PI3K inhibitors.
  • You do not have other rare genetic syndromes that complicate your health.
  • You have not been taking many other systemic medications that might make data collection difficult.
  • You have not used immunosuppressive drugs (medications that suppress the immune system) frequently, such as systemic steroids.
  • You are not currently enrolled in another clinical trial that involves an experimental treatment.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

Similar studies

Other trials that look related to this one.

NCT05983159Recruiting· Phase 2
Targeted therapy for slow-flow or fast-flow vascular malformations

This trial tests two targeted medicines for people with certain types of vascular malformations (abnormal blood vessels). If you have a slow-flow malformation, you may receive alpelisib; if you have a fast-flow malformation, you may receive mirdametinib. Genetic testing is needed to see if your malformation has a specific change that these drugs target.

Parkville, Victoria
NCT06789913Recruiting· Phase 2
Testing RLY-2608 for growth disorders linked to PIK3CA mutations

This trial tests a new medicine, RLY-2608, that targets the specific genetic change (PIK3CA mutation) causing overgrowth conditions. It aims to see if the drug can slow or stop the growth of affected tissues.

Phoenix, Arizona
NCT07477548Not yet recruiting· Phase 2
Testing everolimus for stubborn vascular anomalies

This trial tests the drug everolimus for people with certain types of vascular anomalies (tumors or malformations in blood vessels) that have not improved with other treatments. It aims to see if everolimus can help shrink these growths or control their symptoms.

NCT02638389Recruiting· Phase 3
Sirolimus for hard-to-treat vascular birthmarks

This Phase 3 study tests whether sirolimus helps control complex vascular anomalies that have not responded to standard treatments. It also checks safety by monitoring blood tests, organ function, and overall health during treatment.

Brussels, Brussels Capital
NCT07037238Recruiting· Phase 2
Everolimus for treating vascular malformations

This study tests a drug called everolimus to see if it helps treat vascular malformations (abnormal clusters of blood vessels). It is for adults aged 18 to 65 who have been diagnosed by MRI and are able to take oral medication.

Beijing
NCT03001180Recruiting
Study blood and tissue markers in vascular anomalies

This study collects extra blood (and sometimes tissue during procedures) to look for markers that can help doctors better understand vascular anomalies. It may not be a treatment, but it can improve future care by finding patterns linked to the condition.

Boston, Massachusetts

Hear when a new Vascular Anomalies trial opens

We’ll email you when one opens — at most once a week, no account needed, unsubscribe anytime.