Sirolimus for Hydrocephalus

(VENTURE-PHH Trial)

KK
CF
Overseen ByCarla Fortes, BA
Age: 18+
Sex: Any
Trial Phase: Phase 1 & 2
Sponsor: Massachusetts General Hospital
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Breakthrough TherapyThis drug has been fast-tracked for approval by the FDA given its high promise

What You Need to Know Before You Apply

What is the purpose of this trial?

Hydrocephalus is a serious condition in which fluid builds up inside the brain, often requiring lifelong surgical placement of a shunt to drain excess cerebrospinal fluid (CSF). One of the most common causes of hydrocephalus is bleeding into the brain's fluid spaces after aneurysm rupture, prematurity, or infection. Currently, no medication exists to prevent hydrocephalus from developing after these injuries. The investigators' recent research suggests that hydrocephalus may result not only from blocked fluid pathways but also from harmful inflammation within the brain's ventricular system. The investigators discovered that inflammation activates the choroid plexus, the tissue that produces CSF, causing excessive CSF production and inflammatory injury to the ventricular lining and surrounding brain tissue. The investigators also identified inflammatory biomarkers and extracellular vesicles in human CSF that may enable real-time monitoring of these disease processes.

In this project, the investigators will perform a first-in-human pilot study testing whether targeted "intraventricular mTOR inhibition" can reduce ventricular inflammation and prevent hydrocephalus after severe brain hemorrhage. The medication will be delivered via temporary ventricular drains already in place as part of routine clinical care. The investigators will study safety, inflammation, CSF production, brain imaging changes, and whether patients ultimately require permanent shunts. Although this initial study focuses on adults with hemorrhage-related hydrocephalus, our long-term goal is to develop non-surgical therapies that could help children with hydrocephalus caused by prematurity or infection, especially in regions where access to neurosurgical care and shunt surgery is limited.

Who Is on the Research Team?

KK

Kristopher Kahle, MD, PhD

Principal Investigator

Massachusetts General Hospital

Are You a Good Fit for This Trial?

This trial is for adults who have developed hydrocephalus after a severe brain bleed and already have a temporary drain placed in their brain as part of standard care. People with other causes of hydrocephalus or without these drains are not eligible.

Inclusion Criteria

I am 18 years old or older.
I need an EVD as part of my standard neurocritical care.
Radiographic evidence of intraventricular hemorrhage (IVH)
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Exclusion Criteria

Pre-existing ventriculoperitoneal shunt dependence
I have a severely weakened immune system.
I cannot safely receive the study's heart treatment.
See 3 more

What Are the Treatments Tested in This Trial?

Interventions

  • Sirolimus (Rapamune®)

Trial Overview

The study is testing if giving the drug sirolimus (Rapamune) directly into the brain's fluid spaces through existing drains can reduce inflammation and prevent long-term fluid buildup (hydrocephalus) after a brain hemorrhage.

How Is the Trial Designed?

1

Treatment groups

Experimental Treatment

Group I: Ventricular mTOR Inhibition to Prevent Hydrocephalus After Brain HemorrhageExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Massachusetts General Hospital

Lead Sponsor

Trials
3,066
Recruited
13,430,000+