Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
Biomarker and Edema Attenuation in IntraCerebral Hemorrhage (BEACH)
NCT05020535 · View on ClinicalTrials.gov ↗
Study Summary
This first-in-patient phase 2a pilot study will assess the safety and tolerability of MW01-6-189WH (hereafter called MW189) in patients with Intracerebral Hemorrhage (ICH).
Conditions Studied
Interventions
- OTHER Saline
- DRUG MW189
Study Locations (11)
Texas
- University of Texas Houston — Houston
- University of Texas San Antonio — San Antonio
Alabama
- University of Alabama Birmingham — Birmingham
California
- Stanford University — Palo Alto
Connecticut
- Yale New Haven Hospital — New Haven
Florida
- Cleveland Clinic Florida — Stuart
Kentucky
- University of Kentucky — Lexington
Maryland
- Johns Hopkins Hospital — Baltimore
New Mexico
- University of New Mexico — Albuquerque
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 120 participants |
| Start Date | 2022-10-10 |
| Est. Completion | 2027-10-01 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05020535
The ClinicalTrials.gov registry entry for NCT05020535 describes a study currently listed as recruiting. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 120 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Johns Hopkins University, which has 1,517 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Intracerebral Hemorrhage appearing as the primary indexed condition, and to 2 interventions — of which Saline is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT05020535 reports 11 study locations spanning 10 distinct geographic areas — top geographies include Texas, Alabama, California. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT05020535 about?
NCT05020535 is a clinical study titled "Biomarker and Edema Attenuation in IntraCerebral Hemorrhage (BEACH)". This first-in-patient phase 2a pilot study will assess the safety and tolerability of MW01-6-189WH (hereafter called MW189) in patients with Intracerebral Hemorrhage (ICH).
What is the current status of trial NCT05020535?
This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 120 participants. The study started on 2022-10-10. Estimated completion is 2027-10-01.
What conditions does trial NCT05020535 study?
This clinical trial studies the following conditions: Intracerebral Hemorrhage. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT05020535?
The interventions under investigation include: Saline (OTHER), MW189 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT05020535?
This trial is sponsored by Johns Hopkins University, which has 1,517 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT05020535 being conducted?
This trial has 11 study locations across Alabama, California, Connecticut, Florida, Kentucky. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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