A Pilot Study of Minocycline in Intracerebral Hemorrhage Patients

MACH is a randomized trial of minocycline in intracerebral hemorrhage. 24 total subjects will
be randomly assigned to minocycline or control (1:1). The first dose will be given
intravenously. Subsequent doses will be given orally every 24 hours for a total of five
doses. The study will test to see if the medication is safe in intracerebral hemorrhage. The
pharmacokinetics of minocycline in intracerebral hemorrhage will be determined and the impact
of minocycline on blood biomarkers.

Inclusion Criteria:

- 18 years of age or older.

- Intracerebral hemorrhage documented by CT scan

- The first dose of the drug can be administered within 12 hours of time last known to
be at baseline

Exclusion Criteria:

- Allergy to tetracycline antibiotics

- Pregnancy or suspected pregnancy (pregnancy test will be done on women of
child-bearing potential)

- Hepatic and/or renal insufficiency (LFT's >3x upper limit of normal; Creatinine
>2mg/dL)

- History of intolerance to minocycline

- National Institutes of Health Stroke Scale score of 4 or less

- Glasgow Coma Scale score of 5 or less

- Surgical evacuation of hematoma planned within 24 hours

- Secondary intracerebral hemorrhage resulting from trauma, arteriovenous malformation,
aneurysm, tumor or other causes

- Thrombocytopenia (platelet count <75,000/mm3) or coagulopathy (INR >1.4)

- Previously not independent (prestroke modified Rankin scale score >2)

- Suspected of not being able to comply with the study protocol

- Unlikely to be available for 90 day follow-up

- Pre-existing Do Not Resuscitate (DNR) order or indication that a new DNR order will be
implemented within the first 48 hours of hospitalization