ClinicalTrials.Veeva

Menu

Antibiotics Against Amyloid Angiopathy (BATMAN)

L

Leiden University Medical Center (LUMC)

Status and phase

Enrolling
Phase 2
Phase 1

Conditions

Cerebral Amyloid Angiopathy

Treatments

Drug: Placebo
Drug: Minocycline

Study type

Interventional

Funder types

Other

Identifiers

NCT05680389
2019-004786-41 (EudraCT Number)
P19.110

Details and patient eligibility

About

We will perform a randomized clinical trial with minocycline. Minocycline is an antibiotic of the tetracycline family and known to modulate inflammation, gelatinase activity and angiogenesis, which we know are central mechanisms in CAA-pathology. Our aim is to prove in a randomized clinical trial in a translational setting that minocycline treatment (duration 3 months) can decrease markers of neuroinflammation and the gelatinase pathway in the cerebrospinal fluid (CSF) of persons with D-CAA (n=30) and sporadic-CAA (n=30).

Enrollment

60 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age ≥18 years for D-CAA and age ≥55 years for sporadic-CAA
  • Probable-CAA according to the Modified-Boston-Criteria or genetically proven D-CAA
  • ≤ 2 ICH (occurrence of ICHs at least 1 year ago) and presence of ≥ 2 lobar microbleeds +/-cortical superficial siderosis
  • Written informed consent

Exclusion criteria

  • Previous allergic reactions to minocycline
  • Modified Rankin Score ≥3
  • Contraindications, such as:
  • Contraindications for 7T MRI as determined by the 7Tesla safety committee. Examples of possible contra-indications are: claustrophobia, pacemakers and defibrillators, nerve stimulators, intracranial clips, intraorbital or intraocular metallic fragments, cochlear implants, ferromagnetic implants, hydrocephalus pump, intra-uterine device, permanent make-up, tattoos above the shoulders. In case of specific contra-indications for 7T a 3T will be made instead. - Specific contraindications for checkerboard fMRI: seizure within prior year, photosensitive epilepsy, noncorrectable visual impairment. - Contraindications for lumbar puncture: compression of the spinal cord, signs and symptoms of increased intracranial pressure, local infections of the skin at the puncture site, a coagulopathy or thrombocytopenia (<100). (Use of acetylsalicylic acid, NSAIDs, COX2 inhibitors or low-molecular-weight heparin are no contraindications for lumbar puncture.)
  • Pregnancy/breast feeding
  • Liver/renal failure
  • Use of antibiotics <1 month
  • SLE or other diseases known to generate inflammatory responses
  • Previous/current/planned use of retinoids (since this is related to increasing risk of increased intracranial pressure)
  • Current use of anaesthetics like methoxyflurane, agents inhibiting peristalsis, barbiturates, carbamazepine or fenytoïne

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

60 participants in 2 patient groups, including a placebo group

Minocycline
Experimental group
Description:
100 mg twice daily for 3 months
Treatment:
Drug: Minocycline
Placebo
Placebo Comparator group
Description:
twice daily for 3 months
Treatment:
Drug: Placebo

Trial contacts and locations

1

Loading...

Central trial contact

Sabine Voigt, BSc; Marieke Wermer, PhD

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems