Doxycycline
Drug200 mg/day (100 mg twice daily, orally) for 4 weeks with a pause of 2 weeks in combination with UDCA
Other names: Doxyferm
NCT Number: NCT02016365
The primary objective for this study is to evaluate the efficacy of doxycycline + ursodeoxycholic acid (UDCA) on disease progression in Transthyretin Amyloidosis (ATTR) subjects with cardiomyopathy with or without neuropathy.
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Notify Me50 year and older
All sexes
Interventional
Phase 2
Dept of Clinical Medicin, Ptieå Hospital, Piteå, Sweden
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
200 mg/day (100 mg twice daily, orally) for 4 weeks with a pause of 2 weeks in combination with UDCA
Other names: Doxyferm
750 mg/day (500 mg +250mg orally) continuously
Other names: Ursofalk
Time frame: At 12 month treatment
The primary endpoint of the study is the response rate to doxycycline + UDCA treatment at month 12. A responder is an ATTR subject with:
Time frame: 12 month
mBMI-reduction of less than 10%
Time frame: 12 month
Increase of septum thickness ≤ 2 mm
Time frame: 6, 12 and 18 month
To assess the change from baseline in the neurologic Kumamoto Scale
Time frame: During 12 month treatment and during 6 month follow-up
To assess the tolerability and safety of the treatment, the number of patients with adverse reactions will be recorded.
Monthly phone contacts will be performed for monitoring of the treatment safety.
The safety profile of doxycycline + UDCA will be assessed through the recording, reporting and analysis of baseline medical conditions, physical examination findings including vital signs and laboratory tests. These will be compared to analysis results observed during the study.
Time frame: 18 months
To assess the tolerability and safety of the treatment, blood work [e.g.complete blood count, creatinine and aspartate transaminase (AST), alkaline phosphatase(ALT)] for potential drug-related adverse events will be drawn at 1, 3, 6, 9, 12 and 18 month.
The safety profile of doxycycline + UDCA will be assessed through the recording, reporting and analysis of baseline medical conditions, physical examination findings including vital signs and laboratory tests. These will be compared to analysis results observed during the study.
Umeå University
Other
A Phase II Multicenter Pilot Study of the Safety and Efficacy of Doxycycline/UrsoDeoxyCholicAcid on Disease Progression in ATTR Amyloidosis
Acronym: Dox/Urso
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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