Doxycycline to Upgrade Organ Response in Light Chain (AL) Amyloidosis Trial

• Status: Completed
• Trial end date: 2020-05-19
• Target enrollment: 0
• Participant gender: All

Summary

In this study the investigators want to find out more about the addition of the antibiotic, doxycycline, to standard anti-amyloid therapy in people with amyloidosis. The investigators want to find out whether doxycycline improves the response to standard anti-amyloid therapy and whether it causes any problems (side effects).

• Phase: Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Medical College of Wisconsin
• Collaborator: National Heart, Lung, and Blood Institute (NHLBI)
• Treatments: Doxycycline

Criteria

Inclusion Criteria:

1. Patients with biopsy proven AL amyloidosis.

2. Patients ≥ 18 years of age are eligible.

3. Patient must provide informed consent.

4. All patients must have measurable amyloid organ involvement of a vital organ (eg. heart, liver, kidneys). Localized amyloidosis will also be eligible as long as the amyloid involvement is radiologically measurable.

5. A negative pregnancy test will be required for all women of child bearing potential. Breast feeding is not permitted.

6. Patients who have previously been taking doxycycline will be eligible as long as there is no contraindication to stay on doxycycline 100 mg twice daily (BID) for 1 year in the opinion of the treating physician.

7. Creatinine clearance of >25 ml/min.

Exclusion Criteria:

1. Patients with severe malabsorption syndrome precluding absorption of oral agents will be excluded.

2. Known intolerance or allergic reactions with doxycycline.

3. Previous chemotherapy for AL amyloidosis.