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Completed

NCT Number: NCT01171859

Safety, Efficacy and Pharmacokinetics of Doxycycline Plus Tauroursodeoxycholic Acid in Transthyretin Amyloidosis

This study is being conducted to explore the potential benefits of a twelve-month doxycycline (at the best tolerated dose of 200 mg/day) and tauroursodeoxycholic acid (750 mg/day) treatment on disease progression in patients affected by transthyretin amyloidosis, including: 1) patients not eligible for liver transplantation; 2) patients eligible for liver transplantation, as a "bridge" therapy between the time of diagnosis and surgery, with the aim of stabilizing the disease; 3) patients showing disease progression after liver transplantation performed since at least 1 year.

It is a phase II, therapeutic exploratory, two-part, 18-month, single centre, prospective study.

Part I is a 12-month, open label treatment period in which doxycycline (200 mg/day, continuously) and tauroursodeoxycholic acid (750 mg/day continuously) are administered to 40 consenting subjects with transthyretin amyloidosis. Part II is a withdrawal period in which subjects will be monitored for disease progression. During part I, subjects will be evaluated at baseline (study Day 0), and then after 3, 6, 9 and 12 months of doxycycline plus tauroursodeoxycholic acid treatment or at premature treatment discontinuation; during part II, they will be assessed at months 15 and 18. Monthly phone contacts and blood tests will be performed to monitor potential adverse events.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Amyloid Research and Treatment Centre, Biotechnology Research Laboratories

Pavia, 27100, Italy

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Histochemical diagnosis of amyloidosis as based on detection by polarizing microscopy of green birefringent material in Congo red-stained tissue specimens;
  • Molecular definition of the transthyretin (TTR) mutation or immunohistochemical staining of amyloid fibrils with anti-TTR antibody;
  • ECOG performance status (PS) 0, 1, 2;
  • New York Heart Association (NYHA) class ≤III
  • Systolic blood pressure ≥100 mmHg (standing)
  • Must have symptomatic organ involvement with amyloid to justify therapy; must have evidence of neuropathy and/or cardiomyopathy progression after liver transplantation performed since at least one year.
  • Contraception for women of childbearing potential. Medically approved contraception could include abstinence. A negative serum pregnancy test is required prior to initiation of treatment with study medication.

Exclusion criteria

  • Liver transplantation in the previous 12 months or liver transplantation anticipated in less than 6 months;
  • ALT and/or AST ≥ 2 x Upper Normal Limit (UNL);
  • Alkaline phosphatase ≥ 2 x UNL;
  • Creatinine clearance < 30 ml/min;
  • Any other lab values that in the opinion of the investigator might place the subject at unacceptable risk for participation in the study;
  • Echocardiographic ejection fraction < 50%;
  • Other neuropathies, due to vitamin B12 deficiency, alcoholism, hypothyroidism, uremia, diabetes mellitus, vasculitides;
  • History of poor compliance;
  • History of hypersensitivity to any of the ingredients of the study therapies;
  • Use of any investigational drug, device (or biologic) within 4 weeks prior to study entry or during the study.

Treatment and study plan

Doxycycline + Tauroursodeoxycholic acid

Drug

doxycycline 100 mg twice a day for 12 months; tauroursodeoxycholic acid 250 mg three times a day for 12 months

Primary outcomes

  1. Response rate to doxycycline + tauroursodeoxycholic acid treatment

    Time frame: One year

    A responder is a subject with:

    • a modified body mass index (mBMI) reduction of less than 10% and a change in the Neurologic Impairment Score-Lower Limbs (NIS-LL) <2 (in subjects with peripheral neuropathy);
    • a modified body mass index (mBMI) reduction of less than 10% and an increase in N-terminal natriuretic peptide type B (NT-proBNP) concentration of less than 30% or < 300 pg/mL (in subjects with isolated cardiomyopathy).

Secondary outcomes

  1. Number of patients experiencing treatment-emergent adverse events

    Time frame: One year

  2. Change in quality of life

    Time frame: Every six months

    SF-36 scale

  3. doxycycline pharmacokinetics (PK)

    Time frame: Every three months

  4. response in autonomic dysfunction, sensory-motor peripheral neuropathy and visceral organ involvement

    Time frame: One year

    response assessed according to the Kumamoto Scale score

  5. neurologic response

    Time frame: One year

    response assessed by motor and sensory nerves conduction studies

  6. Incidence of patients discontinuing from the study because of clinical or laboratory adverse events

    Time frame: One year

Sponsors and collaborators

Lead sponsor

Fondazione IRCCS Policlinico San Matteo di Pavia

Other

Registry information

Official study title

A Single Center, Twelve-month, Open-label, Prospective Study Followed by a Six-month Withdrawal Period to Evaluate the Efficacy, Tolerability, Safety and Pharmacokinetics of Doxycycline in Combination With Tauroursodeoxycholic Acid in Transthyretin Amyloidosis

Important dates

Study start
2010
Primary completion
2015
Study completion
2015
First posted
Jul 29, 2010
Registry last updated
Feb 25, 2016

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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