An Efficacy and Safety Study of Palovarotene to Treat Preosseous Flare-ups in FOP Subjects

Completed · Phase 2 · Has a placebo group

Conditions studied: Fibrodysplasia Ossificans Progressiva

In brief

Fibrodysplasia ossificans progressiva (FOP) is a rare, severely disabling disease characterized by painful, recurrent episodes of soft tissue swelling (flare-ups) that result in abnormal bone formation in muscles, tendons, and ligaments. Flare-ups begin early in life and may occur spontaneously or after soft tissue trauma, vaccinations, or influenza infections. Recurrent flare-ups progressively restrict movement by locking joints leading to cumulative loss of function and disability. Mouse models of FOP have demonstrated the ability of retinoic acid receptor (RAR) gamma agonists to prevent heterotopic ossification (HO) following injury. The purpose of the study is to evaluate whether palovarotene, an RAR gamma agonist, will prevent HO during and following a flare-up in subjects with FOP.

Key facts

Study ID

NCT02190747

Run by

Clementia Pharmaceuticals Inc.

People needed

40

Starts

2014-07-14

Expected to finish

2016-05-23

Last updated by the study team

2021-02-16

Who can join

Age: 6 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Written, signed, and dated informed subject/parent consent or age-appropriate assent.
• Subjects clinically diagnosed with classic Fibrodysplasia Ossificans Progressiva (FOP).
• Symptomatic onset of a distinct flare-up within 7 days of Study Day 1 (start of study drug) and defined by the presence of at least two of six of the following symptoms: pain, soft tissue swelling, decreased range of motion, stiffness, redness, and warmth. Flare-up must be confirmed by the physician at the Screening visit.
• Flare-up is at an appendicular area (upper or lower extremity), abdomen, or chest; and subject has received, is receiving, or is willing to receive treatment per standard of care, which may or may not include oral prednisone (2 mg/kg PO to a maximum dose of 100 mg daily) for 4 days.
• Abstinent or using two highly effective forms of birth control.
• Subjects must be accessible for treatment and follow-up. Subjects living at distant locations from the investigational site must be able and willing to travel to a site for the initial and all follow-up visits.

You may not qualify if…

• Weight <20 kg.
• Intercurrent non-healed fracture at any location.
• Complete immobilization of joint at site of flare-up.
• The inability of the subject to undergo imaging assessments using plain radiographs.
• If currently using vitamin A or beta carotene, multivitamins containing vitamin A or beta carotene, or herbal preparations, fish oil, and unable or unwilling to discontinue use of these products for the duration of the study.
• Exposure to synthetic oral retinoids in the past 30 days prior to Screening (signature of the informed consent).
• Concurrent treatment with tetracycline due to the potential increased risk of pseudotumor cerebri.
• History of allergy or hypersensitivity to retinoids or lactose.
• Concomitant medications that are inhibitors or inducers of CYP450 3A4 activity.
• Amylase or lipase >1.5x above the upper limit of normal or with a history of chronic pancreatitis.
• Elevated aspartate aminotransferase or alanine aminotransferase >2.5x the upper limit of normal.
• Fasting triglycerides >400 mg/dL with or without therapy.

Where it is running

• University of California San Francisco, Division of Endocrinology and Metabolism — San Francisco, California, United States
• University of Pennsylvania, Center for Research in FOP & Related Disorders — Philadelphia, Pennsylvania, United States
• Hôpital Necker-Enfants Malades, Department of Genetics — Paris, France
• The Royal National Orthopaedic Hospital, Brockley Hill — Stanmore, Middlesex, United Kingdom

Full record on ClinicalTrials.gov

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