Dupuytren's Contracture Clinical Trial
Official title:
A Phase 1, Open-Label Study to Assess the Pharmacokinetics and Safety of a Single Injection of AA4500 0.58 mg in Subjects With Dupuytren's Contracture
A Phase 1, open-label, single-dose pharmacokinetic study in subjects with Dupuytren's
contracture conducted at one site in the United States. All subjects received a single dose
of AA4500 0.58 mg, which was injected directly into the cord affecting either the
metacarpophalangeal (MP) or proximal interphalangeal (PIP) joint. Pharmacokinetic blood
samples were collected before dosing, at predetermined time points through the 24 hours after
dosing, Day 7, and Day 30. Efficacy and safety assessments were performed up to 30 days after
the AA4500 0.58 injection.
This study was designed to be part of the larger clinical program, for adult patients with
Dupuytren's contracture with a palpable cord, where the data from 2 pivotal
Placebo-Controlled studies (AUX-CC-857 [NCT00528606]and AUX-CC-859 [NCT00533273]) and 7
non-pivotal studies were evaluated.
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Status | Clinical Trial | Phase | |
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