Phase 2a Dose-Ranging Study to Evaluate Safety and Effectiveness of AA4500 in Treatment of Dupuytren's Disease Nodules
Completed · Phase 2 · Has a placebo group
Conditions studied: Dupuytren's Disease
In brief
The objectives of this study are to assess the safety and effectiveness of AA4500 in treating palmar Dupuytren's disease nodules.
Key facts
- Study ID
- NCT02193828
- Run by
- Endo USA Inc., a Keenova Therapeutics Company
- People needed
- 76
- Starts
- 2014-07-01
- Expected to finish
- 2014-12-01
- Last updated by the study team
- 2017-10-05
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Provide a signed and dated informed consent
- Be a man or woman ≥ 18 years of age
- Have a diagnosis of Dupuytren's disease AND have at least one palmar nodule on the selected hand that is:
- Palpable
- Measures between 0.5 cm and 2.0 cm in length and between 0.5 cm and 2.0 cm in width using hand-held calipers n
- Not directly associated with a Dupuytren's cord
- Have a negative urine pregnancy test at screening and before injection of study drug and be using a highly effective (ie, < 1% failure rate) contraception method as judged by the investigator (eg, abstinence, intrauterine device [IUD], hormonal [estrogen/progestin] contraceptives, or barrier control) for at least one menstrual cycle prior to study enrollment and for the duration of the study or be surgically sterile (if female of childbearing potential); or be a postmenopausal female (no menses for at least 1 year or hysterectomy)
- Be able to comply with the study visit schedule as specified in the protocol
You may not qualify if…
- Received steroid injections (eg, tri-amcinolone acetonide) on the selected nodule within 3 months before administration of study drug
- Has a chronic muscular, neurological, or neuromuscular disorder that affects the hands
- Has a known systemic allergy to collagenase or any other excipient of AA4500
- Has received any collagenase treatments (eg, Santyl® ointment and/or XIAFLEX®/XIAPEX®) within 30 days before injection of study drug in the hand selected for treatment
- Is currently receiving or plans to receive anticoagulant medication or has received anticoagulant medication (except for ≤ 150 mg aspirin daily) within 7 days before injection of study drug
- Has a known recent history of stroke, bleeding, or other medical condition, which in the investigator's opinion would make the subject unsuitable for enrollment in the study
- Received an investigational drug within 30 days before injection of study drug
- Is pregnant or intends on becoming pregnant during the study or is breastfeeding a child
- Has any clinically significant medical history or condition(s), including conditions that affect the hands, that would, in the opinion of the investigator, substantially increase the risk associated with the subject's participation in the protocol or compromise the scientific objectives of the study
- Had surgery on the selected hand within 3 months before the screening visit
- Has jewelry on the hand to be treated that cannot be removed
Where it is running
- Tucson Orthopaedic Institute — Tucson, Arizona, United States
- CORE Orthopaedic Medical Center — Encinitas, California, United States
- Marin Endocrine Care & Research, Inc. — Greenbrae, California, United States
- Brigid Freyne, MD, Inc. — Murrieta, California, United States
- Indiana Hand to Shoulder Center — Indianapolis, Indiana, United States
- State University of New York — Stony Brook, New York, United States
- OrthoCarolina Research Institute, Inc. — Charlotte, North Carolina, United States
- Orthopedic and Reconstructive Center — Oklahoma City, Oklahoma, United States
- Blair Orthopedic Associates, Inc. — Altoona, Pennsylvania, United States
- Brisbane Hand & Upper Limb Clinic — Brisbane, Queensland, Australia
- Houston Medical — Kippa-Ring, Queensland, Australia
Full record on ClinicalTrials.gov
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