Phase 2
N=76
Phase 2a Dose-Ranging Study to Evaluate Safety and Effectiveness of AA4500 in Treatment of Dupuytren's Disease Nodules
Dupuytren's Disease
Bottom Line
View on ClinicalTrials.gov: NCT02193828 ↗Enrolled (actual)
76
Serious AEs
0.0%
Results posted
Jul 2015
Primary outcome: Primary: Percent Change From Baseline in Surface Area and Volume of the Treated Nodule at Day 57 Using Caliper Measurements — -81.61; -80.11; -58.30; -41.76 percentage of change — p=<.0001
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 2
- Interventions
- Collagenase clostridium histolyticum (Biological); Placebo (Biological)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Endo Pharmaceuticals
- Primary completion
- Dec 2014
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Percent Change From Baseline in Surface Area and Volume of the Treated Nodule at Day 57 Using Caliper Measurements |
-81.61; -80.11; -58.30; -41.76; -89.03; -87.58 | <.0001 sig |
| SECONDARY Percent Change From Baseline in Surface Area and Volume of the Treated Nodule at Day 57 Using Ultrasound |
-34.23; -19.37; -10.30; -4.54; -40.99; -13.01 | .2431 |
| SECONDARY Change From Baseline in Consistency of the Treated Nodules at Day 57 |
-1.9; -1.9; -1.2; -0.3 | .0002 sig |
| SECONDARY Percent Change From Baseline in Hardness of the Treated Nodule at Day 57 |
-17.05; -30.40; -17.87; 4.80 | .0004 sig |
| SECONDARY Change From Baseline in Nodular Pain of the Treated Nodule at Day 57 |
-0.8; -1.6; -1.7; -0.5 | .3135 |
| SECONDARY Investigator Global Assessment of Improvement With Treatment |
1.7; 1.7; 2.5; 3.0 | .0006 sig |
| SECONDARY Subject Satisfaction With Treatment |
1.5; 1.6; 2.3; 2.8 | .0048 sig |
| SECONDARY Composite Responder Analysis |
14; 16; 12; 6; 4; 2 | .0065 sig |
Summary
The objectives of this study are to assess the safety and effectiveness of AA4500 in treating palmar Dupuytren's disease nodules.
Eligibility Criteria
Inclusion Criteria
- 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
Exclusion Criteria
- 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
Data sourced from ClinicalTrials.gov (NCT02193828). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.