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Spots Global Cancer Trial Database for AA4500 (XIAFLEX™, Proposed Name) in the Treatment of Dupuytren's Contracture

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Trial Identification

Brief Title: AA4500 (XIAFLEX™, Proposed Name) in the Treatment of Dupuytren's Contracture

Official Title: A Phase 3, Double-Blind, Randomized, Placebo-Controlled Study of the Safety and Efficacy of AA4500 in the Treatment of Subjects With Dupuytren's Contracture

Study ID: NCT00528606

Study Description

Brief Summary: This was a Phase 3, double-blind, randomized, placebo-controlled study conducted in the United States. Subjects with a diagnosis of Dupuytren's contracture in a metacarpophalangeal (MP) or proximal interphalangeal (PIP) joint that resulted in a fixed flexion deformity of at least one finger, other than the thumb, that was at least 20° as measured by finger goniometry and was suitable for injection were randomized 2:1 to receive AA4500 0.58 mg or placebo. 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.

Detailed Description:

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

100 UCLA Medical Plaza, Suite 305, Los Angeles, California, United States

Hand Surgery Clinic, Palo Alto, California, United States

Hand Surgery Associates, PC, Denver, Colorado, United States

The Hand and Upper Extremity Center of Georgia, P.C., Atlanta, Georgia, United States

Rockford Orthopedic Associates, Ltd., Rockford, Illinois, United States

The Indiana Hand Center, Indianapolis, Indiana, United States

Brigham and Women's Hospital, Department of Orthopedic Surgery, Boston, Massachusetts, United States

Newton-Wellesley Hospital, Newton, Massachusetts, United States

TRIA Orthopaedic Center, Minneapolis, Minnesota, United States

Hospital for Special Surgery, New York, New York, United States

SUNY Stony Brook - Department of Orthopedics, Stony Brook, New York, United States

Health Research Institute, Oklahoma City, Oklahoma, United States

Hand Microsurgery & Reconstructive Orthopaedics, Erie, Pennsylvania, United States

University Orthopedics Center, State College, Pennsylvania, United States

Department of Orthopaedics, Brown University, Rhode Island Hospital, Providence, Rhode Island, United States

Contact Details

Name: Veronica Urdaneta, MD

Affiliation: Endo Pharmaceuticals

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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