Status and phase
Conditions
Treatments
About
The Primary objective of this study is to evaluate the efficacy of VX-150 in the treatment of osteoarthritis pain
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
Exclusion criteria
History in the past 10 years of reactive arthritis, rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, arthritis associated with inflammatory bowel disease, sarcoidosis, amyloidosis or fibromyalgia.
History in the past 10 years of malignancy with the exception of resected basal cell carcinoma, squamous cell carcinoma of the skin or resected cervical atypia or carcinoma in situ.
History of cardiac dysrhythmias requiring anti-arrythmia treatment(s).
History of abnormal laboratory results ≥2.5 × upper limit of normal (ULN) indicative of any significant medical disease which in the opinion of the investigator would preclude the subjects participation in the study.
A known or clinically suspected infection with human immunodeficiency virus or hepatitis B or C viruses.
Other serious, acute or chronic medical or psychiatric illness that in the judgment of the investigator could compromise subject safety, limit the subject's ability to complete the study and/or compromise the objectives of the study.
Either participated within 3 months in another investigational study in which the subject was exposed to study drugs or vaccines,or will participate concurrently in such study.
History of drug or alcohol dependence in the past 3 years, or a positive test for drugs of abuse at the Screening Visit.
Requires opioids for pain relief.
Changed analgesic treatment regimen within 30 days of the Screening Visit.
Received or plan to receive short acting hyaluronic acid, corticosteroid, or other intra-articular injections as follows:
Received or plan to receive long acting hyaluronic acid or other intra-articular injections as follows:
History of arthroscopic or open surgery within 12 months before the Screening Visit, or have a planned surgery during, or immediately after, study follow-up.
History of joint replacement surgery in the index knee.
Significant hip pain, ipsilateral to the index knee that may interfere with assessments of index knee pain.
Clinical signs and symptoms of an active knee infection.
Current use of a handicap assistance device (unilateral assistance device such as a cane is permitted).
Started a new physical therapy, weight loss, or exercise program within 3 months of the Screening Visit, or are not willing to maintain a stable program during the course of the study.
Lab abnormalities at the screening visit.
Primary purpose
Allocation
Interventional model
Masking
124 participants in 2 patient groups
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Data sourced from clinicaltrials.gov
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