CTX
Cross-source consensus on CTX from 1 sources and 4 claims.
1 sources · 4 claims
Uses
Risks & contraindications
Interactions
Evidence quality
Highlighted claims
- The MOI-A primary endpoint is the percentage change in serum CTX from baseline to week 24. — Matrix-directed therapy losartan to identify the effect on the bone resorption marker carboxy-terminal crosslink of type I collagen telopeptide (CTX) in older adolescents and adults with osteogenesis imperfecta recruited from secondary care sites: the ‘MOI-A’ study; a randomised, phase 2/pilot, dose
- Recent fractures are excluded because they can elevate CTX for up to 6 months before enrolment. — Matrix-directed therapy losartan to identify the effect on the bone resorption marker carboxy-terminal crosslink of type I collagen telopeptide (CTX) in older adolescents and adults with osteogenesis imperfecta recruited from secondary care sites: the ‘MOI-A’ study; a randomised, phase 2/pilot, dose
- The efficacy threshold for defining the Optimal Biologic Dose is at least a 30% reduction in CTX. — Matrix-directed therapy losartan to identify the effect on the bone resorption marker carboxy-terminal crosslink of type I collagen telopeptide (CTX) in older adolescents and adults with osteogenesis imperfecta recruited from secondary care sites: the ‘MOI-A’ study; a randomised, phase 2/pilot, dose
- Prior bisphosphonate and denosumab treatment could confound CTX because they reduce bone resorption. — Matrix-directed therapy losartan to identify the effect on the bone resorption marker carboxy-terminal crosslink of type I collagen telopeptide (CTX) in older adolescents and adults with osteogenesis imperfecta recruited from secondary care sites: the ‘MOI-A’ study; a randomised, phase 2/pilot, dose