Terminated/Withdrawn
Sponsor ID
20080733

AMG 745 in Subjects with Age-associated Muscle Loss

Sponsor ID
20080733
Clinicaltrials.gov ID
NCT00975104
EUCTIS ID
N/A
EudraCT ID
N/A

Study Details

Randomized, Double-blind, Placebo-controlled Dose Ranging Study to Evaluate the Safety and Efficacy of AMG 745 in Age-associated Muscle Loss

Additional Study Details

Phase
Phase 2
Product
AMG 745
Type
Interventional
Masking
Double (Participant, Investigator)
Enrollment
200
Additional Study Details

Protocol Summary

Primary Outcome Measures

To evaluate the effect of AMG 745 weekly IV doses of 0.3 mg/kg, 1.0 mg/kg, or 3.0 mg/kg, compared with weekly IV placebo on thigh muscle CSA in subjects ≥ 65 yrs old with limited exercise tolerance and functional limitations

Timeframe: 12 Weeks

Secondary Outcome Measures

To evaluate the effect of treatment with AMG 745 on muscle strength (hand grip strength) and function (gait speed, 10-step stair climb power, chair stand and 6 minute walk distance) and to evaluate the PK of AMG 745 following multiple IV administrations

Timeframe: 12 Weeks

Locations

No locations found.