LivingGLP1
Long acting GLP-1 receptor agonist (injectable)

Albiglutide 50 mg subcutaneous once weekly

ALBI_SC_50MG_QW

Agent
albiglutide
Route
SC
Dose
50 mg
Frequency
QW
Dosing
fixed
Mechanism
GLP-1 receptor agonist; daily or weekly (liraglutide; dulaglutide; semaglutide; exenatide extended release; albiglutide; efpeglenatide; loxenatide; taspoglutide and others)
Trials
3
Participants in these arms
504

Withdrawn from the market in 2018 for commercial reasons.

Effects across outcomes

Bayesian random effects estimate against the comparator of each analysis (usually placebo), posterior median and 95% credible interval. Green: clearly better; red: clearly worse.
ConditionOutcomeWindowVersusEffect (95% CrI)SUCRA
Type 2 diabetes (adults)HbA1c changeweeks 20 to 36 (target week 26)PlaceboMD -1.47 (-2.00 to -0.63)0.70
Type 2 diabetes (adults)HbA1c changeweeks 36 to 64 (target week 52)PlaceboMD -1.35 (-2.30 to 0.39)0.70
Type 2 diabetes (adults)HbA1c changeweeks 36 to 64 (target week 52)PlaceboMD -1.01 (-1.93 to 0.09)0.36
Type 2 diabetes (adults)Body weight change in kilograms (diabetes)weeks 20 to 36 (target week 26)PlaceboMD 0.85 (-2.91 to 5.34)0.31
Type 2 diabetes (adults)Body weight change in kilograms (diabetes)weeks 36 to 64 (target week 52)PlaceboMD 1.72 (-3.88 to 7.36)0.32
Type 2 diabetes (adults)Body weight change in kilograms (diabetes)weeks 36 to 64 (target week 52)PlaceboMD -0.19 (-5.33 to 4.61)0.20
Type 2 diabetes (adults)HbA1c below 7 percentweeks 20 to 36 (target week 26)PlaceboOR 14.70 (3.10 to 57.09)0.79
Type 2 diabetes (adults)HbA1c below 7 percentweeks 36 to 64 (target week 52)PlaceboOR 2.31 (0.57 to 7.42)0.31
Type 2 diabetes (adults)HbA1c below 7 percentweeks 36 to 64 (target week 52)PlaceboOR 4.00 (0.49 to 17.14)0.49
Type 2 diabetes (adults)Level 2 or 3 hypoglycemia (participants)longest follow-upPlaceboHR 0.50 (0.04 to 4.76)0.46
Type 2 diabetes (adults)Level 2 or 3 hypoglycemia (participants)longest follow-upPlaceboHR 5.45 (2.00 to 15.27)0.22
Type 2 diabetes (adults)Level 2 or 3 hypoglycemia (participants)longest follow-upPlaceboHR 1.61 (0.74 to 3.41)0.44
Type 2 diabetes (adults)Level 2 or 3 hypoglycemia (participants)longest follow-upPlaceboHR 1.23 (0.27 to 5.00)0.43
Type 2 diabetes (adults)Serious adverse eventslongest follow-upPlaceboHR 1.21 (0.74 to 1.94)0.38
Type 2 diabetes (adults)Discontinuation due to adverse eventslongest follow-upPlaceboHR 1.84 (0.64 to 5.66)0.45
Type 2 diabetes (adults)Nausealongest follow-upPlaceboHR 1.50 (0.80 to 2.76)0.69
Type 2 diabetes (adults)Vomitinglongest follow-upPlaceboHR 2.57 (0.54 to 11.23)0.50
Type 2 diabetes (adults)Diarrhealongest follow-upPlaceboHR 1.15 (0.69 to 1.91)0.65
Type 2 diabetes (adults)Constipationlongest follow-upPlaceboHR 2.38 (1.07 to 5.53)0.35
Type 2 diabetes (adults)Acute pancreatitislongest follow-upPlaceboHR 1.09 (0.09 to 12.19)0.42

Trials