| Bupropion versus placebo | |||
| Anderson, 2002 | bupropion SR 300, or 400 mg/d. versus placebo | obese adults | double-blind Follow-up duration: 24 weeks |
| Croft, 2002 | Bupropion, 300 mg for 44 wk versus Placebo | patients with major depression responder to open-label treatment with bupropion SR | double-blind Follow-up duration: 44 weeks |
| Jain, 2002 | bupropion SR 300 mg/d versus Placebo | Obese adults (body mass index, 30 to 44 kg/m(2)) not currently meeting criteria for major depression but with depressive symptoms (Beck Depression Inventory score 10-30) | double-blind Follow-up duration: 26 weeks |
| Fluoxetine versus placebo | |||
| Breum, 1995 | Fluoxetine, 60 mgfor 52 wk versus Placebo | aaaa | |
| Connolly, 1995 | fluoxetine 60 mg daily versus placebo | obese elderly patients over 60 years of age with Type 2 diabetes | double-blind |
| Darga, 1991 | fluoxetine versus placebo | obese subjects | Follow-up duration: 52 weeks |
| Goldstein, 1994 | Fluoxetine, 60 mgfor 52 wk versus Placebo | obese outpatients | double-blind Follow-up duration: 52-week |
| Gray, 1992 | Fluoxetine, 60 mg for 6 mo versus Placebo | obese, type 2 non-insulin dependent diabetics being treated with insulin | double blind Follow-up duration: 24 weeks |
| Marcus, 1990 | Fluoxetine, 60 mgfor 52 wk versus Placebo | ||
| Mendoza Espejo, 1995 | Fluoxetine, 180 mgfor 6 mo versus Placebo | ||
| Michelson 50wk, 1999 | Fluoxetine, 20 mgfor 50 wk versus Placebo | ||
| O’Kane, 1994 | versus | ||
| liraglutide versus placebo | |||
| Astrup (NN8022-1807 ), 2009 NCT00422058 | 4 liraglutide doses (1.2 mg, 1.8 mg, 2.4 mg, or 3.0 mg daily) versus placebo | obese individuals without type 2 diabetes | double blind Follow-up duration: 20 weeks Europe |
| lorcaserin versus placebo | |||
| APD356-004, 2009 | versus | ||
| BLOOM, 2010 NCT00395135 | lorcaserin 10mg bid versus placebo | double-blind Follow-up duration: 52 weeks | |
| BLOOM-DM (10mg bid), NCT00603291 | lorcaserin 10 mg BID versus placebo | overweight and obese patients with type 2 diabetes mellitus managed with oral hypoglycemic agents | double-blind Follow-up duration: 52 weeks |
| BLOSSOM (10mg bid), 2009 NCT00603902 | lorcaserin 10 mg twice daily versus placebo | obese and overweight patients | double blind Follow-up duration: 1 year USA |
| Orlistat versus placebo | |||
| Bakris, 2002 | orlistat versus placebo | obese individuals with inadequately controlled hypertension. | double-blind Follow-up duration: 1-year |
| Broom, 2002 | orlistat versus placebo | obese patients with cardiovascular risk | double-blind Follow-up duration: 54-week |
| Broom,, 2001 | versus | ||
| Davidson, 1999 | orlistat, 120 mg 3 times a day, for 52 weeks versus placebo | Obese adults (BMI 30-43 kg/m2) | double-blind Follow-up duration: 52 weeks US |
| Deerochanawong,, 2001 | versus | ||
| Derosa, 2003 | orlistat 120 mg TID versus placebo | obese patients with hypercholesterolemia | double-blind Follow-up duration: 1-year |
| Gotfredsen, 2001 | versus | ||
| Halpern, 2003 | orlistat (120 mg t.i.d.), versus placebo | Obese, non-insulin-dependent diabetic patients, aged 18-70 years old, with BMI > 27 kg/m2 | Double-blind Follow-up duration: 24 weeks Latin-America |
| Hanefeld, 2002 | orlistat 120 mg t.i.d. versus placebo | Overweight or obese adults (BMI >or= 28 kg/m2) with HbA1c of 6.5-11% and clinical type 2 diabetes | double-blind Follow-up duration: 48-week |
| Hauptman, 2000 | 60 mg of orlistat TID or 120 mg of orlistat TID, versus placebo | obese patients (BMI 30-44 kg/m2) | double-blind Follow-up duration: 1 year USA |
| Hill, 1999 | 30 mg orlistat, 60 mg orlistat, or 120 mg orlistat 3 times daily for 1 y versus placebo | Obese subjects who lost > or = 8% of their initial body weight during a 6-mo lead-in of a prescribed hypoenergetic diet (4180-kJ/d deficit) with no adjunctive pharmacotherapy | double-blind Follow-up duration: 1 year |
| Hollander, 1998 | 120 mg orlistat orally three times a day versus placebo | obese men and women with type 2 diabetes who were aged > 18 years, had a BMI of 28-40 kg/m2, and were clinically stable on oral sulfonylureas | double-blind Follow-up duration: 57-week |
| Karhunen, 2000 | orlistat 120 mg t.i.d.
versus placebo | obese subjects | double-blind Follow-up duration: 1 y. |
| Kelley, 2002 | orlistat 120 mg three times a day versus placebo | overweight or obese adults (BMI 28-40 kg/m(2)) with type 2 diabetes treated with insulin alone or combined with oral agents, but with suboptimal metabolic control (HbA(1c) 7.5-12.0%) | double-blind Follow-up duration: 1-year |
| Krempf, 2005 | orlistat 120 mg three times daily versus placebo | otherwise healthy, overweight patients aged 18-65 y (BMI >or=28 kg/m2 | double-blind Follow-up duration: 18-month |
| Lindgarde, 2000 | orlistat 120 mg three times daily versus placebo | obese adults (body mass index 28-38 kg m-2) with type 2 diabetes, hypercholesterolaemia and/or hypertension | double-blind Follow-up duration: 1 year Sweden |
| Lucas, 2003 | versus | ||
| Micic, 1999 | orlistat 120 mg three times daily versus placebo | obese patients (BMI > or = 30 kg/m2) with hyperlipidemia (LDL-cholesterol > or = 4, 2 mmol/l) | double-blind Follow-up duration: 24 weeks |
| Miles, 2002 | 120 mg orlistat t.i.d. versus placebo | overweight and obese patients with suboptimal control of type 2 diabetes | double-blind Follow-up duration: 1 year |
| Muls, 2001 | orlistat 120 mg three times daily versus placebo | obese hypercholesterolemic patients, BMI between 27-40 kg/m2 and low-density-lipoprotein cholesterol, LDL-C, between 4.1-6.7 mmol/l | double-blind Follow-up duration: 24 week |
| Naumov, 2002 | orlistat versus diet alone | patients with stable angina pectoris concomitant with obesity and hyperlipemia | open |
| Reaven, 2001 | versus | ||
| Rissanen, 2001 | orlistat 120 mg three times daily versus placebo | healthy obese women | double-blind Follow-up duration: 12-month |
| Rosenfalck, 2002 | versus | obese patients | |
| Rossner, 2000 | orlistat (60 or 120 mg) three times a day versus Obese patients (body mass index 28 to 43 kg/m2) | Obese patients (body mass index 28 to 43 kg/m2) | double-blind Follow-up duration: 2-year |
| Shi Yi, 2001 | versus | ||
| Sjostrom, 1998 | orlistat 120 mg (three times a day) versus | double-blind Follow-up duration: 1 year Europe | |
| Vidgren, 1999 | 120 mg of orlistat three times a day versus placebo | obese subjects | Follow-up duration: 1 year |
| PHEN/TPM high dose versus placebo | |||
| CONQUER (high-dose) (OB 303), 0 NCT00553787 | PHEN/TPM 15/92 mg versus placebo | Follow-up duration: 56 weeks | |
| OB 301 (high-dose), 0 | PHEN/TPM 15/92 mg versus placebo | Follow-up duration: 28 weeks | |
| OB 302 (high-dose), 0 | PHEN/TPM 15/92 mg versus placebo | Follow-up duration: 56 weeks | |
| PHEN/TPM low-dose versus placebo | |||
| OB 302 (low-dose), 0 | PHEN/TPM 3.75/23 mg versus placebo | Follow-up duration: 56 weeks | |
| PHEN/TPM mid-dose versus placebo | |||
| CONQUER (mid-dose) (OB 303), NCT00553787 | PHEN/TPM 7.5/46 mg versus placebo | Follow-up duration: 56 weeks | |
| OB 301 (mid-dose), 0 | PHEN/TPM 7.5/46 mg versus placebo | Follow-up duration: 28 weeks | |
| sibutramine versus placebo | |||
| SCOUT, 2010 NCT00234832 | sibutramine versus placebo | overweight or obese patients with diabetes or a history of coronary or peripheral vascular disease or stroke, along with other CV risk factors | double blind Follow-up duration: 3.4 year |
| Sibutramine versus placebo | |||
| McMahon, 2002 | versus | ||
| McMahon, 2000 | versus | ||
| Smith, 2001 | versus | ||
| tesofensine versus placebo | |||
| Astrup, 0 | versus | ||
| Topiramate versus placebo | |||
| Bray, 2003 | versus | ||
| Caterson, 2003 | versus | ||
| Pud’homme, 2003 | versus | ||
| Rissanen, 2003 | versus | ||
| Stenlof, 2003 | versus | ||
| Tonstad, 2003 | versus | ||